TW567686B - Method and apparatus for cell search for W-CDMA - Google Patents

Method and apparatus for cell search for W-CDMA Download PDF

Info

Publication number
TW567686B
TW567686B TW91107676A TW91107676A TW567686B TW 567686 B TW567686 B TW 567686B TW 91107676 A TW91107676 A TW 91107676A TW 91107676 A TW91107676 A TW 91107676A TW 567686 B TW567686 B TW 567686B
Authority
TW
Taiwan
Prior art keywords
stage
code
cell search
patent application
scope
Prior art date
Application number
TW91107676A
Other languages
Chinese (zh)
Inventor
Wern-Ho Sheen
Jan-Shin Ho
Original Assignee
Accton Technology Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Accton Technology Corp filed Critical Accton Technology Corp
Priority to TW91107676A priority Critical patent/TW567686B/en
Application granted granted Critical
Publication of TW567686B publication Critical patent/TW567686B/en

Links

Landscapes

  • Synchronisation In Digital Transmission Systems (AREA)

Abstract

The invention discloses a cell search method for the CDMA system, using three stage cell search. The method comprises the steps of: matching an incoming signals from the basestation; over-sampling the incoming signals N times against a chip rate and outputting N over-samples (Y1(k), Y2(k), ... YN(k)); down-sampling the incoming signals and outputting the N over-samplers to N parallel signal paths, and proceeding the N over-samples serially in a first stage process, a second stage process and a third stage process to accomplish a trial; wherein the N over-samples are used differently in the first stage process, the second stage process and the third stage process controlled by a control process. A cell search method of the present invention can be used for reducing simultaneously the effects of non-ideal sampling and clock offset, and to accomplish fast cell search. Another, the invention also discloses a cell search apparatus for realizing the cell search apparatus under the effects of non-ideal sampling and clock offset in the system without increasing the hardware complexity.

Description

567686 五、發明說明α) 【發明領域】 本發明係有關於一種用於分碼多工接取系統(C 〇 d e division multiple access,CDMA)之細胞搜尋方法及裝 置,更特別有關於一種用於寬頻分碼多工接取(wi deband code division multiple access’ W-CDMA)系統之細胞搜 尋方法及裝置,該方法及裝置能同時降低系統中非理想取 樣效應與取樣頻率偏移的效應(the effects of clock offset)0 【先前技術】 使用一直接序列型展頻分碼多工接取(direct sequence spread spectrum code division multiple access)技術 的分碼多工接取細胞式系統(c e 1 1 u 1 a r s y s t e m s )大幅地增 加通道容量。該系統於最近之行動通訊系統研究中吸引相 當之注意。一般而言,由於頻率的再利用(freqUenCy reuse)性質,分碼多工接取系統之頻寬效率(bandwidth ef f iciency )比起其他多工接取系統(如分頻多工接取與 時多工接取)更加優越。此外,細胞規劃(cel丨-在分碼多工接取系統係相當簡單。因此,分碼多工接取細 胞糸統將疋未來之主流。特別是第三代合作計畫(T h i r d generation partnership project,3GPP)寬頻分碼多工567686 V. Description of the invention α) [Field of the invention] The present invention relates to a cell search method and device for a code division multiple access system (CDMA), and more particularly to a method for searching for cells. Cell search method and device of wide band division multiple access (W-CDMA) system, the method and device can reduce the effects of non-ideal sampling and sampling frequency offset in the system at the same time of clock offset) 0 [Previous technology] A ce 1 1 u 1 arsystems using a direct sequence spread spectrum code division multiple access technology ) Significantly increase channel capacity. This system has attracted considerable attention in recent research on mobile communication systems. Generally speaking, due to the nature of frequency reuse (freqUenCy reuse), the bandwidth efficiency (bandwidth ef f iciency) of the code division multiplex access system is higher than that of other multiplex access systems (such as frequency division multiplex access and time). Multiple access) is even better. In addition, cell planning (cel 丨-multiplexing access system is quite simple. Therefore, the multiplexing access system will be the mainstream of the future. Especially the third generation partnership plan (Third generation partnership project, 3GPP) Wideband Code Division Multiplexing

接取/分頻雙工(¥-00^^/?00)系統已被採用於一種用於 IMT-2 0 0 0第三代系統的標準之一。 在一分碼多工接取之細胞式系統中,被用戶裝置(u s e r equipment,UE)作為搜尋最佳細胞的方法係被稱為”細胞The access / division duplex (¥ -00 ^^ /? 00) system has been adopted as one of the standards for IMT-2 0 0 0 third generation systems. In a cellular system with one-code multiplex access, the user equipment (UE equipment, UE) as the method to search for the best cell is called "cell"

第6頁 567686 五、發明說明(2) * 搜尋’’(c e 1 1 s e a r c h)。快速的細胞搜尋係非常重要,為了 減少該用戶裝置開機延遲時間(sw i tched-on de 1 ay )(初始 搜尋)、增加待機(standby time)(閒置狀態搜尋)及在換 手(handover)(動作狀態搜尋,active mode search)保持 良好的通訊連結品質。 見於頒給Shou等人之美國專利號碼第6, 0 38, 25 0號,其 標題為”初始化同步方法及直接序列型之分碼多工接取中 繼台非同步細胞系統的接收器”(I n i t i a 1 Synchronization Method And Receiver for DS-CDMA Inter Base Station Asynchronous Cellular System ) 揭示一使用初始化同步方法於高速被搜尋之細胞及一接收 器用於直接序列型之分碼多工接取中繼台非同步細胞系 統。一基頻帶接受訊號被輸入至一匹配濾波器且相關於一 展頻碼,該展頻碼由展頻碼產生器提供。一訊號電功率計 算器計算匹配濾波器的相關輪出之電功率,且輸出該結果 至長碼同步時程决疋裔(long code synchroniziation timing determiner)、門攔值計算器(thresh〇ld value&V calculator)及長碼驗證器(1〇ng code identifier)。於 初始細胞搜尋期間’該展頻碼產生器輸出一短碼,該短碼 係共同於每一基地台之控制通道。長碼同步時程已被決定 之後,每一組成一部分合成展頻碼序列之N碼片的碼片係 相繼被置換與輸出。 見於頒給Nystrom等人之美國專利號碼第6, 1 85, 244號, 其標題為”細胞搜尋於分碼多工接取通訊系統,,(Ce i 1Page 6 567686 V. Description of the invention (2) * Search for '' (c e 1 1 s e a r c h). A fast cell search system is very important. In order to reduce the user device's turn-on delay (initial search), increase standby time (idle search), and handover ( Active mode search) maintains good communication link quality. See U.S. Patent No. 6, 0 38, 2500 issued to Shou et al., Whose title is "Initialization of Synchronization Method and Direct-Sequence Code Division Multiplexing Access Receiver for Asynchronous Cell System Receiver" ( I nitia 1 Synchronization Method And Receiver for DS-CDMA Inter Base Station Asynchronous Cellular System) Reveals an initialization synchronization method for high-speed searched cells and a receiver for direct-sequence-based multiplexing access relays asynchronous Cell system. A baseband acceptance signal is input to a matched filter and is associated with a spreading code provided by a spreading code generator. A signal electric power calculator calculates the relevant round-out electric power of the matched filter, and outputs the result to a long code synchroniziation timing determiner, a threshold value & V calculator ) And long code identifier (10ng code identifier). During the initial cell search period, the spread-spectrum code generator outputs a short code which is common to the control channel of each base station. After the long code synchronization schedule has been determined, each chip of the N chips that make up a part of the synthesized spreading code sequence is successively replaced and output. See U.S. Patent No. 6, 1 85, 244, issued to Nystrom et al., Entitled "Cell Search in Code Division Multiplexing Access Communication System," (Ce i 1

第7頁 567686 五、發明說明(3) searching in a CDMA communications system)’ 揭示於 細胞搜尋於分碼多工接取通訊系統期間,更有效率之編碼 計晝需要一長碼及碼框時程。一個具有M Q列(M Q-ary)碼 字長度的碼集合,其中該碼字包含來自一 Q短碼的集合, 該碼集合係定義至特定的特性。該被滿足的初始特性為該 碼字無循環性飄移因而產生一有效之碼字;其他的被滿足 的特性為於長碼訊息與有效之碼字之間,具有一對一應稱 (m a p p i n g),且該編碼器將可發現出現在干擾與雜訊之隨 機移動(因而發現碼框時程)與該傳輸的碼字(亦即,相關 於長碼表示 息(long code indication message)),具 有某些程度上的精確與合理的複雜度。 見於頒給K i m等人之美國專利號碼第6,2 8 9,0 0 7號,其標 題為π —個在非同步分碼多工接取行動通訊系統之獲得搜 哥細胞基地台的方法,’(Method for Acquiring A Cell Site Station in Asynchronous CDMA CellularPage 7 567686 V. Description of the invention (3) searching in a CDMA communications system) 'Reveals that during cell search during a multiplexed multiplex access communication system, a more efficient coding schedule requires a long code and frame time schedule. . A code set with an M Q-ary codeword length, where the codeword includes a set from a Q short code, the code set is defined to a specific characteristic. The satisfied initial characteristic is that the codeword has no cyclic drift and thus generates a valid codeword; other satisfied characteristics are that there is a one-to-one mapping between the long code message and the valid codeword. And the encoder will be able to detect random movements that occur in interference and noise (hence the time frame of the code frame) and the transmitted codewords (ie, related to long code indication messages), with Some degree of precision and reasonable complexity. See U.S. Patent No. 6, 28.9, 07, issued to Kim et al., With the title π-a method for obtaining a Sogo cell base station in a non-synchronous multiplexing mobile communication system , "(Method for Acquiring A Cell Site Station in Asynchronous CDMA Cellular

Communication Systems),揭示一群碼(group code)與; 胞碼係多工傳輸的且被用作為一引導碼(p i 1 〇 t c 〇 d e ), 引導碼用於非同步細胞分碼多工接取通訊系統中之有差別 的基地σ 。使用夕工傳輸碼’干擾由於使用兩個引導碼而 減少。一個在非同步分碼多工接取行動通訊系統之獲得搜 哥細胞基地台的方法包含一基地台控制器、複數個行動台 及基地台、和使用不同序列之不同基地台,該搜尋細胞^ 地台的方法之步驟包含(a )指定該細胞之群碼作為基地台 的同相(inphase )通道之引導碼(b )指定該細胞之群碼作為Communication Systems), revealing a group code and cell code are multiplexed and used as a pilot code (pi 1 〇tc 〇de), the guide code is used for asynchronous cell division code multiplexed access communication There are different bases σ in the system. The use of the evening transmission code 'interference is reduced due to the use of two pilot codes. A method for obtaining a search cell base station in a non-synchronous code division multiplexed mobile communication system includes a base station controller, a plurality of mobile stations and base stations, and different base stations using different sequences. The search cell ^ The steps of the floor method include (a) designating the cell code of the cell as the guide code of the inphase channel of the base station (b) designating the cell code of the cell as

567686 五、發明說明(4) 基地台的四分之一(quadra ture)通道之引導碼(c)多工傳 輸該同相(inphase )通道與四分之一(quadrature )通道之 引導碼及產生一同相與四分之一之引導碼。567686 V. Description of the invention (4) The pilot code of the quadrature channel of the base station (c) Multiplex transmission of the pilot code of the inphase channel and the quadrature channel and generation together Matches a quarter of the boot code.

現請參考第一圖,該圖將有助於了解一第三代合作計晝 (3 G P P)見頻分碼多工接取/分頻多工系統之碼框結構 (frame structure)。首先,在第三代合作計晝(3gpp)之 寬頻分碼多工接取/分頻多工系統中,細胞搜尋係典型上藉 由三個階段(three stages)來完成,該三階段係包含兩個 特別設計的同步通道(synchronization channel,SCH)及 一個共同引導通道(common pilot channel,CPICH)。在 弟一階段110中’初級同步通道(primary synchronization channel,PSCH)111 係用於時槽(slot) 同步。该初級同步通道111包含有初級同步碼(primary synchronization code,PSC)定義為 aCp,其中 ”a” (=± 1 )係依賴在基地台傳送的多樣性傳送(diversity transmission)存在與否而定。在第二階段12〇中,次級_ 步通道(secondary synchronization channel,SSCH)12l 係用於碼框/碼群(frame/code group)辨識。該次級同步 通道121係包含有次級同步碼(secondary synchronization code,SSCs)定義為 acs,其中係數3係Please refer to the first figure, which will help to understand the frame structure of a third-generation cooperative computing day-to-day (3 G P P) system. First, in the third-generation cooperative computing day-to-day (3gpp) wideband code division multiplexed access / frequency division multiplexed system, the cell search system is typically completed by three stages, which include Two specially designed synchronization channels (SCH) and a common pilot channel (CPICH). In the first stage 110, the 'primary synchronization channel (PSCH) 111 is used for slot synchronization. The primary synchronization channel 111 includes a primary synchronization code (PSC) defined as aCp, where “a” (= ± 1) depends on the presence or absence of diversity transmission transmitted at the base station. In the second stage 120, a secondary synchronization channel (SSCH) 12l is used for frame / code group identification. The secondary synchronization channel 121 contains secondary synchronization codes (SSCs) defined as acs, where the coefficient is 3

