TWI232043B - Method and apparatus for cell search for W-CDMA with non-ideal sampling - Google Patents

Method and apparatus for cell search for W-CDMA with non-ideal sampling Download PDF

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TWI232043B
TWI232043B TW91105519A TW91105519A TWI232043B TW I232043 B TWI232043 B TW I232043B TW 91105519 A TW91105519 A TW 91105519A TW 91105519 A TW91105519 A TW 91105519A TW I232043 B TWI232043 B TW I232043B
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cell search
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Wern-Ho Sheen
Jan-Shin Ho
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Accton Technology Corp
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Abstract

The invention discloses a cell search method for a CDMA system for a three-stage cell search procedure. The cell search method has the steps of matching of incoming signals by a chip matched filter; over-sampling the incoming signals N times against a chip rate by a sampling device; transmitting the N over-samplers into a serial test unit, selecting a best sample among N over-samples by the serial test unit controlled by a first stage detector; and transmitting the best sample of the N over-samples into a second stage detector and a third stage detector for a trial. The best sample of the N over-samples has a maximum sampling value of the N over-samples. The invention significantly reduces the effects of non-ideal sampling so as to accomplish fast cell search.

Description

念|_r:案號 911gli _η 曰 修正 五、發明說明(1) 【發明所屬之技術領域 本發明係有關於一種用於分碼多工接取(c〇de 、 division multiple access (CDMA))系統之細胞搜尋方法 及裝置,更特別有關於一種用於寬頻分碼多工接取系統之 細胞搜尋方法及裝置,該方法及裝置藉由使用一細胞搜尋 演算法以降低系統中非理想取樣的效應。 【先前技術】 使用一直接序列型展頻之分碼多工接取技術的分碼多 工接取細胞式系統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 率的再利用性質’分碼多工接取系統之頻寬效率比起其他 多工接取系統(如分頻多工接取與分時多工接取)更加優 越。此外,細胞規劃在分碼多工接取系統係相當簡單。因 此,分碼多工接取細胞系統將是未來之主流。 第三代合作計畫(3 G P P )寬頻分碼多工接取/分頻雙工 (W-CDMA/FDD)系統已被採用於一種用於IMT-2000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 E )作為搜尋最佳細胞的方法係被稱為π細胞搜 尋”。快速的細胞搜尋係非常重要,為了減少該用戶裝置 父換延遲時間(switched-〇n delay)(初始搜尋),而增加 待機(s t a n d b y t i m e )(閒置狀態搜尋)及在話機時 (handover)(動作狀態aCtiVe mode搜尋)保持良好的通|| r: Case No. 911gli _η Revision V. Description of the invention (1) [Technical Field to which the Invention belongs] The present invention relates to a system for cod, division multiple access (CDMA) Cell search method and device, and more particularly, it relates to a cell search method and device for a wideband CDMA multiplexing access system. The method and device reduce the effect of non-ideal sampling in the system by using a cell search algorithm. . [Previous technology] The code division multiplexing access cellular system using a direct sequence spread spectrum multiplexing access technology greatly increases the channel capacity. This system has attracted considerable attention in recent research on mobile communication systems. Generally speaking, ‘due to the nature of frequency reuse’, the bandwidth efficiency of a code division multiplexed access system is better than other multiplexed access systems (such as frequency division multiplexed access and time division multiplexed access). In addition, cell planning in the code division multiplexing access system is fairly simple. Therefore, the code division multiplexed access system will be the mainstream in the future. The 3rd Generation Partnership Project (3 G P P) Wideband-Division Multiplexing Access / Division Duplex (W-CDMA / FDD) system has been adopted as one of the standards for the third-generation system of IMT-2000. In a cellular system of one-code multiplexed access, the method used by a user device (UE) to search for the best cell is called π-cell search. "A fast cell search system is very important. Switch-on delay (initial search), increase standby time (idle state search) and handover (operation state aCtiVe mode search) to maintain good communication

第7頁 ΐ 2 ι):案號 91105519_年月日__ 五、發明說明(2) 訊連結品質。 見於頒給Shou等人之美國專利號碼第6, 0 38, 2 5 0號, 其標題為π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π ( 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輸出之電功率,且輸出該結果至 長碼同步時程決定器(long code synchronization timing determiner)、門檻值計算器(threshold value calculator)及長碼驗證器(long 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。Page 7 ΐ 2 ι): Case No. 91105519_year month day__ 5. Description of the invention (2) Quality of information link. See U.S. Patent No. 6, 0 38, 250, issued to Shou et al., Entitled π Initialization Synchronization Method and Direct-Sequence Code Division Multiplexing Access Receiver Receiver for Asynchronous Cell System π (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 type code division multiplexing access repeater Synchronized 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 electric power of the relevant output of the matched filter, and outputs the result to a long code synchronization timing determiner, a threshold value calculator, and a long code verifier ( long code identifier). During the initial cell search, 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 of the N chips that make up a part of the synthesized spreading code sequence is sequentially replaced and output.

見於頒給Nystrom等人之美國專利號碼第6, 1 8 5, 244 唬,其標題為"細胞搜尋於分碼多工接取通訊系統”,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 碼計畫需要一長碼及碼框時程。一個具有M _ (M Q —訂丫) 2子長度的碼集合,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See U.S. Patent No. 6, 1 8 5, 244 issued to Nystrom et al., Whose title is "Cell Search in Code Division Multiplexing Access Communication System", revealed in Cell Search in Code Division Multiplexing Access Communication During the system, a more efficient encoding plan requires a long code and a code frame time history. A code set with a sub-length of M_ (MQ — subscription), where the codeword contains a set of Q short codes, The code set is defined to a specific characteristic. The initial characteristics that are satisfied are that the codeword has no cyclic drift and thus generates a valid codeword; the others are

滿足的特性為於長碼訊息與有效之碼字之間,且有一對一 應1 (mapping),且該編碼器將可發現出現在干擾盥雜訊 機移動(因而發現碼框時程)與該傳輸的碼字⑽即, 相關於長碼表示訊息(long c〇de indicat丨⑽ message))’具有某些程度上的精確與合理的複雜度。 挪%,於頒給Klm等人之美國專利號碼第6, 2 8 9, 0 0 7號,其 2,為”一個在非同步分碼多工接取行動通訊系統之獲得 寻、’、田肊基地台的方法,揭示一群碼與細胞碼係多工傳 輸=且被使用作一引導碼對於有差別的基地台於非同步細 胞分碼多工接取通訊系統;使用多工傳輸碼,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 =系,之獲得搜尋細胞基地台的方法包含一基地台控制 :、複數個行動台及基地台、和使用不同序列之不同基地 台,該搜尋細胞基地台的方法之步驟包含(a)指定該細胞 ,群碼作為基地台的同相(丨n p h a s e )通道之引導碼(匕)指定 κ、’田胞之群碼作為基地台的正交(q u a d r a t u r e )通道之引導 碼多工傳輸該同相(inphase)通道與正交(quadrature: 通道之引導碼及產生一同相與正交之引導碼。 現請參考第一圖,該圖將有助於了解一第三代合作計 晝(3GPP)寬頻分碼多工接取/分頻多工系統之簡化碼框結 構。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來 元成’邊二階段係包含兩個獨特設的同步通道及一個共同 的引導通道。在第一階段1丨〇中,初級(pr i mary )同步通 道(PSCH) 1 1 1係用於時槽(si〇t)同步。該初級同步通道The satisfying characteristic is that there is a one-to-one 1 (mapping) between the long code message and the valid code word, and the encoder will find that it appears to interfere with the movement of the messenger (thus the time frame of the code frame) and The transmitted codeword (ie, long code representation message) has a certain degree of accuracy and reasonable complexity. No. 6, in U.S. Patent No. 6, 28, 0, 0, 7 issued to Klm et al., "2," is the acquisition of a mobile communication system using asynchronous code division multiplexing access.肊 Base station method, revealing that a group of codes and cell codes are multiplexed = and used as a guide code. For different base stations, asynchronous communication is used for multiplexed access to the communication system; using multiplexed codes, interference Reduced due to the use of two pilot codes. One method for obtaining a cell base station in asynchronous multiplexing access is to include a base station control: a plurality of mobile stations and base stations, and the use of different For different base stations in sequence, the method of searching for a cell base station includes (a) specifying the cell, and the group code as the guide code (d) of the in-phase (丨 nphase) channel of the base station, and specifying the group code of κ and 'field cell The pilot code of the quadrature channel of the base station multiplexes the pilot code of the inphase channel and the quadrature: channel and generates the pilot code of the same phase and the quadrature channel. Please refer to the first figure, The figure will help to understand the simplified code frame structure of a 3rd Generation Cooperative Computing (3GPP) broadband frequency division multiplexing access / division multiplexing system. First of all, in the 3rd Generation Cooperative Computing (3Gpp) wideband frequency division In the code multiplexed access / frequency division multiplexed system, the cell search system typically uses three stages to form the 'edge two stage system, which includes two uniquely set synchronization channels and a common guidance channel. In the first stage, In 1 丨 〇, the primary (pr i mary) synchronization channel (PSCH) 1 1 1 is used for time slot (siot) synchronization. The primary synchronization channel

