Journal of Pathology Informatics

: 2018  |  Volume : 9  |  Issue : 1  |  Page : 16-

A method for the interpretation of flow cytometry data using genetic algorithms

Cesar Angeletti 
 Logical Cytometry, Atlanta GA, USA

Correspondence Address:
Dr. Cesar Angeletti
Logical Cytometry, 3324 Peachtree Rd #1408, Atlanta, GA 30326


Background: Flow cytometry analysis is the method of choice for the differential diagnosis of hematologic disorders. It is typically performed by a trained hematopathologist through visual examination of bidimensional plots, making the analysis time-consuming and sometimes too subjective. Here, a pilot study applying genetic algorithms to flow cytometry data from normal and acute myeloid leukemia subjects is described. Subjects and Methods: Initially, Flow Cytometry Standard files from 316 normal and 43 acute myeloid leukemia subjects were transformed into multidimensional FITS image metafiles. Training was performed through introduction of FITS metafiles from 4 normal and 4 acute myeloid leukemia in the artificial intelligence system. Results: Two mathematical algorithms termed 018330 and 025886 were generated. When tested against a cohort of 312 normal and 39 acute myeloid leukemia subjects, both algorithms combined showed high discriminatory power with a receiver operating characteristic (ROC) curve of 0.912. Conclusions: The present results suggest that machine learning systems hold a great promise in the interpretation of hematological flow cytometry data.

How to cite this article:
Angeletti C. A method for the interpretation of flow cytometry data using genetic algorithms.J Pathol Inform 2018;9:16-16

How to cite this URL:
Angeletti C. A method for the interpretation of flow cytometry data using genetic algorithms. J Pathol Inform [serial online] 2018 [cited 2021 Apr 12 ];9:16-16
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In the last decades, flow cytometry immunophenotyping has become the method of choice for the differential diagnosis of reactive and neoplastic hematologic disorders.[1] Routinely, 3–10 or more single tube combinations of monoclonal antibodies are used to characterize the different cellular populations in a wide range of biological specimens including blood, bone marrow tissue, body fluids, and lymph nodes.[2] This technology can be performed on solid tissues, but a single-cell suspension needs to be prepared previously. The initial step in flow cytometry analysis is data acquisition, where several tens of thousands of cells are measured in a few seconds and stored as very large sets of digitalized data. As an example, a file containing information on six parameters, when performed on 6 × 104 cells, creates a data set containing 3.6 × 105 coded numbers.[3] With the continuous discovery of new cell markers and the trend to more targeted therapies, it is conceivable that these number will increase exponentially. To manage such quantities of data, a computer is physically connected to the flow cytometer, and specialized software handle the digital interface. Through the adjustment of a series of physical conditions by the flow cytometer operator (e.g., voltage and compensation) appropriate acquisition is achieved. The compiled data are usually written and read in the form of the Flow Cytometry Standard (FCS) files, which are organized in the form of a large matrix of intensities over wavelengths versus events.[4] Almost every event will be a single cell, with rare occasional doublets (pairs of cells which pass the laser closely together). For each event, the measured fluorescence intensity indicates the amount of fluorescent-tagged antibodies directed to specific biomarkers, and therefore, a proxy for the amount of such biomarker in one cell. The ultimate interpretation of flow cytometry data is typically performed on a series of two-dimensional plots, where an experienced operator selects subpopulations of interest and interprets distributional patterns through visual examination.[5] The analysis can be time-consuming and subjective, sometimes involving intuition rather than standardized statistical inference. Depending on expertise, a certain cell population can be misidentified, overestimated or underestimated. The problem is compounded by the limited number of tagging fluorophores that can be analyzed simultaneously due to overlapping spectra, although the recent development of mass cytometry may greatly overcome this issue in the future.[6] Finally, there is a cost related side. Medicare reimbursement of each flow cytometry professional interpretation with 16 markers or more (CPT code 88189) was proposed to be $92.6 in 2017.[7]

