ArticleCytometry. Part A : the journal of the International Society for Analytical Cytology2016
Consistent quantitative gene product expression: #1. Automated identification of regenerating bone marrow cell populations using support vector machines.
Article in Cytometry. Part A : the journal of the International Society for Analytical Cytology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- Trial
- Morphologic remission status is limited compared to ΔN flow cytometry: a Children's Oncology Group AAML0531 report.Blood advances · 2020Trial
- Molecular risk markers define risk of relapse in myeloid leukemia of Down syndrome beyond measurable residual disease.Blood advances · 2026Article
- Application of machine learning in the management of acute myeloid leukemia: current practice and future prospects.Blood advances · 2020Review
- CD33 splicing SNP regulates expression levels of CD33 in normal regenerating monocytes in AML patients.Leukemia & lymphoma · 2018Article
- A 63 signature genes prediction system is effective for glioblastoma prognosis.International journal of molecular medicine · 2018Article
- A 65‑gene signature for prognostic prediction in colon adenocarcinoma.International journal of molecular medicine · 2018Article
- Confirmation of the abnormal lipid metabolism as a risk factor for the disease of leukoaraiosis.Saudi journal of biological sciences · 2017Article
- Consistent quantitative gene product expression: #2. Antigen intensities on bone marrow cells are invariant between individuals.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2016Article
- Consistent quantitative gene product expression: #3. Invariance with age.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2016Article
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Authors and funding
5 authors.
Funding
Abstract
Identification and quantification of maturing hematopoietic cell populations in flow cytometry data sets is a complex and sometimes irreproducible step in data analysis. Supervised machine learning algorithms present promise to automatically classify cells into populations, reducing subjective bias in data analysis. We describe the use of support vector machines (SVMs), a supervised algorithm, to reproducibly identify two distinctly different populations of normal hematopoietic cells, mature lymphocytes and uncommitted progenitor cells, in the challenging setting of pediatric bone marrow specimens obtained 1 month after chemotherapy. Four-color flow cytometry data were collected on a FACS Calibur for 77 randomly selected postchemotherapy pediatric patients enrolled on the Children's Oncology Group clinical trial AAML1031. These patients demonstrated no evidence of detectable residual disease and were divided into training (n = 27) and testing (n = 50) cohorts. SVMs were trained to identify mature lymphocytes and uncommitted progenitor cells in the training cohort before independent evaluation of prediction efficiency in the testing cohort. Both SVMs demonstrated high predictive performance (lymphocyte SVM: sensitivity >0.99, specificity >0.99; uncommitted progenitor cell SVM: sensitivity = 0.94, specificity >0.99) and closely mirrored manual cell classifications by two expert-analysts. SVMs present an efficient, automated methodology for identifying normal cell populations even in stressed bone marrows, replicating the performance of an expert while reducing the intrinsic bias of gating procedures between multiple analysts. © 2016 The Authors. Cytometry Part A published by Wiley Periodicals, Inc. on behalf of ISAC.
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