a 丨1 ( =± 1 )係 111包含有初級同步螞(PSC)定義為acp,其中 依賴在基地台傳送的多樣性傳送(diversi ty 打311^4。〇11)存在而定。在第二階段12〇中,次 道(SSCH) 121係用於碼框/碼群(c〇de gr〇up)辨識。 級同步通道121係包含有次級同步碼(SSCs)定義為acs,其 中係數cs係相似於初級同步通道之係數。在第三階段} 3、〇 中,該共同引導通道(CPICH) 131係用於下傳混亂&碼 (scrambling code)之決定。如圖所示,在1〇 (毫秒碼 框中包含了 15個時槽(slots),並且因為在該系統中使用 每秒3.8 4百萬碼片(肘(:1^03/36(:)的速度。因此,有384〇〇a 丨 1 (= ± 1) system 111 contains the primary synchronization ant (PSC) defined as acp, which depends on the existence of the diversity transmission (diversi ty 311 ^ 4. 〇11) transmitted at the base station. In the second stage 120, the secondary channel (SSCH) 121 is used for code frame / code group (code gr0up) identification. The secondary synchronization channel 121 contains secondary synchronization codes (SSCs) defined as acs, where the coefficient cs is similar to that of the primary synchronization channel. In the third stage} 3, 0, the common guidance channel (CPICH) 131 is used for the decision of downloading the scrambling code. As shown in the figure, 15 slots are included in the 10 (millisecond code box), and because this system uses 3.84 million chips per second (elbow (: 1 ^ 03/36 (:) Speed. So, there is 384〇〇

個碼片在每一個碼框且2 5 6 0碼片在每一個時槽。此外,該 初級同步通道與該次級同步通道係2 5 6個碼片常且僅在該/ 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。該依序 式搜尋在下一個新的搜尋開始之前,需要一個接_個地依 序經過三個同步階段。比起導管式(pi pel ined)搜尋,依 序式(s e r i a 1 )搜尋通常花了更多的時間。導管式 (p i p e 1 i n e d )搜尋之三個階段可以同時地操作,因此可以 減少搜尋時間,當然,必須付出高複雜度的昂貴代價及計 算功率。 ' 現請參考第二圖’該圖係一用於傳統三階段依序式細 胞搜尋演算法之簡化圖。為簡化起見,一完整的三階段搜 哥將被稱之為^一個試驗(t r i a 1 )。在依序式細胞搜尋中,There are chips in each frame and 256 chips in each time slot. In addition, the primary synchronization channel and the secondary synchronization channel are 256 chips often and only transmitted at the beginning of the / time slot boundary. / The traditional cell search of 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 catheter Pipelined search. The sequential search needs to go through three synchronization stages one after the other before the next new search starts. A sequential search (s e r i a 1) search usually takes more time than a pi pel ined search. The three stages of the ducted (p i p e 1 i n e d) search can be operated simultaneously, so the search time can be reduced. Of course, a high cost of complexity and computational power must be paid. 'Please refer to the second figure' This figure is a simplified diagram for a traditional three-stage sequential cell search algorithm. For simplicity, a complete three-stage search will be referred to as a trial (t r i a 1). In sequential cell search,

第10頁 \4imm , i I ή 丨哼號 91105519_年月日_«_ 五、發明說明(5) 試驗並不重疊,直到該搜尋成功為止,也就是說,在一時 間内只能有一個階段(即方框2 1 1、方框2 1 2與方框2 1 3 )在 動作,因此消耗較低的功率損失,但花費更長的搜尋時 間。 另一方面,參考第三圖,該圖係一用於傳統三階段導 管式細胞搜尋演算法之簡化圖。在導管式搜尋,不同階段 之檢測係同時操作,且試驗係重疊的。也就是,方框 3 1 1、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,在一個固定的時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。過去,只有該導管式搜尋較令人感興趣。 需注意對導管式搜尋而言,比起依序式細胞搜尋並沒有額 外的硬體裝置係需要的。實際上,一個試驗的整體過程時 間並不需要30毫秒(ms),如圖所示。(Κ +2 )χ 10 (ms)的該細 胞搜尋時間係被要求於每一次搜尋,如果該細胞搜尋在第 K次試驗成功。 然而,一般基本的假設常使用於第三代合作計畫 (3GPP)寬頻分碼多工接取/分頻多工之細胞搜尋之先前技 術中。也就是,在碼片-匹配濾波器輸出之取樣係完美的 (理想取樣)。實際上,在碼片-匹配濾波器輸出之取樣係 不是完美的(即非理想取樣)。該非理想取樣將減低訊號雜 訊比且增加該細胞搜尋時間。由於該非理想取樣,該細胞 搜尋之操作特性係被嚴重地破壞。 【發明内容】Page 10 \ 4imm, i I ή 丨 91 91519519_ 年月 日 _ «_ V. Description of the invention (5) The experiments do not overlap until the search is successful, that is, there can be only one at a time. Phases (ie, blocks 2 1 1, 2 2, and 2 1 3) are in operation, and therefore consume lower power loss, but take longer search time. On the other hand, referring to the third figure, this figure is a simplified diagram for a conventional three-stage catheterized cell search algorithm. In catheterized search, detection at different stages is performed simultaneously, and tests are overlapped. That is, boxes 3 1 1, 3 2 1 and 3 3 1 are in the same test. Obviously, in the guided search, there are more possible tests in a fixed time, and therefore a faster search is obtained. Of course, the price paid is greater power consumption. In the past, only this ducted search was more interesting. It should be noted that for catheterized search, there is no additional hardware device required than sequential cell search. In fact, the overall process time of an experiment does not require 30 milliseconds (ms), as shown in the figure. The cell search time of (K +2) χ 10 (ms) is required for each search if the cell search succeeds in the Kth test. However, the general basic assumptions are often used in the previous technology of the 3rd Generation Partnership Project (3GPP) wideband CDMA multiplexed access / frequency multiplexed cell search. That is, the sampling at the chip-matched filter output is perfect (ideal sampling). In fact, the sampling system at the chip-matched filter output is not perfect (ie, non-ideal sampling). The non-ideal sampling will reduce the signal-to-noise ratio and increase the cell search time. Due to the non-ideal sampling, the operational characteristics of the cell search were severely disrupted. [Summary of the Invention]

彦號 91105519 年月曰__修正 五、發明說明(6) 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, 以降低非理想取樣效應及快速完成細胞搜尋。 本發明之次要目的係提供一種用於細胞搜尋裝置,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’以在非理想取樣效應下實現細胞搜尋且不增加硬體的 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,藉由使用一種新的細胞 搜尋演算法,該方法中使用三個階段的通道係在第三代合 作計畫(3GPP)標準。其中第一階段具有一初級同步通道 (PSCH)係用於時槽同步;第二階段具有次級同步通道 (S S C Η )係在時槽同步後,用於碼框/碼群辨識;且第三階 段具有共同引導通道(CPICH)係用於下傳混亂碼之決定; 該細胞搜尋方式包含下列步驟:接收到的訊號首先通過碼 片匹配濾波器(ch ip matched fi Iter),並且針對訊號 7 > 中取樣頻率為N倍碼片速率(chip rate)。此 ^赴母N個連續取樣點中,在每隔固定時間内隨機變更取 別”此Γ卜做ί後續訊號檢測器之輸入,並據此進行訊號檢 例之訊號檢測器共分三階段。在第一階段訊 二、· ·° 了主要是偵測初級同步通道(PSCH)的時序 g 由於初級同步通道與時槽同步,因此告初鈒 同步通道的瞎皮、;丄 u此田子刀級 f序破確定,則同時完成時槽同步。緊接著,Yan No. 91105519 January __Revision V. Description of the invention (6) The main purpose of the present invention is to provide a cell search method for a code division multiplexing access system, and more particularly for a wideband code division multiplexing access. System to reduce non-ideal sampling effects and quickly complete cell searches. A secondary object of the present invention is to provide a cell search device for a code division multiplexing access system, and more particularly for a wideband code division multiplexing access system 'to realize cell search under non-ideal sampling effects and Does not increase 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 for a wideband code division multiplexing access system to reduce non-ideal sampling effects. A new cell search algorithm that uses a three-stage channel system in the 3rd Generation Partnership Project (3GPP) standard. The first phase has a primary synchronization channel (PSCH) for time slot synchronization; the second phase has a secondary synchronization channel (SSC Η) for code frame / code group identification after time slot synchronization; and the third The stage has a common guidance channel (CPICH) for the decision to transmit the scrambled code. The cell search method includes the following steps: the received signal first passes through a chip matched filter (ch ip matched fi Iter), and the signal 7 > The medium sampling frequency is N times the chip rate. In this case, the N consecutive sampling points are randomly changed at regular intervals to determine whether the signal detector is used as the input of subsequent signal detectors, and the signal detectors for signal inspection are divided into three stages. In the first phase, the second phase is mainly to detect the timing of the primary synchronization channel (PSCH). Because the primary synchronization channel is synchronized with the time slot, the blindness of the synchronization channel is reported at the beginning. If the sequence is broken, the time slot synchronization is completed at the same time.