Although flow cytometry interpretation is generally performed on series of two-dimensional image plots, it should be imagined in a multi-dimensional space where each dimension corresponding to a biological marker. Thus, every sample could be projected onto an n-dimensional space where each dimension is represented by a specific antigen. This fact encouraged researchers in search of mathematical analyses that can scale highly multidimensional data without significant impact on computation time.[8] Among these are cluster analysis,[9] principal component analysis,[10] and support vector machines.[11]

Genetic programming is a framework for the development of executable programs using evolutionary computing methods.[12] It relies on flexible optimization methods inspired by the theory of evolution of natural systems. Many different problems from different domains have been successfully tackled using evolutionary computing including routing of telecommunications networks,[13] design of protein sequences,[14] and image-processing tasks such as edge detection, film restoration, face recognition, and Earth-observing satellite multispectral data.[15] Multispectral image analysis and feature extraction coupled to evolutionary computing have been tested on microscopic images from histologic sections of ovarian serous carcinoma [16] and urine cytology specimens with urothelial carcinoma.[17]

The present study describes a method for the interpretation of flow cytometry data applying genetic algorithms.


Flow cytometry data procurement

FCS files were downloaded from dataset #FR-FCM-ZZYA (AML, FlowCAP II), currently maintained in the public website[18] The dataset identifies each patient with a number and the assignment “normal” or “AML.” For each patient, there are eight FCS files, which correspond to acquisitions from eight separate tubes containing specified antibody combinations (tube #1 is an isotype control and #8 is unstained).

Transformation of Flow Cytometry Standard files into Tagged Image File Format (TIFF) file folders

Flow cytometry data contained in FCS files was transformed into TIFF image files and stored in individual folders (one per patient) using R freeware with addition of “prada” library,[19] “tiff” library [20] and the following command script:

>sampdat fdat tiff (filename=“\\Users\\Desktop\\aml_secondbatch\\benign\\temp.tif”, width=553, height=552)

>plot (fdat [, “D”], fdat[, “E”], pch=”.”, xlab=””, ylab=””, log=”y”, axes=NULL)


>imgtemp.tif”, native=TRUE)

>writeTIFF (img, “\\Users\\Desktop\\aml_secondbatch\\benign\\B\\B_C.tif”, compression=c(“none”), reduce=TRUE)


“A” defines the flow cytometry tube in the patient dataset,

“B” is the patient number in the repository,

“C” is an assigned sub index that identifies each TIFF file in the right sequential order,

“D” and “E” selects the flow cytometry channels in the tube.

Each folder contained six two-dimensional TIFF image files in the following sequential order:

TIFF image file #0: CD34-PC5 vs Forward Scatter

TIFF image file #1: CD117-PE vs Forward Scatter

TIFF image file #2: CD45-ECD vs Forward Scatter

TIFF image file #3: CD117-PE vs HLA DR-FITC

TIFF image file #4: CD117-PE vs CD34-PC5

TIFF image file #5: CD20-PC7 vs Forward Scatter.

Transformation of TIFF files into Flexible Image Transport System metafiles

The grayscale TIFF image files contained in each patient folder were stacked together into six-dimensional image cube metafiles where each data plane pixel of x, y location is aligned in a third dimension z. This was achieved by transforming the TIFF image files into one Flexible Image Transport System (FITS) metafile using Interactive Data Language (IDL) 5.6 (Research Systems, Inc., Boulder CO) software. FITS files are a standardized data format widely used in astronomy for the analysis of hyperspectral images.[21] A FITS metafile consists of a sequence of one or more Headers and Data Units. A header is composed of ASCII card images usually read in a string array variable. The header describes the content of the associated data unit, which might be a spectrum, and image or tabular data in ASCII or binary format.


An overview of the process is summarized in [Figure 1]. FITS metafiles were transformed into training files by means of the graphical user interface ALADDIN.[22] ALADDIN allows the user to manually create training files by assigning the “true” or “false” condition to selected areas of the image cube using the region of interest selection tool. The training files were then introduced in the LINUX version of GENIE.[23],[24] Before starting the training process, the evolutionary parameters were set as follows: number of algorithms per generation: 40; maximum number of genes in each algorithm: 20; allowed number of generations: 350; backend classifier: Fisher; crossover mechanism: single point; crossover rate: 0.9; crossover type: standard; elite fraction: 0.1; fitness metric: Hamming; mutation parameter rate: 0.3; mutation rate: 0.6; selection method: Tournament 3; thresholding: intelligent.{Figure 1}

Two separate training sessions were run using four FITS files from acute myeloid leukemia patients (the first four listed in the repository corresponding to patients 5, 7, 9 and 26) and four FITS files from normal patients (the first four listed in the repository corresponding to patients 1, 2, 3, and 4).

