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NAR Genomics and Bioinformatics|August 23, 2023
BioConvert: a comprehensive format converter for life sciencesHugo Caro, Sulyvan Dollin, Anne Biton, et al.NAR Genomics and Bioinformatics|August 28, 2023
Prediction of G4 formation in live cells with epigenetic data: a deep learning approachAnna Korsakova, Anh Tuân PhanNAR Genomics and Bioinformatics|October 18, 2023
TAGADA: a scalable pipeline to improve genome annotations with RNA-seq dataCyril Kurylo, Cervin Guyomar, Sylvain Foissac, et al.NAR Genomics and Bioinformatics|July 14, 2023
Transmorph: a unifying computational framework for modular single-cell RNA-seq data integrationAziz Fouché, Loïc Chadoutaud, Olivier Delattre, et al.NAR Genomics and Bioinformatics|July 14, 2023
A low-coverage 3' RNA-seq to detect homeolog expression in polyploid wheatJianqiang Sun, Moeko Okada, Toshiaki Tameshige, et al.NAR Genomics and Bioinformatics|June 30, 2023
ViCloD, an interactive web tool for visualizing B cell repertoires and analyzing intraclonal diversities: application to human B-cell tumorsLucile Jeusset, Nika Abdollahi, Thibaud Verny, et al.NAR Genomics and Bioinformatics|June 19, 2023
scROSHI: robust supervised hierarchical identification of single cellsMichael Prummer, Anne Bertolini, Lars Bosshard, et al.NAR Genomics and Bioinformatics|June 9, 2021
Known sequence features can explain half of all human gene endsAleksei Shkurin, Timothy R HughesNAR Genomics and Bioinformatics|May 28, 2021
Assessing the functional relevance of splice isoformsFernando Pozo, Laura Martinez-Gomez, Thomas A Walsh, et al.NAR Genomics and Bioinformatics|November 3, 2021
Ideafix: a decision tree-based method for the refinement of variants in FFPE DNA sequencing dataMaitena Tellaetxe-Abete, Borja Calvo, Charles LawriePageof 102