發明說明(7) 二階段訊號偵測器基於初級、 先 辨 群 同 偵 :匕 次 次級同步通道偵㈨。由於次級二:道的時序’進-步進 經過蝙碼,此編碼過後的訊J 8步通道承載的訊號皆預 識。因此,當完成第二階俨=可以提供作為碼框及碼群 同步。此外,第三階段訊=^唬檢測,即能完成碼框碼 步,以及第二階段的碼框以用j你依’,,、弟卩白奴的時槽 測。其中,第三階段選取的、3碼群同步,以進行混亂碼 較。若選取的混亂碼低於此:亂碼將進一步與一門檻值 三階段檢測。反之,則此—門檻值,則重新啟動另一 進一步確認。當混IL碼通過同J亂碼進入一同步驗證單元 取的混亂碼即被接受,反之 V驗證早凡的檢測後,則選 由於同步驗證單元處理時妒=重啟另一次三階段檢測。 遲時間τ產秒(ms))。因此,1長(在本說明書中假設為延 無法通過同步驗證單元。則亂碼通過第一次門檻但卻 間,將大幅降低系統效能 同步驗證單元中所耗費的時 下二本取發:Λ方法之一特徵,其中在沒有干擾出現 有最大的取樣值'之該最佳取樣點係在該_取樣點中具 夺统本ΐ::Ϊ供—種細胞搜尋裝置,用於分碼多工接取 士個ρ上 於寬頻分碼多工接取系、統,該裝置處理 其中第一階段具有一初級同步通道 PSCH係用於時槽同步;第二階段具有次級同步通道 /SCH係在時槽同步後,用於碼框/碼群辨識;且第三階 段具有共,引導通道(CPICH)係用於下傳混亂碼之決定; 讜細胞搜尋裝置包含:一碼片匹配濾波器,用以匹配一進 ^ 案號 91105519 !423i(W3 i 二-:一 曰 五、發明說明(8) ^ ^---feL _ 入信號;一取樣元件,連結於該石馬片匹_ 該進入信號以一碼片速率過取樣N次·-己據波器,用以將 s a m p 1 e r ),連結於該取樣元件,用以傳〜樣器(d 〇 w η -點;一依序測試單元,連結於該降取梯f為_過取樣 過取樣點中選擇一最大取樣點;一繁— 用以在该Ν個 於該依序測試單元,用於得到第一階===測裔,連接 二階段檢測器,連結至該依序測試單元,用以得到碼群f 碼框同步;一第三階段檢测器,連結至該依序測試單元了 用以決定一混亂碼;以及一認證單元,連結於該第三階段 檢測器’用於決定該試驗是否成功。 該認證單元更包含:一比較器,連結至該第三階段檢 測器,用以測試該第三階段之輸出值與一門檻值”此較; 第一決定元件,連接至該比較器,用以決定該混亂碼是 否正碟,其中如果該門檻值被超過,則所選之混亂碼即進 入一同步驗證單元,否則該試驗視為失敗,且一新試驗在 =延遲下將重新開始;該同步驗證單位,連結至該第一決 定元件,用以驗證該混亂碼;以及一第二決定元件,連接 至該同步驗證單位,用以決定該混亂碼是否接受;其中如 果f混氣碼通過該第二決定元件,則試驗係成功,否則一 新f驗在一延遲時間T麾秒(m s )後重新開始,且在匹配濾 波器之取樣點係假設是均勻分布的。 下根據本發明之裝置之一特徵,其中在沒有干擾出現 ’違N過取樣點中之該最佳取樣點係在該N過取樣點中具 有最大的取樣值。 本發明之其他特徵與優點將從下文詳細的描述、所附Description of the invention (7) The two-stage signal detector is based on the primary, pre-identified group co-detection: dagger-time secondary synchronization channel detection. Because the sequence of the second level: track's step-by-step passes through the bat code, the signal carried by the 8-step channel after the encoding is predicted. Therefore, when the second order is completed, 俨 = can be provided as code frame and code group synchronization. In addition, the third phase of the message = ^ detection, that is, the code frame code step can be completed, and the second phase of the code frame to use the time slot test of the Jieyi ’, the younger brother. Among them, the 3 code group selected in the third stage is synchronized to perform chaotic code comparison. If the selected scramble code is lower than this: the scramble code will be further detected with a threshold and three stages. Otherwise, if this is the threshold value, another further confirmation is started. When the mixed IL code enters a synchronous verification unit through the garbled code of J, the scrambled code taken is accepted. Otherwise, after V verifies the earlier detection, it is selected because the synchronous verification unit processes jealousy = restarts another three-stage detection. Late time τ produces seconds (ms)). Therefore, 1 long (it is assumed in this description that the delay cannot pass the synchronization verification unit. The garbled code passes the first threshold but at the same time, it will greatly reduce the time spent in the synchronization verification unit to obtain two copies: Λ method One of the features, where the best sampling point where no interference occurs is the best sampling point in the _ sampling point, which has the standard ΐ :: Ϊ supply-a cell search device for code division multiplexing Take the number ρ on the wideband code division multiplexed access system. The device processes the first stage with a primary synchronization channel PSCH for time slot synchronization; the second stage has a secondary synchronization channel / SCH at time After slot synchronization, it is used for code frame / code group identification; and in the third stage, the common channel (CPICH) is used for the decision of transmitting scrambled codes; 谠 The cell search device includes: a chip matched filter for Match one advance ^ Case No. 91105519! 423i (W3 i two-: one fifth, invention description (8) ^ ^ --- feL _ input signal; a sampling element, connected to the stone horse piece _ A chip rate is oversampled N times. samp 1 er), connected to the sampling element, used to pass ~ sampler (d 〇w η-points; a sequential test unit, connected to the descending ladder f is _ oversampling oversampling points to choose a maximum sampling Point; a complex — for the N sequential testing units for obtaining the first order === test family, connecting a two-stage detector, connecting to the sequential testing unit for obtaining the code group f Code frame synchronization; a third-stage detector connected to the sequential test unit to determine a scrambled code; and an authentication unit connected to the third-stage detector 'to determine whether the test was successful. The The authentication unit further includes: a comparator connected to the third-stage detector to test the output value of the third stage and a threshold value "this comparison; a first determining element connected to the comparator to determine Is the scramble code correct? If the threshold is exceeded, the selected scramble code enters a synchronous verification unit, otherwise the test is considered a failure and a new test will be restarted with the delay; the synchronous verification Unit, linked to that first decision A determining element for verifying the scramble code; and a second determining element connected to the synchronous verification unit for determining whether the scramble code is accepted; wherein if the f-mixed gas code passes the second determining element, the test is successful Otherwise, a new f-test is restarted after a delay time T 麾 seconds (ms), and the sampling points of the matched filter are assumed to be uniformly distributed. A feature of the device according to the present invention, in which no interference occurs 'The optimal sampling point in the N oversampling point has the largest sampling value in the N oversampling point. Other features and advantages of the present invention will be described in detail below and attached.