等同於初級同步通道之係數。在第三階段1 3 0中,該共同 引V通道131係用於下傳擾|匕碼(downlink scrambling c o d e )之決定。如圖所示,在1 〇毫秒(m s )碼框中包含了 1 5 個時槽,並且因為在該系統中使用每秒3. 8 4百萬碼片Coefficient equivalent to the primary synchronization channel. In the third stage 130, the common V channel 131 is used for the decision of downlink scrambling co o de e. As shown in the figure, 15 time slots are included in the 10 millisecond (ms) code frame, and because 3.84 million chips per second are used in this system

第9頁 567686 五、發明說明(5) (Mchips/sec)的速度。因此,每一碼框中包含3840 0個石馬 片,也就是每一時槽中包含2 5 6 0個碼片。此外,該初級同 步通道與該次級同步通道長度係包含2 5 6個碼片且僅在言亥 時槽邊界的開端傳輸。 用於第三代合作計畫(3GPP)之寬頻分碼多工接取/分頻 多工系統之傳統的細胞搜尋可被分為兩種概括的種類:依 序式(serial)搜尋及導管式(pipelined)搜尋。如圖二所 示,依序式搜尋在下一個新的搜尋開始之前,需要依序經 過三個同步階段,分別為(1 )時槽同步(s 1 〇 t s y n c h r ο n i z a t i ο η ) ( 2 )碼框同步 /碼群判定(framePage 9 567686 V. Description of the invention (5) (Mchips / sec) speed. Therefore, each code box contains 3840 pieces of stone horses, that is, each time slot contains 2560 pieces of chips. In addition, the length of the primary synchronization channel and the secondary synchronization channel include 256 chips and are transmitted only at the beginning of the slot boundary. The traditional cell search for the 3rd Generation Partnership Project (3GPP) wideband code division multiplexed access / frequency division multiplexed system can be divided into two general categories: serial search and ducted (Pipelined) search. As shown in Figure 2, before the next new search starts, the sequential search needs to go through three synchronization stages in sequence, which are (1) time slot synchronization (s 1 〇tsynchr ο nizati ο η) (2) code frame Synchronization / code group decision

synchronization/code group identification)(3)擾亂 碼判定(scrambling code identification)。現請參考第 一(a)圖’違圖係一用於傳統三階段依序式(s e r i a 1)細胞 搜尋過程之簡化圖。為簡化起見,一完整的三階段搜尋將 被稱之為一個試驗(t r i a 1)。在依序式細胞搜尋中,試_ 並不重疊,直到該搜尋成功為止,也就是說,在一時間 只能有一個階段在動作,即一時間内只有一個方框 ’〜: (匕1(^1〇21卜方框212與方框213在動作(此處每一方框表 示某一試驗的某一階段),因此消耗較低的功率損失,但 花費更長的搜尋時間。 此外,如第二(b)圖所示,導管式㈧丨^丨丨^诚尋之三 個階段則分別同時進行。為詳細介紹導管式搜尋,該圖係 二用於,統三階段導管式細胞搜尋過程法之簡化圖。在導 管式搜尋中,不同階段之檢測係同時操作,也就是說試驗synchronization / code group identification) (3) scrambling code identification. Please refer to the first (a) diagram. The violation diagram is a simplified diagram for the traditional three-stage sequential (s e r i a 1) cell search process. For simplicity, a complete three-stage search will be referred to as an experiment (t r i a 1). In sequential cell search, try_ does not overlap until the search is successful, that is, there can be only one phase in action at a time, that is, there is only one box in a time '~: (dagger 1 ( ^ 1021 Boxes 212 and 213 are in action (each box represents a certain stage of a test), so it consumes lower power loss, but takes longer search time. In addition, as As shown in Fig. 2 (b), the three stages of catheter-type ㈧ 丨 ^ 丨 丨 ^ are performed simultaneously. In order to introduce the catheter-type search in detail, the figure is used for the three-stage catheter-type cell search process. Simplified diagram. In the catheter search, the detection at different stages is performed simultaneously, that is, the test

第10頁 567686 五、發明說明(6) 與 試驗v之間係重疊的。舉例來說,方框3 11、方框3 2 1與方 框3 3 1係在同一個試驗。明顯的,在導管式搜尋中,在一 個固定的,間内可以有更多可能的試驗,也因此得到一個 更快之搜尋。當然所付出之代價係更大之功率銷耗。為了 加速ί胞搜尋’因此,該導管式搜尋較廣泛為人所使用。 1注意對導管式搜尋而言,比起依序式細胞搜尋並沒有額 =的硬體裝置係需要的。舉例來說,若我們假設每一階段 需I ϊ 秒ί時間,如果該細胞搜尋在第K次試驗成功, ,母一次搜尋所需要的細胞搜尋時間係(κ + 2)χ 1〇毫秒 (=);相較之下依序式搜尋則需要b 3〇毫秒(μ)。 八=^,一般使用於第三代合作計畫寬頻分碼多工接取/ 1 工之細胞搜尋之先前技術中有兩個基本假設。第 碼片''匹配渡波器(chi p-matched fi Iter)輸出之取 的(理想取樣)。然而,實際上,在碼片—匹配濾 菸t =之取樣係不是完美的(即非理想取樣)。第二,d 碼片時間對接收機係已精確知道(即是沒有取抓' ίίΐίiciock drift or ci〇ck 也就是,該 =Ϊ f 率係皆設定沒有頻率之偏移。實際上,頻 ί ΐ i offset)係來自於用戶裝置之晶體震盡 ϊΐΐίϊΞΓ對用戶裝置而$,該進入信號載波頻率 ί 頻率偏移,其中取樣頻率偏移的部 # _ / ΐ ΪIί未被考慮到。該頻率偏移造成的取樣 員丰偏和存在於基地台與用戶裝置之間。現請參考表一,Page 10 567686 V. Description of the invention (6) and test v overlap. For example, Box 3 11, Box 3 2 1 and Box 3 3 1 are in the same test. Obviously, in ducted search, there are more possible trials in a fixed, in-room, and therefore a faster search. Of course, the price paid is greater power consumption. In order to speed up cell search ', this catheter search is more widely used. 1 Note that for catheterized searches, hardware devices are not required compared to sequential cellular searches. For example, if we assume that each stage takes 1 ϊ seconds, and if the cell search succeeds in the Kth test, the cell search time required for a mother search is (κ + 2) x 10 milliseconds (= ); In contrast, a sequential search requires b 30 milliseconds (μ). Eight = ^, there are two basic assumptions in the prior art generally used in the third-generation cooperative project wideband code division multiplexed access / 1-cell cell search. The chip "chi p-matched fi Iter" output (ideal sampling). However, in practice, the sampling system at chip-matched filter t = is not perfect (ie, non-ideal sampling). Second, the d chip time has been accurately known to the receiver system (that is, no fetching or catching). That is, the = Ϊ f rate is set without a frequency offset. In fact, the frequency ί ΐ i offset) is derived from the crystal of the user device. The frequency of the incoming signal carrier frequency is frequency offset, and the part of the sampling frequency offset # _ / ΐ ΪI is not taken into account. This frequency offset causes sampler abundance to exist between the base station and the user device. Please refer to Table 1.

第- 567686 五、發明說明(7) 該表顯示在不同頻率偏移的狀況下所產生的取樣頻率偏 $,舉例來說,在12kHz頻率偏移的出現下,在一個3〇毫 秒碼框中會有〇· 69倍碼片時間的偏移,相當於6ppm的取樣 f f偏移。因此將造成誤差資訊及增加細胞搜尋時間。在 ^月中’我們較著重於解決該頻率偏移量小於6ppm的狀 況’但本發明並不受限於此。 曰第二(a)圖與第三(b)圖並非先前技術,但係發明人在考 f頻率偏移造成的碼片偏移時間效應下在初級碼匹配濾波 為輸出的觀察圖。如第三(㈧圖與第三(b)圖顯示,由於頻 率偏移所造成之取樣頻率偏移效應下,信號位準降低與碼 片間干擾增加的結果。 【發明概要】 本發明之主要目的係提供一種細胞搜尋方法,用於分碼 多工接取系統,更特別係用於寬頻分碼多工接取系統,可 以使用於降低系統中非理想取樣效應與取樣頻率偏移效應 並快速完成細胞搜尋。 ,於分爹 糸統,在 下實現細 本發明之次要目的係提供一種細胞搜尋裝置, 多工接取系統,更特別係用於寬頻分碼多工接取 系統中具有非理想取樣效應與取樣頻率偏移效應 胞搜尋裝置,且不增加硬體的複雜度。 為達上述之主要目的,本發明提供一種細胞搜尋方法, 用於分碼多工接取系統,更特別係用於寬頻分碼多工接取 系統,降低非理想取樣效應與取樣頻率偏移效應下。其 第一階段具有一初級同步通道(P S C Η )係用於時槽同步;第Article-567686 V. Description of the invention (7) The table shows that the sampling frequency generated under different frequency offsets is $, for example, in the presence of a 12kHz frequency offset, in a 30 millisecond code box There will be an offset of 0.69 times the chip time, which is equivalent to a sampling offset of 6 ppm. This will cause error information and increase the cell search time. In the following month, 'we focus more on solving the case where the frequency offset is less than 6 ppm', but the present invention is not limited to this. The second (a) and third (b) diagrams are not the prior art, but are observation diagrams of the inventor's primary code matching filtering as the output under the consideration of the chip offset time effect caused by the f frequency offset. As shown in the third figure (㈧ and third (b)), under the sampling frequency shift effect caused by the frequency shift, the signal level is reduced and the inter-chip interference is increased. [Summary of the invention] The main features of the present invention The purpose is to provide a cell search method for code division multiplexing access systems, more specifically for wideband code division multiplexing access systems, which can be used to reduce non-ideal sampling effects and sampling frequency offset effects in the system and quickly Complete the cell search. To achieve the secondary purpose of the present invention, the secondary purpose of the present invention is to provide a cell search device, a multiplexed access system, and more particularly, a non-ideal system for a wideband multiplexed multiplexed access system. Sampling effect and sampling frequency offset effect cell search device without increasing the complexity of the hardware. In order to achieve the above-mentioned main purpose, the present invention provides a cell search method for a code division multiplexing access system, and more particularly used Under the wide-frequency division code multiplexed access system, the non-ideal sampling effect and the sampling frequency offset effect are reduced. The first stage has a primary synchronization channel (PSC Η) for Slot synchronization; a first

567686 五、發明說明(8) 二階段具有次級同步通道(SSCH)係在時槽同步 、 框/碼群辨識;且第三階段具有共同引導通V ^ ’用於碼 於擾亂碼之判定。根據本發明,該方法包含(,PICH)係用 配(match)來自基地台之一進入信號;將該進列〜步^驟、·匹 碼片速率過取樣N次並輸出過取樣之_取^樣入/號以一 Y2〇〇、、、YN(k));將該進入信號降取樣且^^」(1°’ 樣點至N條平行信號路徑;將該n個過取樣點:出該N個取 階段處理,一第二階段處理及一第三段;依序作一第一 試驗(t r i a 1 );其中藉由一控制過程,該==以完成一個 第一階段處理,該第二階段處理及該第三樣點在該 不同的使用。 —^ #又處理中係有 该細胞搜尋之該試驗更包含下列步驟·# 中,可得到該進入信號之一時槽同步;,弟一階段處理 中,檢測該進入信號之一碼群與碼框同步·二,,處理 理中,選擇該進入信號之一擾亂$;兮2三階段處 欄值”。作一第一認證;其中如果該擾,碼與一門 則所選之該擾亂碼進行一第二驗噔.J:將重新開始;% 過該第二驗證,則試驗係成功,否則如果該擾亂碼通 間T p毫秒(m s )後重新開始。 、4試驗在一延遲時 根據本發明之一特徵,直該 取樣點。 佩點中選取一最佳 根據本發明之另-特徵,其中該 制過程更包含下列步567686 V. Description of the invention (8) The second stage has a secondary synchronization channel (SSCH) which is synchronized in the time slot and frame / code group identification; and the third stage has a common guidance pass V ^ 'for the determination of the scrambled code. According to the present invention, the method includes (, PICH) matching an incoming signal from one of the base stations; over-sampling the sequence ~ steps, · chip rate N times and outputting the over-sampling ^ Sample input / number is a Y200 ,,, YN (k)); downsample the incoming signal and ^^ "(1 ° 'sample point to N parallel signal paths; the n oversampling points: Out of the N take-stage processing, a second-stage processing and a third-stage processing; a first test (tria 1) is performed in sequence; where by a control process, the == to complete a first-stage processing, the The second stage of processing and the third sample are used in different ways. — ^ #The experiment in which the cell is searched for in the process further includes the following steps. # One of the access signals can be time-slot synchronized; In the first stage of processing, it is detected that one code group of the incoming signal is synchronized with the code frame. Second, during processing, selecting one of the incoming signals disturbs the value of $; Xi 2 is the value at the third stage. As a first authentication; If the scramble code and a gate are selected, the scramble code selected will be subjected to a second check. J: will restart;% pass the second check The test is successful, otherwise, if the scrambled code passes between T p milliseconds (ms), the test is restarted. 4. At a delay, according to one of the features of the present invention, the sampling point is straightened. Select an optimal point. According to another feature of the present invention, the manufacturing process further includes the following steps:

