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NAR Genomics and Bioinformatics|April 11, 2022
nMOWChIP-seq: low-input genome-wide mapping of non-histone targetsZhengzhi Liu, Lynette B Naler, Yan Zhu, et al.NAR Genomics and Bioinformatics|July 20, 2022
Benchmarking computational methods for B-cell receptor reconstruction from single-cell RNA-seq dataTommaso Andreani, Linda M Slot, Samuel Gabillard, et al.NAR Genomics and Bioinformatics|March 10, 2022
Generation and network analysis of an RNA-seq transcriptional atlas for the ratKim M Summers, Stephen J Bush, Chunlei Wu, et al.NAR Genomics and Bioinformatics|March 10, 2022
OMARU: a robust and multifaceted pipeline for metagenome-wide association studyToshihiro Kishikawa, Yoshihiko Tomofuji, Hidenori Inohara, et al.NAR Genomics and Bioinformatics|November 29, 2023
Phased secondary small interfering RNAs in Camellia sinensis var. assamicaAngbaji Suo, Jun Yang, Chunyi Mao, et al.NAR Genomics and Bioinformatics|September 14, 2023
Identification of experimentally-supported poly(A) sites in single-cell RNA-seq data with SCINPASYoungbin Moon, Dominik Burri, Mihaela ZavolanNAR Genomics and Bioinformatics|September 14, 2023
Alternative splicing impacts microRNA regulation within coding regionsLena Maria Hackl, Amit Fenn, Zakaria Louadi, et al.NAR Genomics and Bioinformatics|September 14, 2023
MetaTransformer: deep metagenomic sequencing read classification using self-attention modelsAlexander Wichmann, Etienne Buschong, André Müller, et al.NAR Genomics and Bioinformatics|September 8, 2023
SUPREME: multiomics data integration using graph convolutional networksZiynet Nesibe Kesimoglu, Serdar BozdagNAR Genomics and Bioinformatics|October 24, 2023
Retraction of 'known sequence features can explain half of all human gene ends'Pageof 99