案號 91105Fi1Q 年月曰 修正- 五、發明說明(9) 圖示和所界定的專利範圍而顯而易見。 【實施方式】 該第一階段依序測試方法之主要觀念係該被選擇的最 佳取樣點具有該N過取樣點的最大取樣值。該在第一階段 中所選擇出來之最佳取樣點在非理想取樣被考慮時,能增 進操作特性。 現請參考第四圖,該圖係顯示根據本發明之一種細胞 搜尋方法,該方法係使用第一階段依序測試方法。根據本 I明’總數個5 1 2混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。每個碼係3 8 4 〇 〇個碼片長且係因此擴展到 整個碼框。由於該細胞位置並不同步,該碼總是在該碼框 邊界處開始其新的週期。如第四圖所示,該方法中處理三 個階段的過程。其中第一階段4丨〇具有一初級同步通道 fPSCH)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^ 者’ 一般化等級制度的葛雷序列(general ized hierarchical Golay seqUence)由於易於實現,係被使 作為該初級同步碼。第二階段4 2 〇具有次級同步通道 (SSCH)係在時槽同步後,用於碼框/碼群辨識。同步盥 群辨識可以藉由檢測該次級同步通道而達到,其中哕、·… 係被1 6個正交展頻碼之一個所展頻,稱之為次級同g碼。' 雕麵3:R! 车 丨! η索號 ^ ,一____________ ; 五、發明說明'(10) 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(丨5,3 )之無間斷 里德-所羅門碼(comma —f ree Reed s〇1⑽㈣c〇de, CFRS) ’其中該組之每一碼字被表成一碼群。因為無間段 ^良好特性,一旦碼群被指定,則該碼框同步係完成。第 三階,430具有共同引導通道(cpiCH)係用於下傳混亂瑪 之决疋。在孩碼群被指定後,藉由選擇一群中8個碼之_ 個,經由使用共同引導通道,該混亂碼係可簡單地被決 定。 、 第五圖係顯示根據本發明之實施例之一種細胞搜尋方 法之流私圖’該方法係使用第一階段依序測試(s e厂丨a ^ /n ,STS1 )方法。為敘述該流程,第六圖亦 而"、、、口 第/、圖係顯示根據本發明之一種細胞搜尋架構, 該架構係使用第一階段依序測試(serial test in stage —Case No. 91105Fi1Q Month, Amendment-V. Description of Invention (9) The illustrations and defined patent scope are obvious. [Embodiment] The main idea of the first-stage sequential testing method is that the selected best sampling point has the maximum sampling value of the N oversampling point. The optimal sampling point selected in the first stage can increase the operating characteristics when non-ideal sampling is considered. Please refer to the fourth figure, which shows a cell searching method according to the present invention, which uses the first stage sequential testing method. According to the present invention, a total of 5 1 2 scramble codes are used in different cells at the time of downloading and are used repeatedly in the entire system. The code is subdivided into 64 groups, each group has 8 codes. Each code is 3 840 chips long and is therefore extended to the entire code frame. Since the cell positions are not synchronized, the code always starts its new cycle at the border of the code frame. As shown in the fourth figure, this method deals with three stages. The first stage (4) has a primary synchronization channel (fPSCH) for time slot synchronization. By using the same primary synchronization channel at each seek and by sending 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. Furthermore, the generalized hierarchical Golay sequence (generalized hierarchical Golay seqUence) is used as the primary synchronization code because it is easy to implement. The second stage 4 2 0 has a secondary synchronization channel (SSCH) which is used for code frame / code group identification after time slot synchronization. Synchronous group identification can be achieved by detecting the secondary synchronization channel, where 哕, ... are spread by one of the 16 orthogonal spreading codes, which is called secondary iso-g code. 'Carved face 3: R! Car 丨! η cable number ^, one ____________; 5. Description of the invention '(10) In order 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, using a (5, 3) uninterrupted Reed-Solomon code (comma —f ree Reed s〇1⑽㈣c〇de, CFRS) 'where each codeword of the group is represented as a code group. Because of the good characteristics of the non-interval segment, once the code group is specified, the code frame synchronization system is completed. The third stage, 430 has a common guide channel (cpiCH), which is used to pass down the chaos of chaos. After the child code group is specified, by selecting one of 8 codes in the group, the chaotic code system can be simply determined by using a common guidance channel. The fifth diagram is a private diagram of a cell search method according to an embodiment of the present invention. The method uses a first-stage sequential test (s e) a ^ / n, STS1 method. To describe the process, the sixth diagram also shows the cell search architecture according to the present invention, which uses a serial test in stage—

第16頁 1 ’ STSl)方法。如圖,該架構係使用第一階段依序測試 ^serial test in stage-卜 STS1)方法。一種細胞搜尋裝 夕2 0 0,用於分碼多工接取系統,更特別係用於寬頻分碼 夕工f取系統,該裝置處理三個階段之通道。一碼片匹配 慮波器2 1 0,一取樣元件2 2 0連結於該碼片匹配濾波器 ^1〇’ 一降取樣器(down-sampler) 2 3 0連接至該取樣元件 2 〇 ’ 一依序測試單元2 4 5連接該取樣器2 3 〇,一第一階段 ,測器2 4 0連接於該依序測試單元2 4 5,一第二階段檢測器 姓5〇連結至該依序測試單元245,一第三階段檢測器26〇連 、、、。至該依序測試單元245,一認證單元28〇連結於該第三階 .¾涵· [;索號91105519 年月日 倏π: 五、發明說明(11) 段檢測器2 6 0。該認證單元2 8 0更包含一比較器2 7 〇連結至 該第三階段之檢測器2 6 0,一第一決定元件2 7 5連接至^亥比 較器2 7 0,一同步驗證單元2 9 0連結至該第一決定元件〆 2 7 5,以及一第二決定元件2 9 5連接於該同步驗證單位 2 9 0 〇 現請參照第五圖與第六圖。在步驟6 0 0中,該匹配滤 波器2 1 0,位於該細胞搜尋裝置2 0 0之前端,用以檢測一進 入h號1 9 0之波形。在步驟6 1 0中,該取樣元件2 2 0,將該 進入信號1 9 0以碼片速率過取樣N次,且該過取樣後信號表 示成Yi(k), Y2(k),、 、 、YN(k),並送入一降取樣器230。 在步驟615中,該降取樣器(d〇wn-sampler)230,將該N個 過取樣#號傳送至該依序測試單元2 4 5,且由該第一階段 之檢測器2 4 0控制之該依序測試單元2 4 5在該N個過取樣後 信號中選取最佳取樣點。在步驟6 2 0中,該依序測試單元 2 4 5 ’將該最佳取樣點傳送至第二階段檢測器2 5 〇與第三階 段之檢測器2 6 0。在第一階段之方框4 1 1,第二階段之方框 4 2 1與第三階段之方框4 3丨(見第四圖)係測試相同選擇的 最佳取樣點’其中該最佳取樣點係在N個過取樣點中有最 大之取樣值,因此可以減低非理想取樣的效應。一旦該試 驗錯誤’下一個新試驗將再次測試隨機選取的取樣點。在 第一階段之方框,第二階段之方框與第三階段之方框亦將 測試相同選擇的最佳取樣點。如此的試驗將一直進行,直 到混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,且對每一個試驗需要(Ν + 2)χ 1〇毫秒 (m s )’因此若整個細胞搜尋在第κ次試驗才成功,所需的Page 16 1'STSl) method. As shown in the figure, the architecture uses the first stage sequential test method (STS1) method. A cell search device is used in a code division multiplexing access system, and more particularly is used in a wideband code division system. The device processes three stages of channels. A chip matching filter 2 1 0, a sampling element 2 2 0 is connected to the chip matching filter ^ 1 ′, a down-sampler 2 3 0 is connected to the sampling element 2 0 ′, a The sequential test unit 2 4 5 is connected to the sampler 2 3 0, a first stage, the tester 2 40 is connected to the sequential test unit 2 45, a second-stage detector surname 50 is connected to the sequential Test unit 245, a third-stage detector with 260, ,,, and. Up to the sequential test unit 245, an authentication unit 28o is connected to the third stage. ¾ han · [; cable number 91105519 month day 月 π: 5. Description of the invention (11) Segment detector 260. The authentication unit 2 0 0 further includes a comparator 2 7 0 connected to the third stage detector 2 60, a first determining element 2 7 5 is connected to the comparator 2 7 0, and a synchronous verification unit 2 90 is connected to the first determining element 〆 27.5, and a second determining element 295 is connected to the synchronous verification unit 2 900. Please refer to the fifth and sixth figures. In step 600, the matched filter 210 is located at the front end of the cell search device 2000, and is used to detect a waveform entering the number 190 of h. In step 6 10, the sampling element 2 2 0 oversamples the incoming signal 1 90 at a chip rate N times, and the signal after the oversampling is expressed as Yi (k), Y2 (k),,, , YN (k), and send it to a down-sampler 230. In step 615, the down-sampler 230 transmits the N oversampling # numbers to the sequential test unit 2 4 5 and is controlled by the first stage detector 2 4 0 The sequential test unit 2 4 5 selects the best sampling point among the N oversampled signals. In step 6 2 0, the sequential testing unit 2 4 5 ′ transmits the optimal sampling point to the second-stage detector 250 and the third-stage detector 26 0. Box 4 1 1 in the first stage, box 4 2 1 in the second stage, and box 4 3 丨 in the third stage (see the fourth figure) are tested for the same best selected sampling point 'where the best The sampling point has the largest sampling value among the N oversampling points, so the effect of non-ideal sampling can be reduced. Once the test is wrong, the next new test will test the randomly selected sampling points again. In the first phase of the box, the second phase of the box and the third phase of the box will also test the best sampling point for the same selection. Such tests will continue until the scramble code is accepted by the synchronous verification process. What's more, the selection of the sampling points is realized sequentially, and each test requires (N + 2) χ 10 milliseconds (m s) ’. Therefore, if the whole cell search is successful in the κth test, the required