第13頁 、發明說明(9) 、 :在第一階段處理中,在該 \ 取樣點,並傳送至第二階烟過取樣 在該試驗的三階段處理。 理及第=触ρ ^也%取 . 〜階枚處i里% ,以進 五 驟 一一 行 驟 係 根據本發明之一特徵,复中 “又處壞,^ :在第-階段處理、第二階J;制過程更包含卞 隨機且獨立地在該Ν個過取&處理及第三階段^巧蚩 該試驗的每一階段中處理。 點中選取〜取樣;硬時, 本發明亦提供一種細胞搜尋f Q在 統,更特別係用於寬頻分碼多^ ^,用於分碼多工 個階段之通道,其中第一階段具^系統,該裝置處理1 係用於時槽同步;第二階段具有:初級同步通道(psci) 時槽同步後,用於碼框/碼群辨識、、及同步通道(SSCH)係在 引導通道(CPICH)係用於下傳择礼碼且第三階段具有共同 一用於分碼多工接取系統之細夂胞^之決定。根據本發明 置包含:一碼片匹配濾波器,用号裝置,該細胞搜尋裝 入信號;一取樣元件Γ連二於詨碼,配來自基地台之一進 該進入信號以一碼片速率過取i 、匹配濾波器,用以, 樣點(Yi(k),Y2(k)、、、 ⑴人亚輪出過取樣之N個!^ 元用以輪出該心取點至一-降第取樣器,連結於該 二弟ϋ &檢測器及—第三階段檢卓一階段檢測器、 ;牛ϊ ί該降取樣器,用於得到今:;胃第-階段檢測 同步,该第二階段檢測哭,連社j j進入信號之之一時槽 ϊίϊΐί之—碼群與碼框同步;取樣器,用以得到 ,、、°至该产牛取樣器,用以決定該進入ΐί三階段檢測器,連 w現之一擾亂碼;一控Page 13 of the invention description (9): In the first stage of processing, at the \ sampling point, and transfer to the second stage of smoke oversampling in the three stages of the test. Reason and the first = touch ρ ^ also% take. ~ Steps at i li%, in order to enter five steps and one step is based on one of the features of the present invention, complex "is bad again, ^: in the first stage processing, The second-stage J; manufacturing process further includes: 卞 random and independent processing in the N over-fetching & processing and the third stage ^ cleverly in each stage of the test. Point selection ~ sampling; when hard, the present invention A cell search f Q system is also provided, more specifically for wideband code division and multiple channels, and for the channel of multiple code division stages. The first stage has a system. The device processes 1 system for time slots. Synchronization; the second phase has: primary synchronization channel (psci) time slot synchronization, used for code frame / code group identification, and synchronization channel (SSCH) is used in the pilot channel (CPICH) for downloading gift codes and The third stage has a common decision of a cell for a code division multiplexing access system. According to the present invention, a chip-matching filter is used, and the number device is used to search for a loading signal in the cell; a sampling element Γ is connected to the 詨 code, and one of the base stations enters the incoming signal to fetch i, Equipped with a filter for, sample points (Yi (k), Y2 (k) ,,, ⑴ren sub-round over-sampling N! ^ Yuan to round out the heart to the first-down sampler , Connected to the second brother & detector and the third-stage inspection first-stage detector, the cattle down the sampler, used to obtain :; stomach first-stage detection synchronization, the second-stage detection Cry, even when the jj enters one of the signals, the slot group is synchronized with the code frame. The sampler is used to obtain the sampler that is used to determine the entry to the three-stage detector. w now one scramble code; one control

第14頁 ^00 五二發明說明(10) _____ 制π件,連結至該第一階丰、、的 該第三階段檢測器,用以^二測為、、該第二階段檢測器及 段檢測器、該第二階段檢^該^個> 過取樣點在該第一階 同的使用;以及一認證單元為及該第三階段檢測器中作不 用於決定該試驗是否成功。’連結於該第三階段檢測器, 的該認證單元更包含··— 态,用以測試輸出自該第三比=,連結至該第三階段檢測 〇比較;一第一決定元件厂、1皆段之該擾亂碼與一門欄值77 5碼是否正確;其中如果該,二較器,以決定該 視為失敗,且一新試驗在 Λ ]襴值未被超過,則該試驗 果該門攔值被超過ν,則所S,遲了將重新開始,反之,如 證單元;該同步驗證單位,、疋之δ亥擾亂碼即進入一同步驗 驗證該擾亂碼;以及一第i連結至該第一決定元件,用以 單位,用以決定該擾亂碼元件,連接至該同步驗證 過該第二決定元件,則試1,受;其中如果該擾亂碼通 遲時間TP毫秒(IDS)後重二f二功,否則一新試驗在一^ 根據本發明之一特徵,复 ;k: 制元件之控制,在該細迅&中样該第一階段檢測器藉由金—控 根據本發明之ί特:過二樣二中選取-最佳取樣點。 制元件之控制,在哕_/亥第一階段檢測器藉由該控 點&彳t〜在^财固過取认點中隨機地選取一取樣 ;,以二谁运f該第二階段檢測器及該第三階段檢測 杰,以龜續進行該三階段之細胞搜尋。 根據本發明之一特徼,立φ益 第一階段檢測哭、該第_ ^ p ^由該控制元件之控制,該 口口 第一 P白&仏測器及該第三階段檢測Page 14 ^ 00 May 2nd invention description (10) _____ π-made pieces, connected to the first stage detector, the third stage detector, for the second stage detector, the second stage detector and section The detector, the second stage inspection, the ^ th > oversampling point are used in the first stage; and an authentication unit is used in the third stage detector to determine whether the test is successful. 'The authentication unit connected to the third-stage detector further includes a state for testing output from the third ratio =, which is connected to the third-stage detection and comparison; a first decision component factory, 1 Whether the scrambling code and a gate value of 77 5 yards are correct; if so, the two comparators determine that the failure is considered a failure, and a new test does not exceed the value of Λ] Λ, then the test results in the gate. If the blocking value is exceeded ν, S will be restarted if it is late, otherwise, such as the proof unit; the synchronous verification unit, the δ δ scrambling code will enter a synchronization verification to verify the scrambling code; and an i-th link to The first decision element is a unit for determining the scramble code element, and is connected to the second verification element that has been synchronously verified, then try 1 and accept; wherein if the scramble code delay time is TP milliseconds (IDS) Duplicate two f two work, otherwise a new test in one ^ According to a feature of the present invention, complex; k: control of control elements, in the fine & the first stage detector by gold-control according to the present The special feature of the invention: Select the best sample point in the second sample. The control of the control element, in the first stage of the __ / hai the detector uses the control point & 彳 t ~ randomly select a sample in the ^ Caiguo pass recognition point; to two who run f the second stage The detector and the third-stage detection kit continue to perform the three-stage cell search. According to a feature of the present invention, the first phase detection is performed, and the first phase detection is controlled by the control element, the first phase white detector and the third phase detection.

器’係隨機且獨立地在該N個 以在各階段檢測器中處理。 從下文詳細的描述 易見。 s c h e m e )。若系統中同時具有非理想取樣效應與取樣頻率 偏移效應,則該控制過程應將細胞搜尋方法導入一隨機取 樣策略(random sampling scheme)中。在裝置的實現上, 所附圖Detectors are randomly and independently processed in the N detectors at each stage. It is easy to see from the detailed description below. s c h e m e). If the system has both non-ideal sampling effect and sampling frequency offset effect, the control process should introduce the cell search method into a random sampling scheme. In the implementation of the device, the attached drawings

567686 過取樣點中選取一取樣點, 本發明之其他特徵與優點將 示和所界定的專利範圍而顯而 【發明詳細說明】 第四,,使用本發明之一種細胞搜尋方法之一控制 過程1由於本發明之方法與裝置係同時考量到系統中非理 想取樣效應與取樣頻率偏移效應。因此,本發明提供不同 實施例以適用於不同的狀況下。如圖,若系統中具有非理 想取樣效應但沒有取樣頻率偏移效應,則該控制過程應將 細胞搜哥方法導入一預選擇策略(pre— selecti〇n 該控制過程可由一控制元件來擔任。 弟五圖係顯示根據本發明第一實施例之一種細胞搜 法,該方法係使用預選擇策略,或說是第一階段依序Ί試 (serial test in stage-1,STS1)方法。如第五圖所示, 每一方框表示某一試驗的某一階段,舉例來說,方框5 i丄 係表示第一階段處理,方框5 2 1係表示第二階段處理及方 框5 3 1係表示第三階段處理。根據本發明,總數個5 1 2擾亂 碼係被使用於下傳時之不同的細胞中,且係在整個系統中 重複使用。該碼又被細分為6 4群,每個群有8個碼。每個 碼框係3 8 4 0 0個碼片長且係因此擴展到整個碼框。由於該567686 Select a sampling point from the oversampling points. Other features and advantages of the present invention will be revealed by the patent scope defined by the invention. [Detailed description of the invention] Fourth, a control process using a cell search method of the present invention 1 Because the method and device of the present invention consider the non-ideal sampling effect and sampling frequency offset effect in the system at the same time. Therefore, the present invention provides different embodiments applicable to different situations. As shown in the figure, if the system has a non-ideal sampling effect but no sampling frequency offset effect, the control process should introduce the cell search method into a pre-selection strategy (pre-selection). The control process can be performed by a control element. The fifth figure shows a cell search method according to the first embodiment of the present invention, which uses a pre-selection strategy, or a serial test in stage-1 (STS1) method. As shown in the five figures, each box represents a certain stage of a certain test. For example, box 5 i represents the first stage of processing, box 5 2 1 represents the second stage of processing and box 5 3 1 The system represents the third stage of processing. According to the present invention, a total of 5 1 2 scrambling codes are used in different cells at the time of downloading, and are reused throughout the system. The code is subdivided into 6 4 groups, Each group has 8 codes. Each code frame is 3 384 chips long and is therefore extended to the entire code frame.

第16頁 567686 五、發明說明(12) - 細胞位置,不同步,該碼總是在該碼框邊界處開始其新的 週期。如第五圖所示,該方法中處理三個階段處理的過 程’在此描述其各階段處理之特徵。第一階段5丨〇内,具 有一初級同步通道(PSCH)係用於時槽同步。藉由使用相同 之初級同步通道於每一次搜尋且藉由僅傳送初級同步通道 在時槽邊緣,時槽同步可以被輕易地達到,藉由同步至該 初級同步通道。更甚者,一般化階級制度的葛雷序列 (generalized hierarchical Golay sequence)由於易於 實現,係被使用作為該初級同步碼。第二階段5 2 〇具有次 級同步通道(SSCH)係在時槽同步後,用於碼框/碼^辨人 識。同步與碼群辨識可以藉由檢測該次級同步通道而達 到,其中該碼群係被1 6個正交展頻碼之一個所展頻,稱之 為次級同步碼。為了減少相互干擾,該次級同步碼係正交 於該初級同步碼。此外,為實現快速之碼框/碼群辨識, 該次級同步通道更進一步被編碼成一組6 4碼字,藉由一 (1 5,3 )之無間斷里德-所羅門碼(c 〇 in m a - f r e e R e e d p Solomon code,CFRS),其中該組之每一碼字被表成土碼 群。因為無間段之良好特性,一旦碼群被指定,則該碼框 同步係完成。第三階段5 3 0具有共同引導通道 (cp丨fjj ^系 用於下傳擾亂碼之判定。在該碼群被指定後,藉由選擇二 群中8個碼之一個,經由使用共同引導通道,該胃擾礼碼係 可簡單地被決定。 ' 第六圖係顯示根據本發明第一實施例之一種細胞搜尋方 法之流程圖,該方法係使用第一階段依序測試方法。在步Page 16 567686 V. Description of the invention (12)-Cell position, not synchronized, the code always starts its new cycle at the border of the code frame. As shown in the fifth figure, the process of processing three stages in the method 'describes the characteristics of each stage of processing. Within the first stage, a primary synchronization channel (PSCH) is used for time slot synchronization. By using the same primary synchronization channel at each search and by transmitting only the primary synchronization channel at the edge of the time slot, time slot synchronization can be easily achieved by synchronizing to the primary synchronization channel. Moreover, the generalized hierarchical Golay sequence of the generalized class system is used as the primary synchronization code because it is easy to implement. The second stage 5 2 0 has a secondary synchronization channel (SSCH) which is used to identify the frame / code after the time slot synchronization. Synchronization and code group identification can be achieved by detecting the secondary synchronization channel, where the code group is spread by one of the 16 orthogonal spreading codes, which is called the secondary synchronization code. To reduce mutual interference, the secondary synchronization code is orthogonal to the primary synchronization code. In addition, in order to achieve fast frame / code group identification, the secondary synchronization channel is further encoded into a group of 64 code words, with a (1,5,3) uninterrupted Reed-Solomon code (c 〇in ma-free Reedp Solomon code (CFRS), where each codeword of the group is represented as a soil code group. Because of the good characteristics of the interval, once the code group is specified, the synchronization of the code frame is completed. The third stage 5 3 0 has a common guidance channel (cp 丨 fjj ^ is used to determine the transmission of scrambled codes. After the code group is designated, by selecting one of the 8 codes in the two groups, the common guidance channel is used. The gastrointestinal code can be simply determined. 'The sixth diagram is a flowchart of a cell search method according to the first embodiment of the present invention, which uses the first stage sequential testing method.

