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Gigascience|April 8, 2026
NEXT-scASV: A Nextflow Pipeline for Allele-Specific Variants Calling from single cell RNA-seq dataAndrey Shevtsov, Andrey Buyan, Vladimir Nozdrin, et al.
Nature Communications|February 18, 2025
Statistical framework for calling allelic imbalance in high-throughput sequencing dataAndrey Buyan, Georgy Meshcheryakov, Viacheslav Safronov, et al.
Nature Communications|April 17, 2026
Rare regulatory mutations disrupt mesenchymal molecular programs driving endocardial cushion formation in bicuspid aortic valveArtemy Zhigulev, Andrey Buyan, Enikő Lázár, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2024
Perspectives on Codebook: sequence specificity of uncharacterized human transcription factorsArttu Jolma, Kaitlin U Laverty, Ali Fathi, et al.
Biorxiv : the Preprint Server for Biology|December 3, 2025
Inferring binding specificities of human transcription factors with the wisdom of crowdsNikita Gryzunov, Dmitry Penzar, Vasilii Kamenets, et al.
Communications Biology|November 7, 2025
Cross-platform motif discovery and benchmarking to explore binding specificities of poorly studied human transcription factorsIlya E Vorontsov, Ivan Kozin, Sergey Abramov, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2024
Cross-platform DNA motif discovery and benchmarking to explore binding specificities of poorly studied human transcription factorsIlya E Vorontsov, Ivan Kozin, Sergey Abramov, et al.
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