格 麵酶 5Γ、簽兩说H12) #號 91105519 年 修正 細胞搜尋時間是(K + N + 1 )x 1 0毫秒(m s )。 在步驟6 3 0中,第一階段檢測器2 4 0用於得到第一階段 之時槽同步。一非同調的(non-coherent)匹配濾波器,其 中該匹配濾波器係分為複數個區段,且每一區段之輸出係 以其絕對質合併,係被分成四個區塊且作為一被使用在第 一階段3 1 0中作為時槽同步之一檢測器。非一致的累積超 過15時槽係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 超過一個時槽的邊界被選擇進入下一個階段。Grid enzyme 5Γ, signed two said H12) # No. 91105519 year correction The cell search time is (K + N + 1) x 10 milliseconds (m s). In step 6 30, the first stage detector 240 is used to obtain the time slot synchronization of the first stage. A non-coherent matched filter, where the matched filter is divided into a plurality of sections, and the output of each section is merged with its absolute quality, divided into four blocks and used as a It is used as a detector for time slot synchronization in the first stage 3 10. The non-uniform cumulative slot system is properly found as additive white Gaussian noise beyond 15 hours. For better characteristics, the boundary of more than one time slot in the first stage is selected to enter the next stage.

在步驟6 4 0中,在時槽同步後,該碼群與碼框同步可 以在第二階段中完成。該第二階段檢測器2 5 〇使用丨6個匹 配濾、波器去檢測該次級同步碼。在第二階段之該一致的累 積(the coherent accumulation)係可能的藉由使用來自 第一階段之該通道估計。在集合了 1 5個次級同步碼後,它 們係相關於該6 4 C F R S碼字,每一碼字有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,在第三階段,一策略係使用於檢 測該混亂碼,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。基本上,在第三階段中,該第三階段 檢測器2 6 0在該階段係選擇一混|L碼。該第三階段檢測器 26 0係由8個主動相關偵測可能的混亂碼立中每隔2 片,第三階段檢測器就做一次判斷,並選取8個主動相關 偵測器中最大值所相對應的混亂碼紀錄一次最後,經過 150次紀錄後(一個碼框長度),該最大得票數之值系係送In step 64, after the time slot synchronization, the code group and code frame synchronization can be completed in the second stage. The second-stage detector 25 uses 6 matching filters and wave detectors to detect the secondary synchronization code. The coherent accumulation in the second stage is possible by using the channel estimates from the first stage. After collecting 15 secondary synchronization codes, they are related to the 6 4 C F R S codeword, and each codeword 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 with respect to the maximum value are determined as reasonable code group and code frame boundaries, respectively. In step 650, in the third stage, a strategy is used to detect the scrambled code by selecting one of eight codes in a group, wherein the code group has been identified in the second phase. Basically, in the third stage, the third stage detector 260 selects a mixed | L code at this stage. The third-stage detector 260 is composed of eight active correlation detection probable confusion codes every two slices. The third-stage detector makes a judgment and selects the maximum value among the eight active correlation detectors. The corresponding chaotic code is recorded once and finally, after 150 records (one code frame length), the value of the maximum number of votes is sent

;;案號 91105519 A_η 修正 五、發明說明(13) 至一認證單元去決定該試驗是否正確。該最大得票數之值 與一門檻值77此較。該門檻值77 (/系根據常數錯誤警報速 率(constant false alarm rate)來決定。在步驟 660中, 來自該第三階段檢測器2 6 0之該輸出2 6 1係與一門檻值 〇2 7 1作測試比較。該第一決定元件2 7 5,在該比較器2 7 0 之後,用以決定該混亂碼是否正確。如果該門檻值未被超 過,該試驗視為失敗,且一新試驗在不延遲下將重新開 始。如果該門檻值被超過,該混亂碼即進入該同步驗證單 元 2 9 0。 在步驟6 7 0中,該第二決定元件2 9 5,驗證該混亂碼是 否接受,其中如果該混亂碼通過該第二決定元件2 9 5,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,且在匹配濾波器之一初始取樣點係假設是均勻 分布的。 廣泛的電腦模擬係使用於探討該新細胞搜尋演算法與 傳統方法之操作特性之比較。此處強調非理想取樣之效 應。所有的數值結果係依據,N = 2,最大的都普勒飄移 係185. 2赫茲(100-km/hr),每一階段的檢測係10毫秒 (ms),Ί> 2 5 0毫秒 (ms)且 7/ 〇係以10—之錯誤警報值來設 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,且該共同引 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,該共同引導通道之功率係為總傳輸 功率之10 %。換句話說,在細胞搜尋過程中,總傳輸功率 之8 0係貢獻在細胞内干擾。最後,一幾何因子(geometry;; Case No. 91105519 A_η Amendment 5. Invention description (13) to a certification unit to determine whether the test is correct. The value of the maximum number of votes is compared with a threshold value of 77. The threshold value 77 (/ is determined according to a constant false alarm rate. In step 660, the output 2 6 1 from the third-stage detector 2 6 0 is in accordance with a threshold value 0 2 7 1 for test comparison. The first decision element 275 is used after the comparator 270 to determine whether the scramble code is correct. If the threshold is not exceeded, the test is considered a failure and a new test It will restart without delay. If the threshold is exceeded, the scramble code enters the synchronization verification unit 290. In step 6 70, the second decision element 2 95 verifies whether the scramble code is accepted , If the scramble code passes the second decision element 2 95, the test is successful, otherwise a new test is restarted after a delay time T p milliseconds (ms), and the initial sampling point of one of the matched filters is It is assumed to be uniformly distributed. Extensive computer simulations are used to explore the comparison of the operating characteristics of the new cell search algorithm with traditional methods. The effect of non-ideal sampling is emphasized here. All numerical results are based on N = 2. Doppler drift system is 185.2 Hz (100-km / hr), each stage of the detection system is 10 milliseconds (ms), Ί > 2 50 milliseconds (ms) and 7 / 〇 is a 10-error alarm In addition, the transmission power of the actual channel is expressed as follows. First, the primary synchronization channel and the secondary synchronization channel have the same power, and the common guidance channel and the synchronization channel (primary synchronization channel + secondary synchronization channel) The power ratio is fixed. Second, the power of the common guidance channel is 10% of the total transmission power. In other words, during the cell search process, 80% of the total transmission power contributes to intracellular interference. Finally, a 1. geometric factor

第19頁 SS9U05519 年 曰 修正 五、發明說明(14) factor) GWPbPpsch+p ssch+Ppc)/p X係使用於模組化該用戶裝 置在細胞中之位置。愈高的G值,表示該用戶裝置愈靠近 該基地台附近。搜尋時間的蓄積的分布函數(CDF )係用來 探討不同搜尋演算法之特性指標。 現請參考第七圖,該圖係顯示根據本發明,在非理想 取樣效應下之一種信號模型。使用一基頻(base-band)表 示,該接收到之信號r (t)係被給定為: Γ(ί) = Σ]Α/ν^〇(ί) + ^550(ί)+^ρς(ί)μ - iTc ~τ) + Λ^ηι(ί)) <^,〇 + V^nx(t) (EQ -1) 其中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頻 碼。g ( τ,t)係表示雷利衰減增益之複數值,h (t)係一上 升餘弦函數之平方根(SqUare root raised cosine shaping function)並具有一粗略因子約〇·22。Tc係該用 戶裝置之碼片期間。r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 (-〇. 5Tc,0· 5Tc)之間均勻 地分布。此外’ P與P孫分別為細胞内干擾η I (t)與細胞間 干擾η χ( t)之功率,其中η丨(t )與n x( t)係以具有單一變數之 零均白色向斯雜訊(zero mean additive white Gaussian noise with unity variance)來模組化。 根據數學式E Q - 1所示,亦可表示為: ⑼ + \^Sssc(t) + KSpc⑴j+ 此―)丨 x 的,0 + v^nx(t)Page 19 SS9U05519 Years Amendment 5. Explanation of the invention (14) factor) GWPbPpsch + p ssch + Ppc) / p X is used to modularize the position of the user device in the cell. A higher G value indicates that the user equipment is closer to the base station. The cumulative distribution function (CDF) of the search time is used to explore the characteristics of different search algorithms. Please refer to the seventh figure, which shows a signal model according to the present invention under non-ideal sampling effects. Using a base-band representation, the received signal r (t) is given as: Γ (ί) = Σ] Α / ν ^ 〇 (ί) + ^ 550 (ί) + ^ ρς (ί) μ-iTc ~ τ) + Λ ^ ηι (ί)) < ^, 〇 + V ^ nx (t) (EQ -1) where Ppsc, Cpsc, pssc, Cssc and Ppc, cpc are respectively Primary synchronization channel 'The power and spreading code of the secondary synchronization channel and the common pilot channel. g (τ, t) is a complex value representing the Rayleigh attenuation gain, h (t) is a square root of a raised cosine function (SqUare root raised cosine shaping function) and has a rough factor of approximately 0.22. Tc is the chip period of the user device. r is an initial random delay and is modeled with a random variable. The variable has a uniform distribution across the entire (-0.5Tc, 0.5Tc). In addition, P and P are the powers of intracellular interference η I (t) and intercellular interference η χ (t), where η 丨 (t) and nx (t) are zero white with a single variable. Noise (zero mean additive white Gaussian noise with unity variance). According to the mathematical formula E Q-1, it can also be expressed as: ⑼ + \ ^ Sssc (t) + KSpc⑴j + this ―) 丨 of x, 0 + v ^ nx (t)