567686 五 驟 將 表 入 在 取 、發明說明(13) _______ 6 0 0中,檢測來自基地台之一、 該進入信號以碼片速率、馬 進入信號。在步驟6 1 0中, 示成YKk), Y2(k)、、义取樣知欠,且該過取樣後信號 信號降取樣且輸出該咖\^(1〇°在步驟615中,將該進 步驟6 2 0中,進行第_ 1取樣點至N條平行信號路徑。 一最佳取樣點,其中誃白N&處理,在該_過取樣點中選 沒有干擾出現下,係在=取樣點中之該最佳取樣點在 值。在第一階段處理中f 取樣點中具有最大的取樣 段之時槽同步。一非同% =取佳取樣點係用於得到第一階 其中該匹配濾波器係分=,#(Π〇η —coherent)匹配濾波器, 係以其絕對值合併,係個區段,且每-區段之輪出 第一階段中作為時槽成四個區塊且作為一被使用在 15時槽係被適當地發器。非,的累積超過 Γ . ·、 馬白色咼斯雜訊(additivewhite567686 Five steps are listed in the fetching, invention description (13) _______ 6 0 0, to detect from one of the base stations, the incoming signal at the chip rate, the horse incoming signal. In step 6 10, it is shown as YKk), Y2 (k), and the sense sampling is insufficient, and after the oversampling, the signal signal is down-sampled and the result is output. (In step 615, the In step 6 2 0, the _1 sampling point to N parallel signal paths is performed. An optimal sampling point, in which N & processing is performed, is selected in the _oversampling point without interference, and is tied to = sampling point. The best sampling point is in the value. In the first stage of processing, the time slot with the largest sampling segment in the f sampling points is synchronized. A different% = the best sampling point is used to obtain the first order where the matched filtering The device is divided into #, # (Π〇η —coherent) matched filters, combined with their absolute values, and are divided into sections, and each-section turns out into four blocks as time slots in the first stage and As one is used at 15 o'clock, the slot system is properly fired. The accumulation of non, exceeds Γ. ·, Horse white noise (additive white

baussiannoise)0 為了 击工从 ^ u , L _ , A 1 『車父佳的特性,弟一階段中超過一 個時槽的邊界被選擇谁λ t τ 卜 ^ Τ釉J过I f 、伴進入下_個階段。第一階段處理中, 在該_過取樣點中選取—畀从&冰科难田彳 、 、立 敢佳取樣點使用Nx 1 0笔 、)。^且需注思’本發明實施例所用之方法係如圖 所述,藉由一控制過程,該N個過取樣點在該第一階段處 理’該第二階段處理及該第三階段處理中係有不同的使 用。 #不二β T又缛理中完成。該第二階段處理,使 用1 6個匹配)慮波為去檢測該次級同步碼。在第二階段之該 在步驟6 3 0中,該最佳取樣點傳進行第二階段處理與第 階段處理。在步驟6 4 〇中,在時槽同步後,該碼群與碼 框同步可以在第一 P&段處理中完成。該第二階段處理,使 [Jm nr :忐、、士 笼土 4人、…baussiannoise) 0 In order to strike from ^ u, L _, A 1 『Characteristics of the car ’s father, who is more than one time slot boundary in the first stage is chosen who λ t τ bu ^ glazed J over I f _ Stages. In the first stage of processing, select from this _ oversampling point-畀 from & Bingke Nantian 立, Li Ningjia sampling point using Nx 10 pen,). ^ It should be noted that the method used in the embodiment of the present invention is as shown in the figure. With a control process, the N oversampling points are processed in the first stage, the second stage process and the third stage process Departments have different uses. # 不二 β T is done in the middle again. In the second stage of processing, 16 matchings are used to detect the secondary synchronization code. In the second stage, in step 630, the optimal sampling point is transmitted for the second stage processing and the first stage processing. In step 64, after the time slot synchronization, the code group and code frame synchronization can be completed in the first P & segment processing. This second-stage treatment makes [Jm nr: 忐 ,, Shi Cangtu 4 people, ...

567686 五、發明說明(14) 同調的累積(the coherent accumulation)係可能的籍由 使用來自第一階段之該通道估計。在集合了 1 5個次級同少 碼後,它們係相關於該6 4無間斷里德-所羅門碼 (comma-free Reed Solomon code,CFRS)碼字,每一石馬字 有1 5可能的循環移動位置。如此得到9 6 0個相關值。因此 最後,關於最大值之該碼群與循環位置移動係分別被決定 為合理的碼群與碼框邊界。在步驟6 5 0中,第三階段處理 係判定該擾亂碼,藉由選擇一群中8個碼之一個,其中該 碼群已弟二階段被辨識。該第三階段處理判定可能的擾亂 碼’其中每隔2 5 6碼片就做一次判斷,並選取最大值戶斤相 對應的擾亂碼紀錄一次,最後,經過1 5 〇次紀錄後(一個碼 框長度),該最大得票數之值須作一第一驗證去決定該擾 亂碼是否正確。該最大得票數之值與一門欄值々^比較。 該門攔值7? G係根據固定錯誤警報率(c〇nstant false r a $ e )來決疋。在步驟6 6 0中,來自該第三階段處理 出係與一門攔值7? (ji乍比較,用以決定該擾亂碼是 。如果該門攔值未被超過,該試驗視為失敗,$ 一 在不延f下2重新開始。如果該門攔值被超過’該 ί ΐί ίΐ。在步驟670中’第二次驗證該擾 Γ 果該擾亂竭通過,則試驗係成 ί: ΐϊί:延遲時sΤρ毫秒(ms)後重新開 甚者,戎取樣點之選擇係仂e ^ 1Γ^ α / 辉保依序實現,且對每一個試 i /)Χ所此若整個細胞搜尋在第Κ次 成功,所而的細胞搜尋時間是(Κ+Ν+1)Χ 10毫秒567686 V. Description of the invention (14) The coherent accumulation is estimated by using the channel from the first stage. After collecting 15 secondary sibling codes, they are related to the 6 4 comma-free Reed Solomon code (CFRS) code word, each stone horse word has 1 5 possible cycles moving position. In this way, 960 correlation values are obtained. Therefore, in the end, the code group and the cyclic position movement system regarding the maximum value are determined as reasonable code group and code frame boundaries, respectively. In step 650, the third stage of processing is to determine the scrambling code by selecting one of eight codes in a group, where the code group has been identified in the second stage. The third stage of processing determines the possible scrambling codes. Among them, a judgment is made every 256 chips, and the scrambling code corresponding to the maximum household weight is selected to be recorded. Finally, after 150 times of recording (one code) Box length), the value of the maximum number of votes must be subjected to a first verification to determine whether the scrambling code is correct. The value of the maximum number of votes is compared with a gate value 々 ^. The threshold value of 7? G is determined based on a fixed false alarm rate (connstant false r a $ e). In step 6 60, the processing result from the third stage is compared with a threshold value of 7? (Ji is compared to determine the scrambling code. If the threshold value is not exceeded, the test is considered a failure, $ One restarts without delaying f. If the threshold value of the gate is exceeded, 'the ί ΐί ίΐ. In step 670, verify the disturbance a second time. If the disturbance passes, the test becomes ί: ίί: delay When sτρ is reopened after milliseconds (ms), the selection of sampling points is 仂 e ^ 1Γ ^ α / Huibao is realized in order, and for each trial i /) × if the entire cell is searched at the Kth time Success, and the cell search time is (Κ + Ν + 1) × 10 milliseconds

Harm 之該輸 否正破 新試驗 擾亂碼 亂碼是 功,否 始。更 驗需要 試驗才Harm's Loss Is Breaking New Test Scrambling Code Is the work a success, no. Correction requires experimentation

$ 19頁 567686 五、發明說明(15)$ 19 pages 567686 V. Description of the invention (15)

Cms ) ° 現請參考第七圖,該圖係 一種細胞搜尋方法,該方法 該每試驗隨機取樣方法之主 試驗接著一個試驗的基礎上 係在存在的取樣點中隨機的 下能有良好的助益。如第七 階段處理的過程,其各階段 解釋。如第七圖所示,其中 通道(PSCH)係用於時槽同步 通道(S S C Η)係在時槽同步後 階段73 0具有共同引導通道 決定。 顯示根據本發明第二實施例之 係使用每試驗隨機取樣方法。 要觀念係Ν個取樣點係在一個 隨機地被選擇去檢測。其動機 使用係在取樣頻率偏移的出現 圖所示,該方法中亦處理三個 處理之特徵係近似於第五圖的 苐一階段7 1 0具有一初級同步 。第二階段7 2 0具有次級同步 ’用於碼框/碼群辨識。第三 (CPICH)係用於下傳擾亂碼之 第八圖係顯示根據本發明之第二實施例之一種細胞搜尋 方法之流程圖,該方法係使用每試驗隨機取樣方法方法。 現請參照第八圖。在步驟8 0 0中,檢測來自基地台揮^進 入信號。在步驟810中,將該進入信號以碼片速率^^樣ν 次,且該過取樣後信號表示成γ 乂 k), γ 2( k )、、、 Υν(1〇。在步驟815中,將該進入信號降取樣且輪出該N個 過取樣點至N條平行信號路徑。在步騍8 2 0中,在該N過取 樣點中隨機地選取一取樣點並且傳送該N過取樣點中被選 取之一取樣點進行第一階段處理,第二階段處理與第三階 段處理。需注意的係,該檢測係在一個試驗接著一個試驗 的基礎上,每一個取樣點用於一個試驗。若配合第7圖更Cms) ° Please refer to the seventh chart, which is a cell search method. This method is based on the main test of the random sampling method for each test and the next test. It can help the random sampling in the existing sampling points. beneficial. As in the seventh stage of the process, its stages are explained. As shown in the seventh figure, the channel (PSCH) is used for time slot synchronization. The channel (S SC Η) is determined after the time slot synchronization. It is shown that a random sampling method per trial is used according to the second embodiment of the present invention. The idea is that N sampling points are randomly selected for detection. The motive use is shown in the appearance of the sampling frequency offset. The method also handles the three processing features which are similar to the first stage 7 1 0 of the fifth figure with a primary synchronization. The second stage 7 2 0 has secondary synchronization 'for code frame / code group identification. The third (CPICH) is the eighth figure for downloading the scrambling code. The eighth figure is a flowchart showing a cell search method according to the second embodiment of the present invention. The method uses a random sampling method per trial. Please refer to the eighth figure. In step 800, an incoming signal from the base station is detected. In step 810, the incoming signal is sampled ^ times at a chip rate, and the oversampled signal is represented as γ 乂 k), γ 2 (k),, Υν (1〇. In step 815, Down-sample the incoming signal and rotate the N oversampling points to N parallel signal paths. In step 8 2 0, randomly select a sampling point among the N oversampling points and transmit the N oversampling point. One of the sampling points was selected for the first stage treatment, the second stage treatment and the third stage treatment. It should be noted that the detection system is based on one test after another, and each sampling point is used for one test. If matched with Figure 7

567686 五、發明說明(16) 可清楚解釋第二實施例之該細胞搜尋方法係如何工作。 例來說,在第一次試驗中,在第一階段之方框7丨丨, 牛 階段之方框721與第三階段之方框73丨係測試相同的取樣一 點’其中該取樣點係隨機地選取以減低取樣頻沾 應。-旦該試驗錯誤,下一個新試驗將再次以 的取樣點。舉例來說,在第二次試驗中,在第一階$之 框712,第二階段之方框72 2與第三階段之方框73^X將 試相同選擇的取樣點,其中該取樣點係隨機地選取。如此 的試驗將一直進行,直到擾亂碼被該同步驗證過程所接 ,。更甚者’該取樣點之選擇係依序實現,如同傳統的導 管式搜尋方式,因此若整個細胞搜尋在第K次試驗才成 功,所需的細胞搜尋時間是(K + 2) X 10毫秒(ms)。 在步驟8 3 0中,第一階段處理得到第一階段之時槽同 步。一非同調的(non-coherent)匹配濾波器,其中該匹配 慮波器係分為複數個區段,且每一區段之輸出係以其絕對 值合併,係被分成四個區塊且作為一被使用在第一 中 作為時槽同步之一檢測器。非同調的累積超過丨5時;^被 適當地發現為白色高斯雜訊(additive white Gaussian noise)。為了較佳的特性,第一階段中超過一個時槽的 界被選擇進入下一個階段。 ,步驟8 4 0中,在時槽同步後,該碼群與碼框同步可以 在第二階段處理中完成。該第二階段處理,使用丨6個匹配 濾波為去檢測該次級同步碼。在第二階段之該同調的累積 (the coherent accumulati〇n)係可能的藉由使用來自第、567686 V. Description of the invention (16) It can clearly explain how the cell search method of the second embodiment works. For example, in the first test, in box 7 in the first stage, box 721 in the bull stage and box 73 in the third stage test the same sampling point, where the sampling point is random Select to reduce sampling frequency. -Once the test is wrong, the next new test will take the sampling point again. For example, in the second experiment, in the first stage of box 712, the second stage of box 72 2 and the third stage of box 73 ^ X will try the same selected sampling point, where the sampling point Selected randomly. Such tests will continue until the scrambling code is received by the synchronization verification process. What's more, the selection of the sampling points is realized sequentially, like the traditional catheter search method, so if the whole cell search is successful in the Kth test, the required cell search time is (K + 2) X 10 milliseconds (Ms). In step 830, the first-stage processing is synchronized with the first-time slot. A non-coherent matched filter, where the matched filter is divided into a plurality of sections, and the output of each section is combined with its absolute value, divided into four blocks and used as One is used in the first as a detector of time slot synchronization. When the non-homogeneous accumulation exceeds 5; ^ is appropriately found as additive white Gaussian noise. For better characteristics, the boundary of more than one time slot in the first stage is selected to enter the next stage. In step 8 40, after the time slot synchronization, the code group and code frame synchronization can be completed in the second stage of processing. In the second stage of processing, 6 matched filters are used to detect the secondary synchronization code. The coherent accumulative accumulation in the second phase (the coherent accumulati

