JPS63140960A - Detection of object of cell classifying device - Google Patents

Detection of object of cell classifying device

Info

Publication number
JPS63140960A
JPS63140960A JP28664686A JP28664686A JPS63140960A JP S63140960 A JPS63140960 A JP S63140960A JP 28664686 A JP28664686 A JP 28664686A JP 28664686 A JP28664686 A JP 28664686A JP S63140960 A JPS63140960 A JP S63140960A
Authority
JP
Japan
Prior art keywords
waveform
absorbancy
detection
single color
detected
Prior art date
Legal status (The legal status 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 status listed.)
Pending
Application number
JP28664686A
Other languages
Japanese (ja)
Inventor
Tadashi Abe
正 阿部
Hajime Matsushita
松下 甫
Riyouhei Yabe
矢辺 良平
Sumio Abe
阿部 寿美雄
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hitachi Ltd
Original Assignee
Hitachi Ltd
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 Hitachi Ltd filed Critical Hitachi Ltd
Priority to JP28664686A priority Critical patent/JPS63140960A/en
Publication of JPS63140960A publication Critical patent/JPS63140960A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obviate erroneous detection and mis-detection by obtaining the absorbancy waveform by the other single color which is largely different in the absorbancy of only the object to be detected from other cells and dirt in the addition to the absorbancy waveform by the single color and obtaining a difference therebetween. CONSTITUTION:A blood specimen smeared and dyed on slide glass is measured by a photoelectric conversion array mounted to a microscope. The absorbancy waveform (b) by the specific single color at D-D' is first obtd. at this time. Another absorbancy waveform (c) is then obtd. by the other single color which is largely different in the absorbancy of only the object A to be detected from the other cell B and dirt C in comparison with the absorbancy waveform (b). The difference between these two waveform signals is determined and the absorbancy waveform (d) is obtd. The waveform (d) is sliced at a level F-F' and is binary-coded. The influence of the cells and dirt except the object to be detected is thereby eliminated and the erroneous detection and mis-detection are obviated.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は細胞分類装置の対象物検出法に係り、特に血液
学分野の血液像自動分類装置における対象物の誤検出や
検出ミスをなくするのに好適な細胞分類装置の対象物検
出法に関するものである。
[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a method for detecting an object in a cell sorting device, and in particular, to eliminate false detection and detection errors of objects in an automatic blood image classification device in the field of hematology. The present invention relates to an object detection method for a cell sorting device suitable for.

〔従来技術〕[Prior art]

従来、顕微鏡画像入力をともなう画像計測において、複
数の単一色情報より対象物の検出を行っている例はなく
、単一色情報のみにて検出が行われていた。
Conventionally, in image measurement that involves inputting microscopic images, there has been no example of detecting an object using a plurality of single color information, and detection was performed using only single color information.

なお、白血球検出′3A置としては、特開昭53−81
94号公報で提案されたものがある。
In addition, for white blood cell detection '3A,
There is one proposed in Publication No. 94.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

上記従来技術は、誤検出や検出ミスの不都合が発生する
可能性があり、よい方法であるとはいえない。このこと
を第3図により説明する。顕微鏡視野のに得られている
のは、スライドガラスに塗抹、染色された血液標本の一
例であり、■は■のD−D’ における血液細胞の特徴
を最もよく表わすm−色に対する標本内の吸光度波形で
ある。この例で、白血球Aを検出しようとするとき、ス
ライドE−E’ は赤血球Bと白血球Aの広い部分との
中間にあり、両者を送別して白血球Aを検出している。
The above-mentioned conventional technology is not a good method because it may cause problems such as false detection or detection errors. This will be explained with reference to FIG. What is obtained in the microscopic field is an example of a blood specimen smeared and stained on a slide glass, and ■ indicates the color in the specimen for the m-color that best represents the characteristics of blood cells in DD' of ■. This is an absorbance waveform. In this example, when trying to detect white blood cells A, slide E-E' is located between red blood cells B and a wide area of white blood cells A, and both are separated to detect white blood cells A.