案號 91105519 年月曰 修正 五、發明說明(15) (EQ-2), 其中 psc、 (t) = c psc( i)x h(t-iTc-r ) S ssc( t ) — C ssc(Case No. 91105519 Rev. V. Description of Invention (15) (EQ-2), where psc, (t) = c psc (i) x h (t-iTc-r) S ssc (t) — C ssc (

h(t-iTc-T (EQ-3) (EQ-4) sh (t-iTc-T (EQ-3) (EQ-4) s

\)y cpc(i) x h(t-iTc-r ) (EQ-5), 上述模型有三個觀察係值得在此提出。首先,為了簡化, 只考慮平坦的衰落通道,且只有有關於該細胞搜尋之通道 才清楚地處理;所有其他的通道係被包含在干擾項η !(t)或 n x( t)之内了。第二,r係表示為非理想取樣之效應,這是 過去先前技術所忽略的,且第三,該模型假設該效應係來 自於震盪器之不穩定之相同頻率源。 第八圖係顯示在非理想取樣效應下,比較不同細胞搜 尋方法之特性圖。其中"理想π係用來表示理想取樣。如 圖所示,非理想取樣造成嚴重的操作特性破壞,特別係在 較低的信號雜訊比SNR的案例中(一較小的G值)一種較實 際的例子。在此圖中,對所有的演算法及信號雜訊比增益 G為6dB時,9 0 %的機會(occas i ons )會在1 1 0毫秒内被完 成。另一方面,在信號雜訊比增益G為OdB時,本發明之方 法STS1在3 0 0毫秒内完成90 %的搜尋率,但是對傳統演算 法卻花了 4 5 0毫秒(ms)。需注意,在非常低比例的搜尋目\) y cpc (i) x h (t-iTc-r) (EQ-5). There are three observation systems of the above model that deserve to be proposed here. First, for simplicity, only flat fading channels are considered, and only those channels that are searched by the cell are dealt with clearly; all other channels are included in the interference term η! (T) or n x (t). Second, r is expressed as the effect of non-ideal sampling, which was ignored in the prior art, and third, the model assumes that the effect is from the same frequency source of instability of the oscillator. The eighth graph is a graph showing the comparison of different cell search methods under the non-ideal sampling effect. Where " ideal π is used to represent ideal sampling. As shown in the figure, non-ideal sampling causes severe damage to operating characteristics, especially in the case of lower signal-to-noise ratio (SNR) (a smaller G value), a more practical example. In this figure, for all algorithms and signal-to-noise ratio gain G of 6dB, a 90% chance (occas i ons) will be completed in 110 milliseconds. On the other hand, when the signal-to-noise ratio gain G is OdB, the method STS1 of the present invention completes a search rate of 90% in 300 milliseconds, but it takes 450 milliseconds (ms) for the traditional algorithm. Please note that in a very low percentage of searches

第21頁 _麵3 Π 案號 91105519 ± 曰 修正 五、發明說明(16) 標CDF下,傳統的演算法之特性較佳,這可以歸因於在較 少的機會中(〇 c c a s i ο n s ),在傳統演算法之取樣系較接近 最佳化的點。 雖然本發明已就其較佳實施例解釋說明,由上述 知,吾人可知多數的修正與變化可以被實現而不會脫離本 發明之原始目的精神與創新的觀念。需瞭解的是,所示之 特定具體實施例並非意圖或意味著用以限制本發明;所揭 示者係意圖包含所附加的專利範圍且所有的修正將落入專 利範圍的領域。Page 21_face 3 Π Case No. 91105519 ± Amendment V. Description of Invention (16) The traditional algorithm has better characteristics under the standard CDF, which can be attributed to fewer opportunities (〇ccasi ο ns) Sampling in traditional algorithms is closer to the point of optimization. Although the present invention has been explained in terms of its preferred embodiments, from the above, we can see that most of the modifications and changes can be realized without departing from the spirit of the original purpose of the present invention and the concept of innovation. It should be understood that the specific embodiments shown are not intended or meant to limit the invention; the disclosed are intended to encompass the scope of the appended patent and all amendments will fall within the scope of the patent.

第22頁Page 22

修正 牌夕::Ϊ係、顯示一用於第三代合作計畫(3GPP)之寬頻分 馬夕工接取Λ刀頻多工系統之簡化碼框結構圖。 夕工^圖二f/ 一用於第三代合作計畫(3GPP)寬頻分碼 ^工接取刀,夕工系統之傳統的依序式細胞搜尋方法。 (在此例中,母一階段之過程時間係設為為1〇毫秒(^)) 第三圖係顯示一用於第三代合作計晝(3GPP)寬頻分碼 多工接取/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(ms )) 第四圖係顯示根據本發明之一種細胞搜尋方法,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 n s t a g e - 1, STS1)方法。 第五圖係顯示根據本發明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。 第六圖係顯示根據本發明之一種細胞搜尋架構’該架 構係使用第一階段依序測試方法。 第七圖係顯示根據本發明之一種信號模型。 第八圖係顯示在非理想取樣效應下,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 1 9 0 信號Modification: Xixi :: Display and display a broadband code division for the 3rd Generation Partnership Project (3GPP). Ma Xigong receives the simplified code frame structure diagram of the Λ knife frequency multiplexing system. Xi Gong ^ Figure 2 f / One is used for the 3rd Generation Partnership Project (3GPP) broadband frequency division code. Gong takes the knife, the traditional sequential cell search method of the Xi Gong system. (In this example, the process time of the first stage is set to 10 milliseconds (^)) The third picture shows a multi-frequency access / frequency division for 3rd Generation Cooperative Computing (3GPP) wideband code division Traditional ducted cell search method for multiplexed systems. (In this example, the process time of each stage is set to 10 milliseconds (ms)) The fourth diagram shows a cell search method according to the present invention, which uses the first stage sequential test (seria 1 testinstage-1, STS1) method. The fifth diagram is a flowchart of a cell search method according to the present invention, which uses the first stage sequential testing method. The sixth diagram shows a cell search architecture according to the present invention. The architecture uses a first-stage sequential testing method. The seventh diagram shows a signal model according to the present invention. The eighth graph is a graph showing the comparison of different cell search methods under the non-ideal sampling effect. Explanation of drawing number: 111 primary synchronization channel 121 secondary synchronization channel 131 common guidance channel 1 9 0 signal

I 案號 91105519 曰 修正 245 250 260 270 271 275 280 290 295 圖式簡單說明 2 0 0 細胞 2 10 碼片 2 2 0 取樣 2 3 0 降取 2 4 0 第一 依序 第二 第三 比較 門檻 第一 認證 一同 第二 搜尋裝置 匹配濾波器 元件 樣器 階段檢測器 測試單元 階段檢測器 階段檢測器 器 值π 0 決定元件 一 早兀 步驗證單元 決定元件I Case No. 91105519 Amendment 245 250 260 270 271 275 280 290 295 Schematic description 2 0 0 Cell 2 10 Chip 2 2 0 Sampling 2 3 0 Drop 2 4 0 A certification together, a second search device, a matched filter element, a sampler, a phase detector, a test unit, a phase detector, and a detector value π 0.