567686 五、發明說明(17) 一階I又之該通道估計。在集合了 1 5個次級同步碼後,它們 係相關於5亥6 4無間斷里德-戶斤羅門瑪(c〇fflma — free Ree(j567686 V. Description of the invention (17) The first order I is the channel estimation. After the collection of 15 secondary synchronization codes, they are related to 5 Hai 64 4 uninterrupted Reed-Hujin Romainma (c〇fflma — free Ree (j

Solomon code,CFRS)碼字,每一碼字有15可能的循環移 動位置。如此得到9 6 0個相關值。因此最後,關於最大值 之該碼群與循環位置移動係分別被決定為合理的碼群與碼 框邊界。在步驟8 5 0中,第三階段處理係判定該擾亂碼, 藉由選擇一群中8個碼之一個,其中該碼群已第二階段被 辨識。該第三階段處理判定可能的擾亂碼,其中每隔256 碼片就做一次判斷,並選取最大值所相對應的擾亂碼紀錄 一次,最後,經過1 5 0次紀錄後(一個碼框長度),該最大 ,票數之值須作一第一驗證去決定該擾亂碼是否正確。該 最大得票數之值與一門欄值77 G比較。該門欄值々D係根 據固定錯誤警報率(constant false alarm rate)來決 疋。在步驟8 6 0中,來自該第三階段處理之該輸出係與一 門攔值。作比較,用以決定該擾亂碼是否正確。如果該 門攔值未被超過,該試驗視為失敗,且一新試驗在不延遲 下將重新開始。如果該門欄值被超過,該擾亂碼即進_第 ^驗證。在步驟8 70中,第二次驗證該擾亂碼是否被鼻 受’其中如果該擾亂碼通過,則試驗係成功,否則一新試 驗在一延遲時間T p毫秒(ms)後重新開始。 現請參考第九圖,該圖係顯示根據本發明第三實施例之 種細胞搜尋方法,該方法係使用每碼框隨機取樣方法。 如第九圖所示,該方法中亦處理三個階段處理的過程,其 各階段處理之特徵係近似於第七圖的解釋。並且,該第三Solomon code (CFRS) code words, each of which has 15 possible cyclic shift positions. In this way, 960 correlation values are obtained. Therefore, in the end, the code group and the cyclic position movement system regarding the maximum value are determined as reasonable code group and code frame boundaries, respectively. In step 850, the third stage processing determines the scrambling code by selecting one of eight codes in a group, wherein the code group has been identified in the second stage. This third stage of processing determines the possible scrambling codes, in which a judgment is made every 256 chips, and the scrambling code corresponding to the maximum value is selected to be recorded once. Finally, after 150 times of recording (one code frame length) The value of the maximum number of votes must be first verified to determine whether the scrambling code is correct. The value of the maximum number of votes is compared with a gate value of 77 G. The gate value 々D is determined based on a constant false alarm rate. In step 860, the output from the third stage processing is associated with a threshold. Compare to determine whether the scrambling code is correct. If the threshold is not exceeded, the test is considered a failure and a new test will be restarted without delay. If the value of the gate is exceeded, the scramble code is verified. In step 8 70, it is verified for the second time whether the scrambled code is nascent '. If the scrambled code passes, the test is successful, otherwise a new test is restarted after a delay time T p milliseconds (ms). Please refer to the ninth figure, which shows a cell search method according to the third embodiment of the present invention, which uses a random sampling method per yard. As shown in the ninth figure, the method also deals with a three-stage process. The characteristics of each stage of the method are similar to the explanation in the seventh figure. And the third

第22頁 567686 五、發明說明(18) 實施例之該方法非常近似 例係皆採用隨機取樣策略 法不同。該第三實施例之 框的基礎上,而不是如第 著一個試驗的基礎上。也 而,第三實施例之方法係 使用隨機取樣之一取樣點 現請參照 胞搜 一種細 樣方法 立地選 樣點進 需注意 上,而 第三階 是說, 第三實 第一次 與第三 該取樣Y2(k)、 碼框的 驗錯誤 。在 取一 行第 的係 不失 段處 他們 施例 試驗 階段 點係 方式 ,下 第十圖,該圖 寻方法之流程 步驟1020中, 取樣點並且傳 一階段處理, ,該檢測係在 其公平性。在 理所測試之取 係隨機且獨立 之該細胞搜尋 中,第一階段 之方框931 (見 隨機地且獨立 YN(k)中選取 被選取以減低 一個新試驗將 於第二實施例之方法,兩種實施 二其主要差別在取樣點的選擇方 ^亥方法係在一個碼框接著一個碼 =f施例之該方法在一個試驗接 就是說,第二實施例之方法係每 ,—隨機取樣之一取樣點。然 母一試驗中的每一階段各自獨立 〇 係顯示根據本發明第三實施例之 ,該方法係使用每碼框隨機取 在f N個過取樣點中隨機地且獨 =邊N過取樣點中被選取之一取 7階段處理與第三階段處理。 =個碼框接著一個碼框的基礎 理,第二階段處τ理與 的。若配合第ί::不—就 方法係如何m可清楚解釋 之方框911,第作_购舉例來說,在 第九圖)係測試之方框921 地白n個過取樣,其中 >該取樣點係—tYi(k)’ 個碼框接菩, 取樣頻率偏移的效^。#一者二個 再次測試隨機iS〜 〜喊言# 释破取的取樣點。^ 也Page 22 567686 V. Description of the invention (18) The method of the embodiment is very similar. The examples all use random sampling strategies. The third embodiment is based on the frame, rather than the first test. Also, the method of the third embodiment uses one of the sampling points for random sampling. Please refer to Cell Search for a fine sampling method to select the sampling points on the spot. Note that the third order is Third, the sampling Y2 (k) and the code frame are incorrectly checked. At the first line of the line, they have implemented the point system of the test phase. The tenth figure below, the process of step 1020 of the method of the figure finding method, sampling points and transmitting them in one stage, the detection system is in its fairness. . In a random and independent cell search that is tested by reason, the first stage of box 931 (see Random and Independent YN (k) is selected to reduce a new test method in the second embodiment) The main difference between the two implementation methods is the selection of sampling points. The method is in a code frame followed by a code = f. The method of this example is tested in a test. That is, the method of the second embodiment is random. Sampling is one sampling point. However, each stage in the mother-in-one test is independent. It is shown that according to the third embodiment of the present invention, the method uses each code frame to randomly take f N oversampling points randomly and independently. = One of the edge N oversampling points is selected for 7-stage processing and third-stage processing. = The basic principle of a code frame followed by a code frame, and the second phase is processed. If cooperate with the first ί :: 不 — As to how the method is m can be clearly explained in block 911, the first _ purchase example, in the ninth figure) is the test of box 921 and n oversampling, where the sampling point is-tYi (k ) 'Code frames are connected, the effect of sampling frequency offset ^. # 一 者 二个 Test random iS ~~ 〜 言 言 # Release the sampling points. ^ Also

第23頁 567686 五、發明說明(19) 就是說,第二次試驗中,在第一階段之方框9 1 2,第二階 段之方框9 2 2與第三階段之方框9 3 2亦將測試相同選擇的取 樣點,其中該取樣點係隨機地選取。如此的試驗將一直進 行,直到擾亂碼被該同步驗證過程所接受。更甚者,該取 樣點之選擇係依序實現,如同傳統的導管式搜尋方式,因 此右整個細胞搜哥在弟K次试驗才成功,所需的細胞搜尋 時間是(K + 2 )x 1 0毫秒(m s )。 第十一圖係顯示根據本發明實施例之一種細胞搜尋架 構’邊架構係實現本發明在非理想取樣效應與取樣頻率偏 移之效應下之細胞搜尋方法。 、 一種細胞搜尋裝置2 0 0,用於分碼多工接取系統,更特 別係用於寬頻分碼多工接取系統,該裝置處理三個階段之 通道。一碼片匹配濾波器210,用以匹配來自基地台之一 進入信號190。一取樣元件220,遠紝私兮u 土 口各丄〇口 21。,用以將該進入信號190以—片匹配慮波器 出過取樣之N個取樣點(Yl(k),Y2, J速率過v取樣輸 取樣器23 0,連結於該取樣元件用以、Y:(k))。·!降 點至一第一階段檢測器240、出該臟過取 三階段檢測器26〇。該第一階段檢』又欢測益25〇及一第 樣器23〇,用於得到該進人信號2上0二連接於該降取 二階段檢測器2 5 0,連結至該降取時槽同步。該第 入信號190之一碼群與碼框同步。;=^30,用以得到該進 連結至該降取樣器2 3 0,用以決定=、二=段檢測器2 6 0 ’ 碼。一控制元件2 3 5,連結至該窜'^進入信號1 9 0之一擾亂 。亥弟—階段檢測器240、該第Page 23 567686 V. Description of the invention (19) That is to say, in the second test, the box 9 1 2 in the first stage, the box 9 2 2 in the second stage and the box 9 3 2 in the third stage The same selected sampling point will also be tested, where the sampling point is randomly selected. Such tests will continue until the scrambling code is accepted by the synchronization verification process. What's more, the selection of the sampling points is realized sequentially, just like the traditional catheter search method. Therefore, the right whole cell search brother succeeded in the K trials. The required cell search time is (K + 2) x 10 milliseconds (ms). The eleventh figure is a cell search architecture according to an embodiment of the present invention. The edge architecture implements the cell search method of the present invention under the effects of non-ideal sampling effects and sampling frequency offsets. A cell search device 2000 is used for the code division multiplexing access system, and more particularly it is used for the wideband code division multiplexing access system. This device handles the three-stage channels. A chip matched filter 210 is used to match an incoming signal 190 from one of the base stations. A sampling element 220 is provided for each of the soil ports 21 and 21 respectively. For oversampling the incoming signal 190 with N-sampling points (Yl (k), Y2, J rate over-sampling input sampler 23 0), connected to the sampling element, Y: (k)). ·! Drop to a first-stage detector 240 and take out the dirty three-stage detector 26. The first-stage inspection is performed again with a test result of 25 and a sampler 23, which is used to obtain the entry signal 2 and connect it to the second-stage detector 250, which is connected to the second-stage detector. Slot synchronization. One code group of the first signal 190 is synchronized with the code frame. ; = ^ 30, used to obtain the forward link to the down-sampler 2 3 0, used to determine the =, 2 = segment detector 2 6 0 ′ code. A control element 235 is connected to one of the channeling entry signals 190 to disturb. Haidi—stage detector 240, the first

567686 五、發明說明(20) 二階段檢測器2 5 0及該第三階段檢測器2 6 0,用以控制該N 個過取樣點在該第一階段檢測器240、該第二階段檢測器 2 5 0及该弟二階段檢測器2 6 0中作不同的使用;以及一認證 單元2 80,連結於該第三階段檢測器26 0,用於決定該試驗 是否成功。該認證單元2 8 0更包含一比較器2 7 〇,連結至該 第三階段檢測器2 6 0,用以測試輸出自該第三階段之該擾 亂碼與一門棚值Θ 〇2 7 1比較。一第一決定元件2 7 5,連接 至該比較器2 7 0 ’用以決定該擾亂碼是否正確。一同步驗 證單位2 9 0,連結至該第一決定元件275,用以驗證該擾亂 碼。一弟一決定元件2 9 5,連接至該同步驗證單位2 9 〇,用 以決定該擾亂碼是否接受。設計人員可根據非理想取樣效 應與取樣頻率偏移之效應之情況,而控制該控制元件到本 發明之不同實施例。 更進一步的電腦模擬係使用於探討本發明之實施例之細 胞搜尋方法與傳統方法之操作特性之比較。此處強調非理 想取樣效應與取樣頻率偏移之效應。所有的數值結$係依 據:過取樣點N= 2,最大的都普勒飄移(maximuin j)4Pier s h i f t)係1 8 5 _ 2赫兹(相當於用戶裝置以1 〇 〇 _ k m / h r的速度 移動),每一階段的檢測係1 〇毫秒(m s),τ p = 2 5 〇毫秒(m s ) 且7?。係以10_4之錯誤警報率(c〇nstan1; false alarm rate)來設定。此外,該實際通道之傳輸功率係如下表 示。首先,初級同步通道與次級同步通道具有相同之功 率’且§亥共同引導通道與同步通道(初級同步通道+次級同 步通道)之功率比值係固定的。第二,該共同引導通道之567686 V. Description of the invention (20) The two-stage detector 250 and the third-stage detector 260 are used to control the N oversampling points in the first-stage detector 240 and the second-stage detector 250 and the second-stage detector 260 are used differently; and an authentication unit 2 80 is connected to the third-stage detector 260 to determine whether the test is successful. The authentication unit 2 80 further includes a comparator 2 7 0, which is connected to the third stage detector 2 60 to test the scrambling code output from the third stage and compare it with a door value Θ 0 2 71 . A first decision element 2 7 5 is connected to the comparator 2 7 0 ′ to determine whether the scrambling code is correct. A synchronous verification unit 290 is connected to the first decision element 275 to verify the scrambling code. A younger one decides the element 2 95 and is connected to the synchronous verification unit 2 90 to determine whether the scrambling code is accepted. The designer can control the control element to different embodiments of the present invention based on the effect of the non-ideal sampling effect and the effect of the sampling frequency offset. A further computer simulation is used to compare the operating characteristics of the cell search method of the embodiment of the present invention with the conventional method. The effects of undesired sampling and sampling frequency offset are emphasized here. All numerical values are based on: the oversampling point N = 2, the maximum is 4uier shift (maximuin j) 4 1ier (1 8 5 _ 2 Hz (equivalent to the user device at a speed of 100_ km / hr Movement), each stage of the detection system is 10 milliseconds (ms), τ p = 25 milliseconds (ms) and 7 ?. It is set with a 10_4 false alarm rate (connstan1; false alarm rate). In addition, the transmission power of the actual channel is shown below. First, the primary synchronization channel and the secondary synchronization channel have the same power ’, and the power ratio of the common channel and the synchronization channel (primary synchronization channel + secondary synchronization channel) is fixed. Second, of this common guiding channel