しかし、顕微鏡視野■内には、塗抹時あるいは染色時に
ごみCの付着は避けられずに散在しているので、この例
では、ごみCも同様に検出されてしまう。この不都合を
除く手段として、スライザE−E’ により2値化され
たごみCと白血球Aとの面積に着目し、その大小を判別
している。従来の方法では、スライザE−E’は必ず白
血球Aの広い部分と赤血球Bの範囲内になければならな
いといえる。吸光度波形@、スライザE−E’ とも、
光学的、電気的に変動要因を有し、この方法では常に安
定にしかも正確に白血球Aを赤血球BやごみCから送別
、検出することは非常に難しいといえる。第3図におい
て、スライザE−E’ と吸光度波形@が相対的に変動
し。
However, since dust C is unavoidably scattered within the microscope field of view during smearing or staining, dust C is also detected in this example. As a means to eliminate this inconvenience, attention is paid to the area of the garbage C and white blood cells A binarized by the slicer E-E', and the size thereof is determined. In the conventional method, it can be said that the slicer E-E' must be within a wide range of white blood cells A and red blood cells B. Both absorbance waveform @ and slider E-E'
Since there are optical and electrical fluctuation factors, it is extremely difficult to always stably and accurately separate and detect white blood cells A from red blood cells B and waste C using this method. In FIG. 3, the slider E-E' and the absorbance waveform @ vary relative to each other.

スライザE−E’ が赤血球Bをスライスするレベルに
なったときは、検出対象外の赤血球B細胞も検出してい
ることになり、装置の処理能力が著しく低下する不都合
が発生し、逆にスライスE−E’が白血球Aの狭い部分
をスライスするレベルに達したときは、白血球Aとごみ
Cの送別が困雛となる。場合によっては、小形の白血球
を特徴的に検出しないという不都合が発生するという欠
点を持っている。いずれの場合も、血液像分類装置にと
つて致命的な欠点となる。
When the slicer E-E' reaches the level where it can slice red blood cells B, it means that it has also detected red blood cell B cells that are not the detection target, which causes the inconvenience that the processing capacity of the device is significantly reduced, and vice versa. When E-E' reaches a level that slices a narrow portion of the white blood cells A, it becomes difficult to separate the white blood cells A and the waste C. In some cases, this method has the disadvantage of not characteristically detecting small white blood cells. In either case, this is a fatal drawback for the blood image classification device.

本発明の目的は、検出対象細胞の誤検出や検出ミスをな
くすことができる細胞分類装置の対象物検出法を提供す
ることにある。
An object of the present invention is to provide an object detection method for a cell classification device that can eliminate false detection and detection errors of detection target cells.

〔問題点を解決するための手段〕[Means for solving problems]

上記目的は、第2図に示すように、従来の単一色のみに
よる吸光度波形■と、この吸光度波形Oに対・して検出
対象物のみが他の細胞やごみと吸光度が大きく異なる他
の単一色より得られる吸光度波形のとの差分の吸光度波
形Oを得て、これをスライザF−F’で2値化して検出
するようにして達成するようにした。
As shown in Figure 2, the purpose of the above is to compare the conventional absorbance waveform ■ with only a single color and the absorbance waveform This is achieved by obtaining an absorbance waveform O which is the difference between the absorbance waveform obtained from one color and detecting it by converting it into a binary value using a slider FF'.

〔作用〕[Effect]

単一色のみによる吸光度波形は、血液細胞の特徴を最も
よく得られる吸光度波形であり、また、この吸光度波形
に対して検出対象物のみが他の細胞やごみの吸光度が大
きく異なるもう1つの単一色より得られる吸光度波形を
得て、この2つの吸光度波形の差を求めるようにしてい
るので、検出対象物である白血球のものは、赤血球やご
みのものがほぼ除去されるため、明瞭に抽出され、これ
をスサイサで2ft化した<a号は、スライザや上記2
つの吸光度波形の電気的、光学的な少々の変動に対して
も誤検出を生ずることがない。
The absorbance waveform using only a single color is the absorbance waveform that best captures the characteristics of blood cells.In addition, compared to this absorbance waveform, there is another single-color absorbance waveform in which only the detection target has a significantly different absorbance from other cells and dirt. Since the absorbance waveform obtained from the above is obtained and the difference between these two absorbance waveforms is determined, white blood cells, which are the detection target, are clearly extracted because red blood cells and dust are almost completely removed. , This was made into 2ft with a slider and the above 2.
Even slight electrical and optical fluctuations in absorbance waveforms will not cause false detection.

〔実施例〕〔Example〕

以下本発明の対象物検出法の一実施例を第1図を用いて
Jη細に説明する。
Hereinafter, one embodiment of the object detection method of the present invention will be described in detail with reference to FIG.