In one training session, the right halves of the image cubes from acute myeloid leukemia patients were assigned “true” or “feature” condition, while the right halves of the image cubes from normal patients were selected as “false” or “nonfeature.” A second training session was run using the same four FITS files as the first session, but inverting the selection, meaning that the right halves of the image cubes from acute myeloid leukemia patients were assigned “false” or “nonfeature” condition and the right halves of the image cubes from normal patients were assigned “true” or “feature” condition.


Testing was performed by applying the learned algorithms to FITS metafiles of the testing cohort. The results are expressed in the form of binary image arrays where each pixel is assigned value 1 or “true” and 0 or “false” by the algorithm. The performance of each algorithm can be estimated by observation of the result images. Quantification of the results was also attempted by calculating the number of pixels assigned value 1 by the algorithm or combination of algorithms, using IDL ®.

Statistical analysis

Receiver operator characteristics (ROC) curves were created in Excel Analyze-it software ® (Leeds, UK). Combined sensitivity and specificity were calculated using increasing levels of numerical cutoff value.



The first training session was run to generate an algorithm that identifies the right half portion of the image cubes from acute myeloid leukemia patients as “true.” After 350 iterations, GENIE produced the best algorithm coined “018830” with fitness for the training set of 830.126, where 1000 represents perfect fitness.

The sequence of algorithm 018830 is:

[MEAN rD2 wS1 2 1] [IFLTE rD3 rD4 rD4 rS1 wS2] [ADDP rS2 rD2 wS0] [MEAN rD3 wS2 4 3] [IFLTE rS2 rD0 rD3 rS0 wS1] [QTREG rS1 wS2 wS0 wS1 0.04] [QTREG rD0 wS0 wS3 wS1 0.07] [RANGE rS2 wS0 7 3] [ASF_CLOP rS2 wS1 7 3] [DILATE rS3 wS2 10 6].

Algorithm 018830 is a combination of four neighborhood operators (Mean, Range, Dilate and Alternating Sequential Filter Close/Open), one logical operator (If Less Than Else), one basic mathematical operator (Add Planes) and one region size related statistical operator (QTREG).

Every operation in the sequence appears sequentially listed between brackets. For instance, the first operator MEAN reads data plane 2 (CD45 vs. Forward Scatter) and smooths the data plane with a round (structure element specified by the number 1 at the end of the gene) 2 × 2 kernel (specified by the preceding number 2). The resulting data plane is written in scratch plane S1. Finally, a Fisher Discriminant [25] applies a linear combination of the scratch planes followed by a threshold to produce the binary answer plane.

The second training session was run to generate an algorithm that identifies the right half portion of the image cubes from normal patients as “true.” After 350 iterations, GENIE produced the best algorithm coined “025886” with fitness for the training set regions of 870.188.

The sequence of algorithm 025886 is:

[QTREG rD0 Ws2 wS1 wS0 0.05] [ASF_CLOP Rs2 Ws2 10 4] [ERODE rD1 wS0 4] [ASF_CLOP rS0 wS0 10 0] [OPENCLOSE rS2 wS2 7 0] [SOBELGRAD rD5 wS1] CLOSEOPEN rS1 wS1 9 0].

Algorithm 025886 is a combination of one region size related statistical operator (QTREG) and four neighborhood operators (Alternating Sequential Filter Close/Open, OpenClose, Erode and Sobelgradient).

For a more detailed description, [Supplementary Text 1] lists the IDL code of the operators used by both algorithms.