第25頁 567686Page 567686

f:發明說明(21) 中,恭為總傳輸功率之1 〇 %。換句話說,在細胞搜尋過程 I I基地台總傳輸功率之80%係貢獻在細胞内干擾。最 )系 幾何因子(geometry factor) G=(P i+Ppsc+Pssc+PpJ/p 值吏用於模組化該用戶裝置在細胞中之位置。愈高的 ^ ’表示該用戶裝置愈靠近該基地台附近。搜尋時間的蓄 貝的分布函數(CDF )係用來探討不同搜尋方法之特性指 fe 。 現請參考第十二圖,該圖係顯示根據本發明,在頻率偏 移所造成之取樣頻率偏移效應下之一種信號模型。該接收 到之L號r (t)使用一基頻(base-band )表示並給定為·· ’、中 Ppsc, Cpsc, Pssc,Cssc and Ppc,Cpc 係分別為該初級同 步通道,該次級同步通道與該共同引導通道之功率與展 碼。g(t)係表示雷利衰落(Rayleigh fading)增益其為 複數形式,h(t)係一上升餘弦函數之平方根(square r〇〇t raised cosine shaping function)並具有一繞屈因子 (roll - 0ff fact〇r)為0.22。 厶係該用戶裝置之碼片期 間。τ係初始隨機延遲且係以一隨機變數來模組,該變數 具有在整個(-0.5Tc, 〇_5Tc)之間均勻地分布。τ择該基 地台之碼片期間,且 Λ係該基地台之載波頻率,_係基f: In the description of the invention (21), Christine is 10% of the total transmission power. In other words, 80% of the total transmission power of the base station during the cell search process contributes to intracellular interference. The most) is the geometry factor G = (P i + Ppsc + Pssc + PpJ / p value is used to modularize the position of the user device in the cell. A higher ^ 'indicates that the user device is closer to the user device. Near the base station. The CDF of search time is used to explore the characteristic of different search methods, which is fe. Please refer to the twelfth figure, which shows the frequency shift caused by the frequency shift according to the present invention. A signal model under the effect of sampling frequency offset. The received L number r (t) is expressed using a base-band and given as ... ', Ppsc, Cpsc, Pssc, Cssc and Ppc, Cpc is the power and spreading code of the primary synchronization channel, the secondary synchronization channel and the common guidance channel. G (t) represents the Rayleigh fading gain, which is a complex form, h (t) is a The square root of the raised cosine function (square r〇t raised cosine shaping function) has a roll-off factor (roll-0ff fact0r) of 0.22. 厶 is the chip period of the user device. Τ is the initial random delay and is Module with a random variable, the variable has the integer (-0.5Tc, 〇_5Tc) are evenly distributed. Τ selects the chip period of the base station, and Λ is the carrier frequency of the base station,

第26頁 567686 五、發明說明(22) 地台與用戶裝置之間的頻率偏移量,f = /a /龙。此外, P!與Ρχ係分別為細胞内干擾(intra —ceU interferenc η i( t)與細胞間干擾(inter_ceii interference)nx(t)之功 率,其中…⑴與nx⑴係以白色高斯雜訊(additive white Gaussian noise)其統計平均值為零,且變異數為一之隨e 機程序(random processes )作為細胞内與細胞間干擾之才# 型。上述模型有三個觀察係值得在此提出。首先,為了 ^ 化,只考慮平坦的衰落通道(f lat fading),且只有有9 於該細胞搜尋之通道才被特別表示在我們的接收訊號表示 式;=有其他的通道係被包含在干擾項n1(t)或nx(t)之内、 了。第二,f係表示為取樣頻率偏移之效應,r係表示 非理想取樣效應,這些都是先前技術所忽略的。第三,= 模型中頻率偏移與非理想取樣效應係來自於傳播延遲〜 (propagation del ay)不確定以及頻率偏移所造成的相位 偏,及取樣頻率偏移來自相同的震盪器來源。 第十二圖係顯示在有非理想取樣效應且取樣頻率偏 應 f:0kHz下,比較不同細胞搜尋方法之特性圖。其中\ 理想係用來表示理想取樣。如圖所示,非理想取樣造 嚴重的操作特性破壞,特別係在較低的信號雜訊比 (signal to n〇ise ratio ’ SNR)的案例中(一較小的增只 值)。在此圖中,對所有的搜尋策略及信號雜訊比增^ ^ 6dB時,90%的機會(occasi〇ns)會在11〇毫秒内被完成。另 方面在彳&號雜訊比增盈G為〇 d B時,根據本發明之第一Page 26 567686 V. Description of the invention (22) The frequency offset between the platform and the user equipment, f = / a / dragon. In addition, P! And Pχ are the power of intra-ceU interferenc η i (t) and inter_ceii interference nx (t) respectively, where ⑴ and nx⑴ are white Gaussian noise (additive) white Gaussian noise) whose statistical average is zero, and the number of variations is one. Random processes are used as the type of intra- and inter-cell interference. The above model has three observation systems that are worthy of being proposed here. First, For the sake of simplicity, only flat fading channels (f lat fading) are considered, and only 9 channels searched by the cell are specifically expressed in our received signal expression; = other channels are included in the interference term n1 (t) or nx (t). Second, f is the effect of sampling frequency offset, and r is the effect of non-ideal sampling, which are ignored by the prior art. Third, = in the model The frequency offset and non-ideal sampling effects come from the propagation delay ~ (propagation del ay) uncertainty and the phase offset caused by the frequency offset, and the sampling frequency offset comes from the same oscillator source. Under the non-ideal sampling effect and the sampling frequency response f: 0kHz, compare the characteristics of different cell search methods. Among them, \ ideal is used to represent ideal sampling. As shown in the figure, non-ideal sampling causes serious damage to operating characteristics. Especially in the case of lower signal to noise ratio (SNR) (a small increase only). In this figure, all search strategies and signal to noise ratio increase ^ ^ At 6dB, a 90% chance (occasion) will be completed in 11 milliseconds. On the other hand, when the noise and gain ratio 彳 &

567686 五、發明說明(23) 實施例之細胞搜尋方法(STS1 )能在3 0 0毫秒内完成90%的搜 尋率,但是對傳統搜尋策略卻花了 4 5 0毫秒(m s ),對本發 明之第二實施例之細胞搜尋方法(RSPT)卻花了 38 0毫秒 (ms),對本發明之第三實施例之細胞搜尋方法(rspf)卻花 了超過6 0 0毫秒(ms)。 第十四圖係顯示在有非理想取樣效應且取樣頻率偏移效 應 A = 8 Κ Η z下,比較不同細胞搜尋方法之特性圖。在此狀 況下,在一試驗期間,取樣頻率偏移幾乎達到碼片時間一 半。如果在第三階段之末端,取樣頻率偏移大過一碼片時 間,則該一個試驗將永遠不成功。如圖所示,本發明之第 二實施例之細胞搜尋方法(RSPT)與本發明之第三實施例之 細胞搜尋方法(RSPF )比起傳統方法有重要改善。此係由於 取樣頻率偏移的出現下,隨機取樣在三個階段中具有較佳 的機會去得到更合理的取樣點。 第十五圖係顯示在有非理想取樣效應且取樣頻率偏移 應= 1 2ΚΗζ下,比較不同細胞搜尋方法之特性圖。隨丨 取樣頻率偏移的增大,傳統方式與本發明之第一實施例之 細胞搜尋方法(STS1 )、本發明之第二實施例之細胞搜尋方 法(RSPT)及本發明之第三實施例之細胞搜尋方法(RSpF)i 操作特性之差異變得愈大。由第丨4圖與第丨5圖知,在取樣 頻率偏移狀況下時,本發明之第三實施例之細胞搜尋方法 (R S P F )係較佳的選擇。 因此’根據本發明用於分碼多工接取系統之該細胞搜尋567686 V. Description of the Invention (23) The cell search method (STS1) of the embodiment can complete a search rate of 90% in 300 milliseconds, but it takes 450 milliseconds (ms) to the traditional search strategy. The cell search method (RSPT) of the second embodiment took 380 milliseconds (ms), and the cell search method (rspf) of the third embodiment of the present invention took more than 600 milliseconds (ms). The fourteenth graph is a comparison of the characteristics of different cell search methods under the non-ideal sampling effect and the sampling frequency offset effect A = 8 K Η z. In this case, during a test, the sampling frequency shift was almost half the chip time. If at the end of the third phase, the sampling frequency is shifted by more than one chip time, the test will never succeed. As shown in the figure, the cell search method (RSPT) of the second embodiment of the present invention and the cell search method (RSPF) of the third embodiment of the present invention have an important improvement over the conventional method. Due to the occurrence of sampling frequency offset, random sampling has a better chance to obtain more reasonable sampling points in three stages. The fifteenth figure shows the comparison of the characteristics of different cell search methods under the non-ideal sampling effect and the sampling frequency offset should be 1 2KΗζ. With the increase in the sampling frequency offset, the traditional method and the cell search method (STS1) of the first embodiment of the invention, the cell search method (RSPT) of the second embodiment of the invention, and the third embodiment of the invention The greater the difference in the operating characteristics of the cell search method (RSpF) i. It is known from FIG. 4 and FIG. 5 that the cell search method (RSP F) of the third embodiment of the present invention is a better choice when the sampling frequency is offset. Therefore, the cell search for a code division multiplexing access system according to the present invention

第28頁 567686 五、發明說明(24) 方法’月皂在此分碼多丁接 成之效應及快速達到初始同步。 ^ 所造 处,據本發明用於分碼多工接取系統之該細胞搜尋裴置 月匕在頻率偏移所造成之取樣頻率偏移效應實現細胞搜尋裝 置且不增加硬體的複雜度。咸信,根據本發明之方法與裝 置係可用於行動裝置與無線個人數位化助理(PDA)系統。 f 本發明已以前述較佳施例示,然並非用以限 r ^ 任何熟習此技藝者,在不脫離本發明之精神和Page 28 567686 V. Explanation of the invention (24) Method ‘The effect of the moon soap on the code division and the fast synchronization of the initial synchronization. ^ According to the invention, according to the present invention, the cell searcher Pei Zhiyue used in the code division multiplexing access system achieves the cell frequency search effect without increasing the complexity of the hardware. It is believed that the method and device according to the present invention are applicable to mobile devices and wireless personal digital assistant (PDA) systems. f The present invention has been illustrated with the foregoing preferred embodiments, but it is not intended to limit r ^ Any person skilled in the art will not depart from the spirit and scope of the present invention.

摩巳圍内,去7仏A 田』作各種之更動與修改。因此本發明之保護範 欠r仃之申请專利範圍所界定者為準。Inside Capricorn, go to 7 仏 A and make various changes and modifications. Therefore, the protection scope of the present invention shall be defined by the scope of patent application.

567686 圖式簡單說明 【圖表簡單說明】 表一顯示在不同頻率偏移的狀況下所產生的取樣頻率偏 移。 7 第一圖係顯示一用於第三代合作計晝之寬頻八滿多少换 取/分頻多工系統之簡化碼框結構圖。 第二(a )圖係顯示一用於第三代合作計畫之寬 分痛多 工接取/分頻多工系統之傳統的依序式細胞搜尋方、法。(在 此例中,每一階段之過程時間係設為為丨〇毫秒 ))。 苐^一( b)圖係顯不一用於第三代合作計書之寬分痛^ 工接取/分頻多工系統之傳統的導管式細胞搜尋方、法。(在 此例中,每一階段之過程時間係設為為丨〇毫秒(^ s ))。 第三(a)圖與第三(b)圖顯示,由於頻率偏移所成之取 樣頻率偏移效應下,信號位準降低與碼片間干^二如的結 果。 ’ 第四圖係顯示使用本發明之一種細胞搜尋方法之控制過 程。 ‘免募 第五圖係顯示根據本發明第一實施例之一種細胞搜尋11¾ 法,該方法係使用第一階段依序測試(s e r i a 1 t e s t i η stage-1, STSI)方法。 第六圖係顯示根據本發明第一實施例之一種細胞搜尋方 法之流程圖,該方法係使用第一階段依序測試方法。 第七圖係顯示根據本發明第二實施例之一種細胞搜尋方 法’該方法係使用每試驗隨機取樣(r a n d 〇 m s a m ρ 1 i n g p e r tria 卜 RSPT)方法。567686 Simple description of the diagram [Simplified description of the diagram] Table 1 shows the sampling frequency offset generated under different frequency offset conditions. 7 The first picture is a simplified code frame structure diagram of the third-generation cooperative calculation of the day-to-day broadband / reach / division multiplexing system. The second (a) diagram shows a traditional sequential cell search method and method for the wide-spread multi-multiplexed access / frequency-division multiplexed system used in the third-generation cooperative project. (In this example, the process time of each stage is set to 丨 0 milliseconds).苐 ^ 1 (b) The picture shows the traditional wide-spreading method used in the third-generation cooperative book ^ industrial access / frequency division multiplexing system. (In this example, the process time of each stage is set to 〇0 milliseconds (^ s)). Figures 3 (a) and 3 (b) show the results of the reduction in signal level due to the effect of sampling frequency offset caused by the frequency offset and the chip-to-chip interference. The fourth diagram shows a control process using a cell searching method of the present invention. ‘No recruitment. The fifth diagram is a cell search method according to the first embodiment of the present invention, which uses the first stage sequential test (serial a stage 1 t e s t n n stage-1, STSI) method. The sixth diagram is a flowchart of a cell search method according to the first embodiment of the present invention. The method uses a first-stage sequential testing method. The seventh figure shows a cell search method according to the second embodiment of the present invention. This method uses a random sampling (r a n d 0 m s a m ρ 1 i n g p r r tria (RSPT)) method per test.

