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NAR Genomics and Bioinformatics|December 22, 2025
A practical framework for predicting splicing single nucleotide variants in exome sequencingYasuhiro Utsuno, Kohei Hamanaka, Masamune Sakamoto, et al.NAR Genomics and Bioinformatics|December 12, 2025
Genome sequence assembly and annotation of MATA and MATB strains of Yarrowia lipolyticaNarges Zali, Osama El Demerdash, Kapeel Chougule, et al.NAR Genomics and Bioinformatics|December 12, 2025
HaploExplore, a software specifically designed for the detection of minor allele (MiA-) haploblocksMatilde Manetti, Samuel Hiet, Myriam Rahmouni, et al.NAR Genomics and Bioinformatics|December 12, 2025
Genomic data representations for horizontal gene transfer detectionAndre Jatmiko Wijaya, Aleksandar Anžel, Hugues Richard, et al.NAR Genomics and Bioinformatics|November 3, 2025
Single-cell aneuploidy and chromosomal arm imbalances define subclones with divergent transcriptomic phenotypesXiangqi Bai, Billy T Lau, Anuja Sathe, et al.NAR Genomics and Bioinformatics|July 14, 2025
Signal peptides restrict genome evolution and A-to-I RNA editingYuange Duan, Shuxian Chen, Wanzhi Cai, et al.NAR Genomics and Bioinformatics|July 14, 2025
PyOrthoANI, PyFastANI, and Pyskani: a suite of Python libraries for computation of average nucleotide identityMartin Larralde, Georg Zeller, Laura M CarrollNAR Genomics and Bioinformatics|June 30, 2025
Charm is a flexible pipeline to simulate chromosomal rearrangements on Hi-C-like dataMiroslav Nuriddinov, Polina Belokopytova, Veniamin FishmanNAR Genomics and Bioinformatics|May 14, 2025
Correction to 'ChEC-seq2: an improved chromatin endogenous cleavage sequencing method and bioinformatic analysis pipeline for mapping in vivo protein-DNA interactions'NAR Genomics and Bioinformatics|May 15, 2025
Experience in developing the human genome standard E701Iuliia Vasiliadis, Vera Belova, Anna Shmitko, et al.Pageof 102