第24頁Page 24

Claims (1)

Ί'::Γ -- 二.ί 土. Ί'mm.w 蒙號 91105519 A_ 修正 六、申請專利範圍 1. 一種用於分碼多工接取系統之細胞搜尋方法,該方 法中用於三個階段之細胞搜尋過程,該細胞搜尋方式包含 下列步驟: 藉由一碼片匹配濾波器,匹配(m a t c h )—進入信號; 藉由一取樣元件,將該進入信號以碼片速率過取樣N 次; 藉由一降取樣器(d 〇 w η - s a m p 1 e r ),將該N個過取樣信 號傳送至一依序測試單元; 藉由被一第一階段檢測器控制之該依序測試單元在 該N過取樣點中選取一最佳取樣點;並 傳送該N個過取樣點中之被選取之最佳取樣點至一第 二階段檢測器及一第三階段檢測器以完成一個 試驗(t r i a 1 )。 2 .依申請專利範圍1之細胞搜尋方法,其中該細胞搜 尋之該試驗更包含下列步驟: 藉由第一階段之檢測器,可得到第一階段之時槽同 步; 藉由一第二階段之檢測器,檢測該碼群與碼框同 步; 藉由一第三階段之檢測器,選擇一混亂碼; 藉由一比較器,測試該混亂碼與一門檻值7?此較; 藉由一在該比較器後之一第一決定元件決定該混亂 碼; 其中如果該門檻值被超過,則所選之混亂碼即進入Ί ':: Γ-II. Ί 土. Ί'mm.w Mongolian No. 91105519 A_ Amendment VI. Patent Application Scope 1. A cell search method for a code division multiplexing access system. The cell search process at this stage includes the following steps: a chip matching filter, match (incoming signal); by a sampling element, the incoming signal is oversampled N times at a chip rate ; By a down-sampler (d 0w η-samp 1 er), the N oversampling signals are transmitted to a sequential test unit; by the sequential test unit controlled by a first-stage detector at A best sampling point is selected from the N oversampling points; and the selected best sampling point from the N oversampling points is transmitted to a second stage detector and a third stage detector to complete a test (tria 1 ). 2. The cell search method according to the scope of the patent application 1, wherein the test of the cell search further includes the following steps: With the detector of the first stage, the time slot synchronization of the first stage can be obtained; The detector detects that the code group is synchronized with the code frame; by a third-stage detector, a scramble code is selected; by a comparator, the scramble code is compared with a threshold value of 7? The first decision element behind the comparator determines the scramble code; wherein if the threshold value is exceeded, the selected scramble code enters 第25頁 l_._r 索號 91105519 曰 修正 六、申請專利範圍 且 一同步驗證單元,否則該試驗視為失敗 新試驗在不延遲下將重新開始;以及 藉由一在該同步驗證單元後之一第二決定元件決定 該混亂碼; 其中如果該混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Τ產秒(ms ) 後重新開始,且在匹配濾波器之一初始取樣點 係假設是均勻分布的。 ,其中該N過取樣 係在該N過取樣 ,其中得到第一 係使用一般化 3 .依申請專利範圍1之細胞搜尋方法 點中之該最佳取樣點在沒有干擾出現下 點中具有最大的取樣值。 4 .依申請專利範圍2之細胞搜尋方法 階段之時槽同步更包含下列步驟: 該第一檢測器在一初級同步通道中 等級制度的葛雷序列(g e n e r a 1 i z e d hierarchical Go 1 ay sequence)作為一初級同 步碼。 5 .依申請專利範圍2之一種細胞搜尋方法,其中得到 第二階段之碼群及碼框同步更包含下列步驟: 該第二檢測器在一次級同步通道中,係使用與初級 同步碼正交之1 6個次級同步碼。 6 .依申請專利範圍5之細胞搜尋方法,其中該次級同 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 m m a - f r e e R e e d S ο 1 〇 m ο n c 〇 d e,Page 25 l _._ r Request No. 91105519 Amendment VI. Patent application scope and a synchronous verification unit, otherwise the test is deemed to fail and the new test will be restarted without delay; and by one after the synchronous verification unit The second decision element determines the scramble code; if the scramble code passes the second decision element, the test is successful; otherwise, a new test is restarted after a delay time T production second (ms), and the An initial sampling point is assumed to be uniformly distributed. Where the N oversampling is at the N oversampling, where the first is obtained using the generalization 3. The best sampling point among the cell search method points according to the scope of the patent application has the largest point in the absence of interference Sampling value. 4. The time slot synchronization according to the stage of the cell search method according to the scope of the patent application 2 further includes the following steps: The first detector has a genera 1 ized hierarchical Go 1 ay sequence in a primary synchronization channel as a Primary synchronization code. 5. A cell search method according to the scope of the patent application, wherein the second phase of code group and frame synchronization includes the following steps: The second detector is used in a secondary synchronization channel, which is orthogonal to the primary synchronization code. 1 of 16 secondary synchronization codes. 6. The cell search method according to the scope of the patent application 5, wherein the secondary synchronization channel is further encoded into a group of 64 code words by a (1,5,3) uninterrupted Reed-Solomon code (c 0 mma -free R eed S ο 1 〇m ο nc 〇de, 第26頁 曰 修正 六、申請專利範圍 CFRS),其中該組之每一碼字被表成一碼群,以辨識一碼 框邊緣及碼群。 7 ·依申請專利範圍2之細胞搜尋方法,其中在該碼群 被辨識後,該混亂碼可以經由使用共同引導通道,選擇8 個碼字之一個來決定。 8.依申請專利範圍2之細胞搜尋方法,其中該取樣點 之選擇係被依序地實現,且對每一個試驗需要(N + 2 )x 1 0毫 秒,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 + Ν +1 )x 1 0毫秒(m s )。 9 ·依申請專利範圍2之細胞搜尋方法,其中該第一階 段檢測器使用一非同調合成匹配濾波器在第一階段中執行 時槽同步。 1 0 .依申請專利範圍4之細胞搜尋方法,其中該第一階 段檢測器在該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選,雖然僅有一候選將被考慮到。 1 1 .依申請專利範圍5之細胞搜尋方法,其中該第二階 段檢測器使用1 6個匹配濾波器用作該次級同步碼之檢測。 1 2 .依申請專利範圍6之細胞搜尋方法,其中在第二階 段之該碼群與碼框邊界係為該碼群與該循環的移動位置之 最大值。 1 3.依申請專利範圍2之細胞搜尋方法,其中該門檻值 β 〇係根據常數錯誤警報速率(constant false alarm rat e )來決定。 1 4.依申請專利範圍1之細胞搜尋方法,其中該細胞搜Page 26 (Amendment VI. Patent Application Scope (CFRS)), where each codeword of the group is listed as a code group to identify a code frame edge and code group. 7. The cell search method according to the scope of patent application 2, wherein after the code group is identified, the chaotic code can be determined by using a common guidance channel and selecting one of 8 code words. 8. The cell search method according to the scope of the patent application, wherein the selection of the sampling points is realized sequentially, and (N + 2) x 10 milliseconds are required for each test, so if the entire cell search is performed at the Kth time The experiment was successful, and the required cell search time was (K + Ν +1) x 10 milliseconds (ms). 9. The cell search method according to claim 2 wherein the first stage detector uses a non-homogeneous synthetic matched filter to perform time slot synchronization in the first stage. 10. The cell search method according to patent application scope 4, wherein the first stage detector selects more than one time slot boundary in the primary synchronization code as a candidate for a better operation, although only one candidate will be considered . 11. The cell search method according to claim 5 wherein the second-stage detector uses 16 matched filters for detecting the secondary synchronization code. 12. The cell search method according to the scope of the application patent 6, wherein the boundary between the code group and the code frame in the second stage is the maximum value of the movement position of the code group and the cycle. 1 3. The cell search method according to the scope of patent application 2, wherein the threshold β 〇 is determined according to a constant false alarm rat e. 1 4. The cell search method according to the scope of application for patent 1, wherein the cell search 第27頁 1丨多、 ¢1212043^ 索號 91105519 年 修正 六、申請專利範圍 取/分頻雙工系統。 搜尋方法,其中該細胞搜 個人數位化助理(PDA)系 統之細胞搜尋裝置,該裝 二階段與第三階段)之細胞 配一進入信號; 匹配濾波器,用以將該 取樣N次; |,連結於該取樣元件, _ 尋方法係使用於寬頻分碼多工接 1 5.依申請專利範圍1之細胞 尋方法係使用於行動裝置與無線 統。 1 6 . —用於分碼多工接取系 置處理三個階段(第一階段、第二 搜尋,該細胞搜尋裝置包含: 一碼片匹配濾波器,用以匹 一取樣元件,連結於該碼片 進入信號以一碼片速率過 一降取樣器(down-sampler: 用以傳送該N個過取樣點; 降取樣器,用以在該N個 取樣點; 該依序測試單元,用於 一依序測試單元,連結於該 過取樣點中選擇一最大 一第一階段檢測器,連接於 得到第一階段之時槽同步; 一第二階段檢測器,連結至該依序測試單元,用以 得到碼群與碼框同步; 一第三階段檢測器,連結至該依序測試單元,用以 決定一混亂碼;以及 一認證單元,連結於該第三階段檢測器,用於決定 該試驗是否成功。 1 7.