第30頁 567686 圖式簡單說明 第八圖係顯示根據本發明第二實施例之一種細胞搜尋方 法之流程圖,該方法係使用每試驗隨機取樣方法。 第九圖係顯示根據本發明實施例第三之一種細胞搜尋方 法’該方法係使用每碼框隨機取樣(r a n d 〇 m s a m p 1 i n g p e r frame ’ RSPF )方法。 第十圖係顯示根據本發明實施例第三之一種細胞搜尋方 法之流程圖,該方法係使用每碼框隨機取樣方法。 第Η 圖係顯示根據本發明實施例之一種細胞搜尋架 構丄該架構係實現本發明之細胞搜尋方法。 ,十^圖係顯示根據本發明之一種信號模型。 第十三圖係顯示在有非理想取樣效應且取樣頻率偏移效 應—Λ =0kHz下,比較不同細胞搜尋方法之特性圖。 第十四圖係顯示在有非理想取樣效應且取樣頻率偏移效 應Λ = 8 k Η z下,比較不同細胞搜尋方法之特性圖。 , 第十五圖係顯示在有非理想取樣效應且取樣頻率偏移 應Λ - 1 2 k Η z下,比較不同細胞搜尋方法之特性圖。 【圖號說明】 111 初級同步通道 121 次級同步通道 131 共同引導通道 190 號 200 細胞搜尋裝置 210 碼片匹配濾波器 220 取樣元件 230 降取樣器 235 控制元件Page 567686 Brief Description of Drawings Figure 8 is a flowchart showing a cell search method according to the second embodiment of the present invention, which uses a random sampling method per test. The ninth figure shows a third cell search method according to an embodiment of the present invention. The method uses a random sampling per code frame (r n d 0 m s a m p 1 i n g p r r frame ′ RSPF) method. The tenth figure is a flowchart of a cell search method according to the third embodiment of the present invention. The method uses a random sampling method per frame. Figure IX shows a cell search architecture according to an embodiment of the present invention. This architecture implements the cell search method of the present invention. Figure 10 shows a signal model according to the present invention. The thirteenth figure is a comparison of the characteristics of different cell search methods in the presence of non-ideal sampling effects and sampling frequency offset effects-Λ = 0 kHz. The fourteenth graph is a comparison of the characteristics of different cell search methods with non-ideal sampling effects and sampling frequency offset effects Λ = 8 k Η z. The fifteenth figure shows the comparison of the characteristics of different cell search methods under the non-ideal sampling effect and the sampling frequency offset should be Λ-1 2 k Η z. [Illustration of figure number] 111 primary synchronization channel 121 secondary synchronization channel 131 common guidance channel 190 200 cell search device 210 chip matching filter 220 sampling element 230 down sampler 235 control element

567686 圖式簡單說明 240 第 - 階 段 檢 測 器 250 第 二 階段 檢 測器 260 第 三 階 段 檢 測 器 270 比 較 器 271 門 欄 值 V 0 275 第 一 決 定 元 件 280 認 證 單 元 290 同 步 驗證 單 元 295 第 二 決 定 元 件 liiil 第32頁567686 Schematic description 240 First-stage detector 250 Second-stage detector 260 Third-stage detector 270 Comparator 271 Gate value V 0 275 First decision element 280 Authentication unit 290 Synchronization verification unit 295 Second decision element liiil Page 32

Claims (1)