第1図は本発明の細胞分類装置の対象物検出法の一実施
例を説明するための装置構成説明図である。第り図にお
いて、顕微鏡Gの鋲頭部には顕微鏡画像取込み用のカラ
ーテレビカメラ1と第2図の吸光度波形@を得るための
半導体光電変換アレイJ及び吸光度波形○を得るための
半導体光電変換アレイKが取り付けである。半導体光電
変換アレイJ、にの出力は、差分増幅回路部りに送られ
、また、f−導体光電変換アレイJの出力はスライザM
にも送られ、スライザMでは、半導体光重変換アレイJ
の出力のスパン変動に対応したスライスレベルが決定さ
れる。差分増幅回路部りでは、半導体光電変換アレイJ
、にの信号を増幅し、I米光度波形面、のを作り、続い
て両信号の差分を取り吸光度波形Oを1!トる。また、
吸光度波形■に対してスライザMの出力F−F’でスラ
イスをかけ、最終出力を2値化された検出信号とする。
FIG. 1 is an explanatory diagram of the device configuration for explaining one embodiment of the target object detection method of the cell classification device of the present invention. In Figure 2, the rivet head of the microscope G is equipped with a color television camera 1 for capturing microscope images, a semiconductor photoelectric conversion array J for obtaining the absorbance waveform @ shown in Figure 2, and a semiconductor photoelectric conversion array for obtaining the absorbance waveform ○. Array K is the attachment. The output of the semiconductor photoelectric conversion array J is sent to the differential amplifier circuit section, and the output of the f-conductor photoelectric conversion array J is sent to the slicer M.
It is also sent to the semiconductor optical conversion array J in the slicer M.
The slice level corresponding to the span variation of the output is determined. In the differential amplifier circuit section, semiconductor photoelectric conversion array J
, to create the optical intensity waveform plane I, and then take the difference between the two signals to make the absorbance waveform O 1! Toru. Also,
The absorbance waveform (1) is sliced by the output FF' of the slicer M, and the final output is a binary detection signal.

ステージ制御部Nは、ステージ駆動部Pに作用し、細+
14fi本Sが乗せられたX、Y、ZステージRをx、
y、z方向に制御する。スライザMにより2値化された
最終出力が検出対象物を検出したと判断したときのステ
ージ制御部Nは、XYZステージRのXY方向は検出対
象物をカラーテレビカメラIの中央に移動させるように
制御し、2方向は自動焦点検出部Tの指令に基づき、合
焦点方向に制御する。
The stage control section N acts on the stage drive section P, and
X, Y, Z stage R on which 14fi book S is placed x,
Control in the y and z directions. When the final output binarized by the slider M determines that the object to be detected has been detected, the stage control unit N moves the object to be detected in the XY direction of the XYZ stage R to the center of the color television camera I. The two directions are controlled in the in-focus direction based on commands from the automatic focus detection section T.

本実施例によれば、誤検出がなく検出対象物を検出でき
るので、特異細胞を検出ミスすることによるデータネ良
を防ぎ、また、ごみや他の細胞等の異物検出がなくなる
ので、処理の亮速化をはかることができる。
According to this embodiment, the object to be detected can be detected without false detection, which prevents data errors caused by erroneously detecting specific cells, and also eliminates the detection of foreign substances such as dust or other cells, making processing easier. You can speed up the process.

〔発明の効果〕〔Effect of the invention〕

以上説明したように1本発明によれば、検出対象以外の
細胞やごみの影響をほぼ除去できるので。
As explained above, according to the present invention, the influence of cells and dust other than those to be detected can be almost eliminated.

誤検出や検出ミスがなく、正確で安定な対象物検出がで
きるという効果がある。
This has the effect of enabling accurate and stable object detection without false detection or detection errors.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明の細胞分類装置の対象物検出法の一実施
例を説明するための装置i!!構要説明図、第2図は本
発明の一実施例の説明図、第3図は従来技術の説明図で
ある。 G・・・顕微鏡、工・・・カラーテレビカメラ、J、K
・・・半導体光電変換アレイ、L・・・差分増幅回路、
M・・・スライザ、T・・自動焦点検出部、N・・・ス
テージ制御部、P・・・ステージ駆動部、R・・・XY
Zステージ、S・・・細胞標本。
FIG. 1 is a device i! for explaining an embodiment of the object detection method of the cell sorting device of the present invention. ! FIG. 2 is an explanatory diagram of an embodiment of the present invention, and FIG. 3 is an explanatory diagram of a prior art. G...Microscope, Engineering...Color television camera, J, K
...Semiconductor photoelectric conversion array, L...Differential amplifier circuit,
M...slizer, T...automatic focus detection unit, N...stage control unit, P...stage drive unit, R...XY
Z stage, S...Cell specimen.

