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NAR Genomics and Bioinformatics|April 18, 2024
A method to comprehensively identify germline SNVs, INDELs and CNVs from whole exome sequencing data of BRCA1/2 negative breast cancer patientsAndrea Bianchi, Veronica Zelli, Andrea D'Angelo, et al.
NAR Genomics and Bioinformatics|April 18, 2024
Spinach genomes reveal migration history and candidate genes for important crop traitsAn Nguyen-Hoang, Felix L Sandell, Heinz Himmelbauer, et al.
NAR Genomics and Bioinformatics|April 26, 2024
Scalable and efficient DNA sequencing analysis on different compute infrastructures aiding variant discoveryFriederike Hanssen, Maxime U Garcia, Lasse Folkersen, et al.
NAR Genomics and Bioinformatics|December 14, 2023
A Bayesian noisy logic model for inference of transcription factor activity from single cell and bulk transcriptomic dataArgenis Arriojas, Susan Patalano, Jill Macoska, et al.
NAR Genomics and Bioinformatics|January 8, 2024
Investigation of the usefulness of liver-specific deconvolution method by establishing a liver benchmark datasetIori Azuma, Tadahaya Mizuno, Katsuhisa Morita, et al.
NAR Genomics and Bioinformatics|June 26, 2026
Challenges in predicting chromatin accessibility differences between speciesAmy Z M Stephen, Arian Raje, Heather H Sestili, et al.
NAR Genomics and Bioinformatics|June 26, 2026
Power-law penalties correct distance bias in single-cell co-accessibility and deep-learning chromatin interaction predictionsLuca Schlegel, Fabio Gómez Cano, Alexandre P Marand, et al.
NAR Genomics and Bioinformatics|July 6, 2026
Correction to 'SyMetrics: an integrated machine learning model for evaluating the pathogenicity of synonymous variants in the human genome'
NAR Genomics and Bioinformatics|July 17, 2026
The challenges of single cell transcriptomics on difficult human tissue: the placentaTheodoros Xenakis, George T Hall, Jose J Moreno-Villena, et al.
NAR Genomics and Bioinformatics|August 6, 2026
Unveiling the terra cognita of sequence spaces using Cartesian projection of asymmetric distancesAlban Ramette
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