567686 年Λ 04」充 一案號91臟7fi 六、申請專利範圍 1 · 一種細胞搜尋方法,用%八作々 t ^ 於刀碼多工接取系統,該方法中 使用三個階段之細胞搜尋 # 士 4 a人 T ^仅+過私,該方法包含下列步驟: 匹配(matc>h)來自基地台之一進入信號; # it ^ ^ m ^ ^ ^ # ϋ ¢1 #ν ^ ϋ ¢, ^ 個取樣點(Y“k),Y2(k)、、、Y“k)); 取樣之w 將孩進入#旎降取樣且輸出該N個取樣點至 路徑; τ 1丁 Ί口贶 將該N個過取樣點依序作一第一階段處理,一第二 處理及二第三階段處理以完成一個試驗(triai) ,· 其中藉由一控制過程,該N個過取樣點在該第一階段處 理,該第二階段處理及該第三階段處理中係有不同的使 用。 2夺依申請專利範圍第丨項之細胞搜尋方法,其中該細胞搜 哥之該試驗更包含下列步驟·· 在第一階段處理中,可得到該進入信號之一時槽同步,· 在第二階段處理中,檢測該進入信號之一碼群與碼框同 步; 在第三階段處理中,選擇該進入信號之一擾亂碼; 測試該擾亂碼與一門攔值^^作一第一認證; 其中如果該門欄值未被超過,則該試驗視為失敗,且一 新試驗在不延遲下將重新開始;否則 所選之該擾亂碼進行一第二驗證; 其中如果該擾亂碼通過該第二驗證,則試驗係成功,否567 04 in 567686 ", with a case number of 91 dirty 7fi 6. Application scope 1. A cell search method, which uses %% as the 々t ^ in the knife-code multiplexing access system, which uses three stages of cell search # 士 4 a person T ^ only + private, this method includes the following steps: match (matc > h) the incoming signal from one of the base stations; # it ^ ^ m ^ ^ ^ # ϋ ¢ 1 # ν ^ ϋ ¢, ^ Sampling points (Y "k), Y2 (k) ,,, Y" k)); sampling w will enter # 旎 down sampling and output the N sampling points to the path; τ 1 丁 Ί 口 贶 will The N oversampling points are sequentially processed in a first stage, a second process, and a second and third stage to complete a trial (triai), where by a control process, the N oversampling points are in the first stage There are different uses in the one-stage process, the second-stage process, and the third-stage process. 2 According to the method of cell search according to the scope of the patent application, the test of the cell search brother further includes the following steps: · In the first stage of processing, one of the access signals can be synchronized with the time slot. · In the second stage In the process, it is detected that one code group of the incoming signal is synchronized with the code frame. In the third stage of processing, a scramble code of the incoming signal is selected; the scramble code and a threshold value ^^ are tested as a first authentication; If the gate value is not exceeded, the test is deemed to have failed, and a new test will be restarted without delay; otherwise, the scrambled code is selected for a second verification; wherein if the scrambled code passes the second verification , The test was successful, no 第33頁 567686 案號 91107676 修正 松10.31修正年Λ B说备 補凡 六、申請專利範圍 則一新試驗 間TP毫秒(ins)後重新開始 3. 依申請專利範圍第1項之細胞搜尋方法’其中該控制過 程更包含下列步驟: 在第一階段處理中,在該N個過取樣點中選取一最佳取 樣點。 4. 依申請專利範圍第3項之細胞搜尋方法,其中該N過取樣 點中之該最佳取樣點在沒有干擾出現下,係在該N過取樣 點中具有最大的取樣值。 5.依申請專利範圍第1項之細胞搜尋方法,其中該控制過 程更包含下列步驟: 在第一階段處理中,在該N個過取樣點中隨機地選取一 取樣點,並傳送至第二階段處理及第三階段處理,以進行 在該試驗的三階段處理。 6 ·依申請專利範圍第1項之細胞搜尋方法,其中該控制過 程更包含下列步驟: 左在第一階段處理、第二階段處理及第三階段處理時,係 •^機且獨立地在該N個過取樣點中選取一取樣點,以在該 試驗的每一階段中處理。 7 ·依申請專利範圍第2項之細胞搜尋方法,其中該第一階Page 33 567686 Case No. 91107676 Amendment Pine 10.31 Amendment Year Λ B said to be supplemented Sixth, the scope of the patent application is a new test room TP milliseconds (ins) restarted 3. According to the cell search method of the first scope of the patent application The control process further includes the following steps: In the first-stage processing, an optimal sampling point is selected from the N oversampling points. 4. The cell search method according to item 3 of the scope of patent application, wherein the best sampling point in the N oversampling point has the largest sampling value in the N oversampling point without interference. 5. The cell searching method according to item 1 of the patent application scope, wherein the control process further includes the following steps: In the first stage of processing, a sampling point is randomly selected from the N oversampling points and transmitted to the second The stage treatment and the third stage treatment were performed in the three stages of the test. 6. The cell search method according to item 1 of the scope of patent application, wherein the control process further includes the following steps: When the first stage processing, the second stage processing and the third stage processing are performed, the system is independently A sampling point is selected from the N oversampling points to be processed at each stage of the test. 7 · Cell search method according to item 2 of the patent application scope, wherein the first stage 第34頁Page 34 段處理更包含下列步驟: 在一初級同步通道中,係使用一般化階級制的葛雷序列 (generalized hierarchical Go 1 ay sequence)作為一初 級同步碼。 8 ·依申請專利範圍第2項之細胞搜尋方法,其中該第二階 段處理更包含下列步驟: 在一次級同步通道中,使用1 6個次級同步碼,其中該次 級同步碼係與該初級同步碼正交。 9 ·依申請專利範圍第8項之細胞搜尋方法,其中該次級同 步通道藉由使用一(15, 3)之無間斷里德-所羅門碼(c〇mma一 free Reed Solomon code,CFRS),更進一步被編碼成一 組64碼字,其中該組之每一碼字被表成一碼群,用以辨識 一碼框邊緣及碼群。 10·依申請專利範圍第2項之細胞搜尋方法,其中該第: 階段處理更包含下列步驟: 八 ^ 一 在該碼群被辨識後,該擾亂碼可以經由一共同引導通 道,選擇8個碼字中之一個來決定。 ^ 、 11·依申請專利範圍第7項之細胞搜尋方法,i 級同步碼中選擇超過-個以上之時槽邊界作為、—較佳^ 之候選者(candidate),雖然僅有一時槽邊界是正確的。Segment processing further includes the following steps: In a primary synchronization channel, a generalized hierarchical Go 1 ay sequence is used as a primary synchronization code. 8. The cell search method according to item 2 of the scope of patent application, wherein the second-stage processing further includes the following steps: In the primary synchronization channel, 16 secondary synchronization codes are used, wherein the secondary synchronization code is related to the The primary synchronization code is orthogonal. 9. The cell search method according to item 8 of the scope of the patent application, wherein the secondary synchronization channel uses a (15, 3) uninterrupted Reed-Solomon code (c0mma-free Reed Solomon code, CFRS), It is further encoded into a group of 64 codewords, where each codeword of the group is represented as a code group for identifying a code frame edge and a code group. 10. The cell search method according to item 2 of the scope of the patent application, wherein the stage: stage processing further includes the following steps: ^^ After the code group is identified, the scrambled code can pass a common guidance channel, and select 8 codes One of the words. ^, 11. According to the cell search method of the 7th scope of the patent application, i-level synchronization codes select more than one or more time slot boundaries as candidates for better ^, although only one time slot boundary is correct. 567686567686 1 z 依申請專利範圍第9 Jg 階段處理之該碼框邊界鱼、t之、:、、田胞搜尋方法,其中在第二 位置之最大值。 人I群係為該碼群與該循環的移動 13. 依申請專利範圍筮9 ϋ 7? ^ ^ ί±1 ^ 員之細胞搜尋方法,其中該門欄 值π 0係根據固定錯誤邀齟 u爛 rate)來決定。 a 報率(constant false alarm 1 4 · 依申請專利節if)楚1 tS1 z The method of searching for the border frame fish, t,:, and cell of the code frame according to the 9th Jg stage of the scope of the patent application, where the maximum value is at the second position. The human I group is the movement of the code group and the cycle 13. According to the scope of the patent application 筮 9 ϋ 7? ^ ^ ± 1 ^ members of the cell search method, where the gate value π 0 is invited according to a fixed error 龃 u Bad rate) to decide. a report rate (constant false alarm 1 4 · according to patent application if) Chu 1 tS 搜尋方法係使用於項之細胞搜尋方法,其中該細月 、 於見頻分碼多工接取/分頻雙工系統。 ^尋專利範圍第1工員之細胞搜尋方法,其中該細月 系統。/糸使用於行動裝置與無線個人數位化助理(PDA 一· 一種細胞搜尋裝置 實現三個階段之細胞搜 —碼片匹配濾波器, ,用於分碼多工接取系統,該裝置 尋,該細胞搜尋裝置包含: 用以匹配來自基地台之一進入信The search method is a cell search method used in the term, wherein the fine month is in a frequency division code multiplexed access / frequency division duplex system. ^ Cell search method for workers in patent scope No. 1 in which the fine month system. / 糸 Used in mobile devices and wireless personal digital assistants (PDA1. A cell search device to achieve three stages of cell search-chip matching filter, used for code division multiplexing access system, the device seeks, the The cell search device includes: to match an incoming letter from one of the base stations 位咕、羡元件’連結於該碼片匹配濾波器,用以將該進入 1 口 5泥以一石馬Η 、* + /1 X Λ 巧月迷率過取樣Ν次並輸出過取樣之Ν個取樣點(Yi ,:2(k)、、八⑴); 一降取;1¾奘 保為,連結於該取樣元件,用以輸出該N個過取The bit-gu, envy element 'is connected to the chip-matched filter, which is used to over-sample the input 1 mouth 5 mud with a stone horse, * + / 1 X Λ Qiaoyue fan rate N times and output N over-sampled Sampling points (Yi ,: 2 (k) ,, ⑴); one drop; 1¾ 奘 is connected to the sampling element to output the N overtakes 第36頁 567686 案號 91107B7R 年 月 日 六、申請專利範圍 修正Page 36 567686 Case No. 91107B7R 階段 檢測器 該第 入信號 該第 入信號 該第 點至一第一階段檢測器、一第二階段檢測器及一 檢測器; 接於該降取樣器,用於得到該進 結至該降取樣器,用以得到該進 步; 結至該降取樣器,用以決定該進 第一階段檢測器、該第二階段檢 ’用以控制該N個過取樣點在該 階段檢測器及該第三階段檢測器 第三階段檢測器,用於決定該試 一階段檢測器,連 之之一時槽同步; 一階段檢測器,連 之一碼群與碼框同 三階段檢測器,連 入信號之一擾亂碼; 一控制元件 測器及該第三 ’連結至該 階段檢測器 用;以及 ’連結於該 第一階段檢測器、該第二 中作不同的使 一認證單元 驗是否成功。 17·依申請專利範圍第1 6項之細胞搜尋裝置,其中該認證 單元更包含: 比車乂器’連結至該第三階段檢洌器,用以測試輸出自 该第三階段之該擾亂碼與一門攔值々。比較; 一第一決定元件,連接至該比較器,用以決定該擾亂碼 是否正確; 其中如果該門欄值未被超過,則該試驗視為失敗,且一 新試驗在不延遲下將重新開始,反之,如果該門攔值被超 過’則所決定之該擾亂碼即進入一同步驗證單元;The phase detector, the first input signal, the first input signal, the first point to a first phase detector, a second phase detector, and a detector; connected to the down sampler for obtaining the ingress to the down sampling Device to obtain the progress; to the down-sampler to determine the first-stage detector, the second-stage detector to control the N oversampling points in the stage detector and the third Phase detector The third-stage detector is used to determine the one-stage detector of the test, and one of the time slots is synchronized; the one-stage detector, and the code group and frame are the same as the three-stage detector, and one of the incoming signals A scramble code; a control element detector and the third 'connected to the stage detector; and' connected to the first stage detector and the second to make a verification unit successful. 17. The cell search device according to item 16 of the scope of the patent application, wherein the authentication unit further includes: than the car's device is connected to the third-stage detector to test the scramble code output from the third stage With a door blocking value. Compare; a first decision element connected to the comparator to determine whether the scrambling code is correct; wherein if the gate value is not exceeded, the test is considered a failure, and a new test will be repeated without delay Initially, on the contrary, if the threshold value is exceeded, the determined scrambling code enters a synchronization verification unit; 第37頁 567686 ------------------车月曰 六、申請專利範圍 修正 92·10·31 修 lL 年月日4 士補充 °亥同步驗證單位,連結至該第一決定元件,用以驗證該 擾IL碼;以及 <弟一決定元件,連接至該同步驗證單位,用以決定該 擾亂碼是否接受; 其中如果該擾亂碼通過該第二決定元件,則試驗係成 功’否則一新試驗在一延遲時間TP毫秒(ms )後重新開 始0 18·依申請專利範圍第丨6項之細胞搜尋裝置,其中該第一 階段檢測器藉由該控制元件之控制,在該N個過取樣點中 選取一最佳取樣點。 19. 依申請專利範圍第1 8項之細胞搜尋裝置,其中該最佳 取樣點在沒有干擾出現下,係在該N過取樣點中具有最大 的取樣值。 20. 依申請專利範圍第1 6項之細胞搜尋裝置,其中該第一 階段檢測器藉由該控制元件之控制,在該N個過取樣點中 隨機地選取一取樣點,並依序傳送至該第二階段檢測器及 該第三階段檢測器,以繼續進行該三階段之細胞搜尋。 21. 依申請專利範圍第1 6項之細胞搜尋裝置,其中藉由該 控制元件之控制,該第一階段檢測器、該第二階段檢測器 及該第三階段檢測器’係隨機且獨立地在該\個過取樣點567686 on page 37 ------------------ Car month date 6. Amendment of the scope of patent application 92 · 10 · 31 Rev. lL yyyyyyyyymmmm 4 shi added ° Hai synchronization verification unit, Connected to the first decision element for verifying the scrambled IL code; and < a first decision element connected to the synchronization verification unit for determining whether the scramble code is accepted; wherein if the scramble code passes the second decision Element, the test is successful. Otherwise, a new test restarts after a delay time of TP milliseconds (ms). The cell search device according to item 6 of the patent application scope, wherein the first stage detector is controlled by the For component control, an optimal sampling point is selected from the N oversampling points. 19. The cell searching device according to item 18 of the scope of patent application, wherein the optimal sampling point has the largest sampling value among the N oversampling points without interference. 20. The cell searching device according to item 16 of the scope of patent application, wherein the first-stage detector randomly selects one sampling point among the N oversampling points under the control of the control element, and sequentially transmits the sampling points to The second-stage detector and the third-stage detector to continue the three-stage cell search. 21. The cell search device according to item 16 of the scope of patent application, wherein the first-stage detector, the second-stage detector, and the third-stage detector are randomly and independently controlled by the control element. At the \ oversampling points 第38頁 567686Page 567686 ―案號 91107676 年月 日 修正 六、申請專利範圍 中選取一取樣點,以在各階段檢測器中處理。 22·依申請專利範圍第16項之細胞搜尋裝置,其中該第一 檢測器在一初級同步通道中,係使用一般化等級制度的葛 雷序列(generalized hierarchical Golay sequence)作 為一初級同步碼。 2 3·依申請專利範圍第1 6項之細胞搜尋裝置,其中該第二 檢測器在一次級同步通道中,係使用丨6個次級同步碼,其 中該次級同步碼係與該初級同步碼正交。 2 4·依申請專利範圍第2 3項之細胞搜尋裝置,其中該次級 同步通道藉由使用一(1 5,3)之無間斷里德—所羅門碼 (comma-free Reed Solomon code,CFRS),更進一步被編 碼成一組64碼字,其中該組之每一碼字被表成一碼群,用 以辨識一碼框邊緣及碼群。 2 5·依申睛專利範圍第1 6項之細胞搜尋裝置,其中在該碼 群被辨谶後’該擾亂碼可以經由一共同引導通道,選擇8 個碼字之一個來決定。 2 6·依申睛專利範圍第1 6項之細胞搜尋裝置,其中該第一 階段檢測器使用一非同調合成匹配濾波器執行時槽同步。―Case No. 91107676 Date Amendment 6. Select a sampling point in the scope of patent application for processing in the detector at each stage. 22. The cell search device according to item 16 of the application, wherein the first detector uses a generalized hierarchical Golay sequence as a primary synchronization code in a primary synchronization channel. 2 3. The cell search device according to item 16 of the scope of patent application, wherein the second detector uses a 6 secondary synchronization codes in a secondary synchronization channel, wherein the secondary synchronization codes are synchronized with the primary The codes are orthogonal. 24. The cell search device according to item 23 of the scope of patent application, wherein the secondary synchronization channel uses a (1, 5, 3) uninterrupted Reed-Solomon code (CFRS) Is further encoded into a group of 64 codewords, where each codeword of the group is represented as a code group to identify a code frame edge and code group. 25. The cell search device according to item 16 of Yishenyan's patent, wherein after the code group is identified, the scramble code can be determined by selecting one of 8 code words through a common guidance channel. 26. The cell search device according to item 16 of the Yishen patent, wherein the first-stage detector uses a non-homogeneous synthetic matched filter to perform time slot synchronization. ΖΊ 依甲請專利範圍第 567686 _殺於、目,1 口。+二 月包搜尋裝置,其中該弟 =^,測益在该初級同步碼中選擇超過一個以上之時槽邊 界作為一較佳操作之候€,雖然僅有一候選將被考慮到。 胞搜尋裝置,其中該第 以檢測該次級同步碼。 28·依申請專利範圍第23項之細 階段檢測器使用1 6個匹配濾波器 29·依申請專利範圍第24項之細胞搜尋裝置,其中該第二 階段檢測器檢測該碼群與該循環的以作 為該碼群與碼框邊界。 動位置之敢人 3 0·依申請專利範圍第1 7項之細胞搜尋裝置,其中該門攔 值7/ G係根據固定錯誤警報率來決定。 31.依申請專利範圍第1 7項之細胞搜尋裝置,其中該細胞 搜尋裝置係使用於寬頻分碼多工接取/分頻雙工系統。 3 2·依申請專利範圍第1 7項之細胞搜尋裝置,其中該細胞 搜尋裝置係使用於行動裝置與無線個人數位化助理PDA 系統。ZΊ According to the patent, please apply for the scope of patent No. 567686 _ kill Yu, head, 1 mouth. + February packet search device, where the brother = ^, test benefit selects more than one time slot boundary in the primary synchronization code as a better operation, although only one candidate will be considered. The cell search device, wherein the first detecting the secondary synchronization code. 28. The fine-phase detector according to item 23 of the patent application uses 16 matched filters. 29. The cell search device according to item 24 of the patent application, wherein the second-stage detector detects the code group and the loop. Let this be the boundary between the code group and the code frame. Dare man in moving position 30. According to the cell search device of the 17th scope of the patent application, the threshold value 7 / G is determined according to a fixed false alarm rate. 31. The cell searching device according to item 17 of the scope of patent application, wherein the cell searching device is used in a wideband division code multiplexed access / division duplex system. 32. The cell search device according to item 17 of the scope of patent application, wherein the cell search device is used in a mobile device and a wireless personal digital assistant PDA system.
TW91107676A 2002-04-12 2002-04-12 Method and apparatus for cell search for W-CDMA TW567686B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
TW91107676A TW567686B (en) 2002-04-12 2002-04-12 Method and apparatus for cell search for W-CDMA

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
TW91107676A TW567686B (en) 2002-04-12 2002-04-12 Method and apparatus for cell search for W-CDMA

Publications (1)

Publication Number Publication Date
TW567686B true TW567686B (en) 2003-12-21

Family

ID=32502544

Family Applications (1)

Application Number Title Priority Date Filing Date
TW91107676A TW567686B (en) 2002-04-12 2002-04-12 Method and apparatus for cell search for W-CDMA

Country Status (1)

Country Link
TW (1) TW567686B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7912011B2 (en) 2005-03-31 2011-03-22 Ntt Docomo, Inc. Radio communication system, base station, mobile station and wireless communication method
TWI381697B (en) * 2004-01-13 2013-01-01 Interdigital Tech Corp Code division multiple access (cdma) method and apparatus for protecting and authenticating wirelessly transmitted digital information

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI381697B (en) * 2004-01-13 2013-01-01 Interdigital Tech Corp Code division multiple access (cdma) method and apparatus for protecting and authenticating wirelessly transmitted digital information
US7912011B2 (en) 2005-03-31 2011-03-22 Ntt Docomo, Inc. Radio communication system, base station, mobile station and wireless communication method

Similar Documents

Publication Publication Date Title
KR100369791B1 (en) Apparatus and method for synchronizing channel in w-cdma communication system
US7126981B2 (en) Method and apparatus for cell search for W-CDMA with effect of clock offset
TW561729B (en) Method for cell search under effect of high clock offset
US20080244364A1 (en) Method And Apparatus For Code Group Identification And Frame Synchronization By Use Of Reed-Solomon Decoder And Reliability Measurement For UMTS W-CDMA
CN1856945B (en) Initial synchronization device and method for receivers
JP3473575B2 (en) CDMA mobile communication device and base station detection method used therefor
JP2001007734A (en) Code synchronization obtaining method for cdma communication system and apparatus thereof
JP2003189374A (en) Cell search system for mobile station in time division duplex system and method for the same
JP2006512825A (en) Cell search method and apparatus for mobile terminal of TDD-CDMA system
US8126092B2 (en) Multistage PN code acquisition circuit and method
US8761081B2 (en) Method and apparatus for cell searching in asynchronous CDMA systems
TW567686B (en) Method and apparatus for cell search for W-CDMA
JP2007531330A (en) Method and apparatus for detecting pilot signal with frequency offset using multi-stage correlator
US7480354B2 (en) Method and apparatus for channel estimation and cell search in cellular communication systems, and corresponding computer program product
Kim et al. DSA: A distributed sample-based fast DS/CDMA acquisition technique
TW567687B (en) Method and apparatus for cell search for W-CDMA with effect of clock offset
CN105071832B (en) A kind of high-speed frequency-hopping synchronous method for being independent of external clock benchmark
US7324585B2 (en) System and method for performing symbol boundary-aligned search of direct sequence spread spectrum signals
TWI232043B (en) Method and apparatus for cell search for W-CDMA with non-ideal sampling
Sriram et al. An analysis of the 3-stage search process in W-CDMA
Nielsen et al. WCDMA initial cell search
TW564649B (en) Method and apparatus for cell search under effect of high clock offset
Bahl Cell searching in WCDMA
EP1078473A1 (en) Multistage pn code acquisition circuit and method
Guey et al. Improving the robustness of target cell search in WCDMA using interference cancellation

Legal Events

Date Code Title Description
GD4A Issue of patent certificate for granted invention patent
MM4A Annulment or lapse of patent due to non-payment of fees