Claims (1)

【特許請求の範囲】[Claims] 1、顕微鏡画像入力を行つて細胞分類を行うものにおい
て、複数の単一色情報より検出対象物の検出を行うとき
に、従来の単一色のみによる吸光度波形と、該吸光度波
形に対して前記検出対象物のみが他の細胞やごみと吸光
度が大きく異なる他の単一色より得られる吸光度波形と
の差分を得て、これをスライザで2値化して検出するよ
うにすることを特徴とする細胞分類装置の対象物検出法
1. In a system that performs cell classification by inputting microscopic images, when detecting a detection target based on multiple single color information, the conventional absorbance waveform using only a single color and the detection target based on the absorbance waveform are used. A cell sorting device characterized by obtaining the difference between absorbance waveforms obtained from other single colors in which only objects have absorbances that are significantly different from other cells and dirt, and detecting the difference by converting it into a binary value using a slider. object detection method.
JP28664686A 1986-12-03 1986-12-03 Detection of object of cell classifying device Pending JPS63140960A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP28664686A JPS63140960A (en) 1986-12-03 1986-12-03 Detection of object of cell classifying device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP28664686A JPS63140960A (en) 1986-12-03 1986-12-03 Detection of object of cell classifying device

Publications (1)

Publication Number Publication Date
JPS63140960A true JPS63140960A (en) 1988-06-13

Family

ID=17707120

Family Applications (1)

Application Number Title Priority Date Filing Date
JP28664686A Pending JPS63140960A (en) 1986-12-03 1986-12-03 Detection of object of cell classifying device

Country Status (1)

Country Link
JP (1) JPS63140960A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5187749A (en) * 1990-04-10 1993-02-16 Olympus Optical Co., Ltd. Virus infection examination apparatus having automatic determination function and method therefor
JP2002065884A (en) * 2000-09-04 2002-03-05 Yamato Protec Co Opener for gas group fire-extinguishing facility
EP1566625A1 (en) * 2004-02-23 2005-08-24 Ortho-Clinical Diagnostics, Inc. Method for determining an analyte by multiple measurements through a cuvette

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5187749A (en) * 1990-04-10 1993-02-16 Olympus Optical Co., Ltd. Virus infection examination apparatus having automatic determination function and method therefor
JP2002065884A (en) * 2000-09-04 2002-03-05 Yamato Protec Co Opener for gas group fire-extinguishing facility
EP1566625A1 (en) * 2004-02-23 2005-08-24 Ortho-Clinical Diagnostics, Inc. Method for determining an analyte by multiple measurements through a cuvette

Similar Documents

Publication Publication Date Title
US3851156A (en) Analysis method and apparatus utilizing color algebra and image processing techniques
US3999047A (en) Method and apparatus utilizing color algebra for analyzing scene regions
AU724393B2 (en) Method and apparatus for automated image analysis of biological specimens
US5787189A (en) Biological analysis system self calibration apparatus
US4362386A (en) Method and apparatus for recognizing smears
US11226280B2 (en) Automated slide assessments and tracking in digital microscopy
CA2228062C (en) Robustness of classification measurement
CN101685060A (en) Sample imaging apparatus
GB1426311A (en) Colour separation of discrimination in pattern recognition systems
US3963350A (en) Apparatus for selectively segmenting red and white blood corpuscles contained in blood smear
EP0088610B1 (en) Method for determination of percentage t cell content of lymphocyte
JPH03291567A (en) Virus infection inspecting device and virus infection inspecting method
US3893767A (en) Electro-optical system for cancellation of the effects of red blood cells in a sample of biological cells
JPS639864A (en) Automatic cell classifying device
JPS63140960A (en) Detection of object of cell classifying device
US4252425A (en) Camera focus detecting device
RUTOVITZ Automatic chromosome analysis
JPS6132182A (en) Device for classifying cell
US3970845A (en) Pulse discriminator circuit
US5233668A (en) Method and apparatus for discriminating aggregation pattern
JPS5830049B2 (en) Automatic reticulocyte measurement device
US4082457A (en) Leukocyte detector
DEW et al. An automatic microscope system for differential leukocyte counting
EP1210634B1 (en) Methods and devices in an optical system
JPS63231263A (en) Automatic classifying device for blood image