FITS metafiles obtained from all patients in the repository (except those used in the training session) were used for testing. It consisted 312 normal patients and 39 acute myeloid leukemia patients. The algorithms assign a weighted value from 0 to 255 to every pixel of the GENIE result image, which is then reduced to a binary array by a thresholding parameter. Representative examples of result images obtained after applying algorithms 018330 and 025866 to testing patients are shown in [Figure 2]. Result images from all testing patients using algorithms 018330 and 025866 can be seen in [Supplementary Figures 1 and 2 [SUPPORTING:1]], respectively. Algorithm 018330, applied to FITS metafiles from most acute myeloid leukemia patients, generates binary images with a larger proportion of white (feature) pixels on the right side when compared to normal patients, which show a higher proportion of black (nonfeature) pixels on that area. This is consistent with the fact that algorithm 018330 was trained using the right half of the training FITS metafiles. This was done to facilitate a more coherent algorithm, focused on fewer number or less contradictory features. As expected, algorithm 018330 underperforms on those areas of the FITS metafiles that had never been exposed to, such as the left half and the area of the background that surrounds the flow cytometry plot. On the other hand, algorithm 025866, applied to FITS metafiles from acute myeloid leukemia subjects, results in a larger proportion of black pixels on the right side. Within the IDL ® environment, the left side of the result images was masked and the total number of white pixels used as a measure of category assignment (normal vs. AML). The image results of every subject generated by each algorithm were also combined, to mask those pixels in the array that were classified as “feature” by both 018330 and 025866. The underlying process is exemplified in [Figure 3] for one normal and one AML subject. The numerical results of the entire testing cohort for algorithms 018330 alone, 025866 alone and both algorithms combined can be seen in [Figure 4]a,[Figure 4]b,[Figure 4]c, respectively. When the numerical data are used to differentiate between acute myeloid leukemia and normal patients, algorithm 018330 alone achieves an area under the ROC curve of 0.849 [Figure 5]a, while in algorithm 025866 alone is of 0.842 [Figure 5]b. Both algorithms combined produced an area under the ROC curve of 0.912 [Figure 5]c.{Figure 2}{Figure 3}{Figure 4}{Figure 5}


The present study describes a novel approach in the analysis and interpretation of flow cytometry data using genetic algorithms. Here, the Linux version of GENIE [23] was used to classify flow cytometry data from normal patients and acute myeloid leukemia patients. The learning process follows the classic evolutionary paradigm: a population of candidate image-processing linear algorithms is randomly generated, and the fitness of each individual assessed. After fitness has been assigned, modification of the fittest members of the population follows via selection, crossover and mutation and the step is repeated.[26] Fitness evaluation and reproduction with modification are iterated until some stopping condition is satisfied (for example, a candidate solution reaching a predetermined score is found). The system relies on commercially available IDL ® software for the more computationally intensive fitness evaluation. One advantage of genetic algorithms is that in general, they do not require additional measures to reduce data dimensionality as it happens to other computer learning systems such as support vector machines.[27] The process makes the use of a graphical user interface, which facilitates the hematopathologist-machine interaction, and in this way, specific areas of the multidimensional space could be oriented and/or selected by the operator for training.

Using a small training cohort of eight cases (four normal patients and four acute myeloid leukemia patients), the artificial intelligence system was capable of classifying a cohort of 351 patients (312 normal and 39 acute myeloid leukemia) with an area under the receiver characteristics curve of 0.912.

Although the distinction between these two conditions is not considered a challenging problem for the practicing hematopathologist most of the time, testing it on a less disputable task provides a more suitable introduction of the technique.

The potential impact that the varying technical conditions used by different laboratories may have on the efficiency of a given algorithm is not known. One common limitation of genetic algorithms is their tendency to overfitting, which stresses the importance of a careful selection of training features. Furthermore, the algorithms are dimensionally restricted, which means that the future incorporation of new markers to the panel may need that the system be re-trained. The learning application carries out its classification, not in a context of disease or population identification, but rather spectral/spatial image analysis requiring a way to translate it back for clinical usefulness. Here, the number of pixels classified by the machine as “feature” was intuitively counted to “measure” the results. However, other characteristics in the result planes may prove in the future to be more efficient for each specific task. One should also consider that the image processing operators (or genes) available to the algorithm were originally created for remote-sensing applications. More appropriate mathematical operators can presumably be written in IDL or C, and implemented within this environment.