依申請專利範圍1 6之細胞搜尋裝置,其中該認證 單元更包含:Page 27 1 丨 Multiple, ¢ 1212043 ^ No. 91105519 Amendment VI. Patent Application Scope Fetch / Frequency Duplex System. A search method, in which the cell searches a cell search device of a personal digital assistant (PDA) system, and the cells of the second stage and the third stage are equipped with an entry signal; a matched filter is used to sample the N times; |, Connected to the sampling element, the _ finder method is used for wideband CDMA multiplexing1 5. The cell finder method according to the scope of patent application 1 is used for mobile devices and wireless systems. 1 6. — For the three stages of code division multiplexing access processing (first stage, second search, the cell search device includes: a chip matched filter for matching a sampling element, connected to the The chip-in signal passes a down-sampler at a chip rate (down-sampler: used to transmit the N oversampling points; a down-sampler is used at the N sampling points; the sequential test unit is used for A sequential test unit is connected to the over-sampling point to select a largest first-stage detector, which is connected to the time slot to obtain the first stage; a second-stage detector is connected to the sequential test unit, and To obtain the code group and frame synchronization; a third-stage detector connected to the sequential test unit to determine a scrambled code; and an authentication unit connected to the third-stage detector to determine the test Whether it is successful. 1 7. The cell search device according to the scope of application for patent 16, wherein the authentication unit further includes: 第汾頁 1ιΜθ#3·: 乐 ^±t 案號 91105519 Λ_η 曰 修正 六、申請專利範圍 一比較器,連結至該第三階段檢測器,用以測試該 第三階段之輸出值與一門檻值77此較; 一第一決定元件,連接至該比較器,用以決定該混 亂碼是否正確; 其中如果該門檻值被超過,則所選之混亂碼即進入 一同步驗證單元,否則該試驗視為失敗,且一 新試驗在不延遲下將重新開始; 該同步驗證單位,連結至該第一決定元件,用以驗 證該混亂碼;以及 一第二決定元件,連接至該同步驗證單位,用以決 定該混亂碼是否接受; 其中如果該混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Τ產秒(m s ) 後重新開始,且在匹配濾波器之一初始取樣點 係假設是均勻分布的。 1 8 .依申請專利範圍1 6之細胞搜尋裝置,其中該N過取 樣點(Y K k ), Y 2( k ),、、、Y N( k ))中之該最佳取樣點在沒有 干擾出現下,係該N過取樣點中具有最大的取樣值。 1 9.依申請專利範圍1 7之細胞搜尋裝置,其中該第一 階段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 s e q u e n c e )作為一初級同步碼。 2 0 .依申請專利範圍1 7之細胞搜尋裝置,其中該第二 階段檢測器在一次級同步通道中,係使用與初級同步碼正Fen page 1ιΜθ # 3 ·: Le ^ ± t Case No. 91105519 Λ_η Revision 6. Patent application scope a comparator connected to the third stage detector to test the third stage output value and a threshold value 77 comparison; a first decision element connected to the comparator to determine whether the scramble code is correct; wherein if the threshold value is exceeded, the selected scramble code enters a synchronization verification unit, otherwise the test Failed, and a new test will be restarted without delay; the synchronous verification unit is connected to the first determining element to verify the scramble code; and a second determining element is connected to the synchronous verification unit, using To determine whether the scramble code is accepted; wherein if the scramble code passes the second decision element, the test is successful; otherwise, a new test is restarted after a delay time T production second (ms), and one of the matched filters is The initial sampling points are assumed to be uniformly distributed. 18. The cell search device according to the scope of application for patent 16, wherein the optimal sampling point among the N oversampling points (YK k), Y 2 (k),, YN (k)) appears without interference. In the following, the N sampling point has the largest sampling value. 19. The cell search device according to the scope of patent application 17, wherein the first-stage detector uses a generalized hierarchical Golay sequence (eq u e n c e) as a primary synchronization code in a primary synchronization channel. 20. The cell search device according to the scope of application patent 17, wherein the second-stage detector is in a secondary synchronization channel and uses the same synchronization with the primary synchronization code. 第29頁Page 29 六、申請專利範圍 交之1 6個次級同步碼。 2 1 .依申請專利範圍1 7之細胞搜尋裝置,其中該次级 ^步通道更進一步被編碼成一組6 4碼字,藉由一(1 5,3 )之 …、間斷里德—所羅門石馬(comma-free Reed Solomon code, CFRS),其中該組之每一碼字被表成一碼群,以辨識一碼 框邊緣及碼群。 ^ 2 2 ·依申請專利範圍1 7之細胞搜尋裝置,其中在該碼 4被辨識後’該混亂碼可以經由使用共同引導通道,選擇 8個碼字之—個來決定。 ψ 2 3 ·依申請專利範圍1 6之細胞搜尋裝置,其中該取樣 ΐ ^選擇係被依序地實現’且對每一個試驗需要(N + 2 )x 1 〇 =I抽,t若整個細胞搜尋在第κ次試驗才成功,所需的 ' ^哥時間是(Κ + Ν + 1)χ 10毫秒(ms)。 階段:4測依丄請專利範圍1 7之細胞搜尋裝置,其中該第-行時槽同^用一非同調合成匹配濾波器在第一階段中執 •依申請專利範圍 階段檢剛5! / 4 …^不- 界作為一^ ί初級同步碼中選擇超過一個以上之時槽 該第一階=彳木作之候選,雖然僅有—候選將被考慮到 時槽逢界=t測器在該初級同步碼中選擇超過一個以上 慮到。下為—較佳操作之候選,雖然僅有一候選將被 階段Sixth, the scope of patent application is over 16 secondary synchronization codes. 2 1. The cell search device according to the scope of patent application 17 in which the secondary ^ step channel is further encoded into a group of 64 code words, with one (1, 5, 3) ..., intermittent Reed-Solomon stone A horse (comma-free Reed Solomon code, CFRS), where each codeword of the group is represented as a code group to identify a code frame edge and code group. ^ 2 2 According to the cell search device of patent application scope 17, after the code 4 is identified, the chaotic code can be determined by selecting one of 8 code words by using a common guidance channel. ψ 2 3 · The cell search device according to the scope of application patent 16 where the sampling ΐ ^ selection is realized in sequence 'and each test requires (N + 2) x 1 〇 = I pumping, t if the entire cell The search was successful only in the κ trial, and the required time is (K + Ν + 1) x 10 milliseconds (ms). Phase: 4 test cell search device according to patent scope 17, where the -time slot is identical in the first stage with a non-homogeneous synthetic matching filter … ^ No-Jie as a ^ ί choose more than one time slot in the primary synchronization code. The first order = candidate for Tochigi, although only-the candidate will be considered when the time slot meets the limit = t tester in the Choose more than one in the primary synchronization code to take into account. Below is-candidate for better operation, although only one candidate will be staged mM&rn ) ! ί 一 ΐ ;案號 91105519 曰 修正 六、申請專利範圍 測。 2 7 ·依申請專利範圍2 1之細胞搜尋裝置,其中在第二 階段之該碼群與碼框邊界係為該碼群與該循環的移動位置 之最大值。 2 8 .依申請專利範圍1 7之細胞搜尋裝置,其中該門檻 值77 系根據常數錯誤警報(constant false alarm rate) 來決定。 2 9 .依申請專利範圍1 6之細胞搜尋裝置,其中該細胞 搜尋方法係使用於寬頻分碼多工接取/分頻雙工系統。 3 0 .依申請專利範圍1 6之細胞搜尋裝置,其中該細胞 搜尋方法係使用於行動裝置與無線個人數位化助理 PDA 系統。mM & rn)! ί One ΐ; Case No. 91105519, Amendment 6. Scope of patent application. 27. The cell search device according to the scope of application patent 21, wherein the boundary between the code group and the code frame in the second stage is the maximum value of the movement position of the code group and the cycle. 2 8. The cell search device according to the scope of patent application 17, wherein the threshold value 77 is determined according to a constant false alarm rate. 29. The cell search device according to the scope of application for patent 16, wherein the cell search method is used in a wideband division code multiplexed access / frequency division duplex system. 30. The cell search device according to the scope of application for patent 16, wherein the cell search method is used in a mobile device and a wireless personal digital assistant PDA system. 第31頁Page 31
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