{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,29]],"date-time":"2026-03-29T00:43:29Z","timestamp":1774745009943,"version":"3.50.1"},"reference-count":71,"publisher":"Oxford University Press (OUP)","issue":"2","license":[{"start":{"date-parts":[[2026,2,2]],"date-time":"2026-02-02T00:00:00Z","timestamp":1769990400000},"content-version":"vor","delay-in-days":1,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"name":"American Association for Cancer Research and Breast Cancer Research Foundation"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2026,2,3]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Motivation<\/jats:title>\n                    <jats:p>Differential expression and marker gene selection methods for single-cell RNA-sequencing (scRNA-seq) data can struggle to identify small sets of informative genes, especially for subtle differences between cell states, as can be induced by disease or treatment.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>We present iterative logistic regression (iLR) for the identification of small sets of informative marker genes. iLR applied logistic regression iteratively with a Pareto front optimization to balance gene set size with classification performance. Benchmarking iLR on in silico datasets, we demonstrated its comparable performance to the state-of-the-art at single-cell classification using only a fraction of the genes. We then tested iLR on its ability to distinguish neuronal cell subtypes in healthy versus autism spectrum disorder patients and find that it achieves high accuracy with small sets of disease-relevant genes. Applying iLR to investigate immunotherapeutic effects in cell types from different tumor microenvironments, we found that iLR infers informative genes that translate across organs and even species (mouse-to-human) comparison. We predicted via iLR that entinostat acts in part through the modulation of myeloid cell differentiation routes in the lung microenvironment. Overall, iLR provides means to infer interpretable transcriptional signatures from complex datasets with prognostic or therapeutic potential.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Availability and implementation<\/jats:title>\n                    <jats:p>iLR is freely available at GitHub https:\/\/github.com\/maclean-lab\/iLR and Zenodo https:\/\/zenodo.org\/records\/17728797.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1093\/bioinformatics\/btag051","type":"journal-article","created":{"date-parts":[[2026,1,28]],"date-time":"2026-01-28T12:44:21Z","timestamp":1769604261000},"source":"Crossref","is-referenced-by-count":1,"title":["Inference of marker genes of subtle cell state changes via iLR: iterative logistic regression"],"prefix":"10.1093","volume":"42","author":[{"given":"Yingtong","family":"Liu","sequence":"first","affiliation":[{"name":"Department of Quantitative and Computational Biology, Dornsife College of Letters, Arts and Sciences, University of Southern California , Los Angeles, CA 90089,","place":["United States"]}]},{"given":"Aaron G","family":"Baugh","sequence":"additional","affiliation":[{"name":"Division of Medical Oncology, Department of Medicine, Keck School of Medicine, Norris Comprehensive Cancer Center, University of Southern California , Los Angeles, CA 90033,","place":["United States"]}]},{"given":"Evanthia T","family":"Roussos Torres","sequence":"additional","affiliation":[{"name":"Division of Medical Oncology, Department of Medicine, Keck School of Medicine, Norris Comprehensive Cancer Center, University of Southern California , Los Angeles, CA 90033,","place":["United States"]}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-0689-7907","authenticated-orcid":false,"given":"Adam L","family":"MacLean","sequence":"additional","affiliation":[{"name":"Department of Quantitative and Computational Biology, Dornsife College of Letters, Arts and Sciences, University of Southern California , Los Angeles, CA 90089,","place":["United States"]}]}],"member":"286","published-online":{"date-parts":[[2026,2,2]]},"reference":[{"key":"2026022206565102400_btag051-B1","doi-asserted-by":"crossref","first-page":"36","DOI":"10.1186\/2040-2392-4-36","article-title":"SFARI gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)","volume":"4","author":"Abrahams","year":"2013","journal-title":"Mol Autism"},{"key":"2026022206565102400_btag051-B2","doi-asserted-by":"crossref","first-page":"11345","DOI":"10.18632\/oncotarget.2489","article-title":"Interactome analysis of myeloid-derived suppressor cells in murine models of colon and breast cancer","volume":"5","author":"Aliper","year":"2014","journal-title":"Oncotarget"},{"key":"2026022206565102400_btag051-B3","doi-asserted-by":"crossref","first-page":"R106","DOI":"10.1186\/gb-2010-11-10-r106","article-title":"Differential expression analysis for sequence count 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