The cases used here fit only into two categories (AML and normal), when hematopathology practice most commonly involves multi-class decision making. This is a common problem of most artificial intelligence systems, in that they infer binary solutions. Multi-class resolution is usually achieved through decomposition into binary classification steps, in the form of “one versus all (winner takes all)” or one versus one (max wins voting),” and this requires the development of complex hierarchical structures. It is possible that the algorithms described here could misclassify when faced with an unintended tasks. An example would be for algorithm 018330 to classify cases of acute lymphoblastic leukemia as “acute myeloid leukemia present.” This problem could be resolved by generating a second algorithm that differentiates between these two entities.

The original flow cytometry data were obtained running the standard lymphoma/leukemia 24 marker panel which does not include myeloperoxidase. The inclusion of such marker could probably increase the efficiency of the assay, although this needs to be proven. In theory, the system does not intend to identify a population positive for one or more markers (such as CD34 or CD117) but to score a multidimensional composite. For example, based on reading the sequences, algorithm 018830, trained to look for acute myeloid leukemia patients, makes use of all markers in some way (every data plane except D1). Meanwhile algorithm 025886, trained to look for normal subjects, uses data planes with only CD34, CD117, CD20 and forward scatter information only (D0, D1, and D5).

It remains to be addressed what are the capabilities of this technique in the accurate detection of intermediate states such as myelodysplastic syndromes or the assessment of posttreatment minimal residual disease. The incorporation of cell density information in addition to population distribution may be useful in the task. The images generated by the R-Prada platform in this study lack pixel depth (meaning every pixel is 0 or 1). This is because hematopathologists routinely use 1-bit format imagery to interpret the data. However, it is conceivable cell density information in the form of grayscale data could be clinically useful. The common 16-bit image file conveys a dynamic range of 65,535.[28]

Some possible ways to improve the performance of this model are permitted. One option involves retraining a new algorithm with increasing number of training files, perhaps selecting examples containing features that were missed by the preceding algorithm. Acute myeloid leukemia is known to show high variability of antigenic expression depending on lineage and differentiation,[29] which may require the use of more than just one algorithm. As shown in this manuscript, two separate algorithms, trained to perform opposite tasks, were later combined using a simple logical script written in IDL, increasing the accuracy over the testing cohort. This brings up the possibility of developing “cognizant” algorithms capable of classifying over FITS metafiles built from result images of lower-order algorithms, trained on specific features (abstract thinking).

In the recent years, there has been a surge in the development of diverse computational methods applicable to flow cytometry data. A good example of this effort is represented by the “Flow Cytometry: Critical Assessment of Population Identification Methods (FlowCAP) project,” where different methods are compared through specific challenges.[30] One of these challenges, termed FlowCAP-II, involved the identification of cell populations that can discriminate between acute myeloid leukemia positive (n = 43) and healthy donor (n = 316) patients. That same flow cytometry data were used for this study. In the FlowCAP-II challenge, 25 different algorithms were tested, showing F-measures between 0.46 and 1.00. However, it is not known how these would perform under more robust statistical evaluation such as ROC analysis. In the FlowCAP-II study, half of the total data was used for training purposes, whereas in this pilot work, the training cohort represents approximately 2% of the patients.

The flow cytometry data from normal and acute myeloid patients used in this work were obtained through the public web-based This website, provided by The International Society for Advancement of Cytometry, supports the storage, annotation, analysis, and sharing of flow cytometry datasets.[31] The datasets are annotated in compliance with the Minimum Information about Flow Cytometry Experiment (MIFlowCyt) standard, which greatly facilitates third-party interpretation of the data. The dataset used in this study (FR-FCM-ZZYA) has a MIFlowCyt score of 97.12%. Research studies, like the one presented here, reaffirm the notion that sharing flow cytometry data through web-based public repositories allows for the exploration of alternative approaches, perhaps not previously envisioned by the original publisher, and this should be strongly encouraged.


The present work describes a method that applies evolutionary machine learning with genetic algorithms to the interpretation of flow cytometry data. The results from an initial attempt with flow cytometry data from normal and acute myeloid leukemia patients showed great discriminative power and hold great promise.

Financial support and sponsorship


Conflicts of interest

There are no conflicts of interest.


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