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Frontiers in Immunology|July 6, 2016
Genetic Diagnosis Using Whole Exome Sequencing in Common Variable ImmunodeficiencyPatrick Maffucci, Charles A Filion, Bertrand Boisson, et al.
Nucleic Acids Research|May 3, 2019
SeqTailor: a user-friendly webserver for the extraction of DNA or protein sequences from next-generation sequencing dataPeng Zhang, Bertrand Boisson, Peter D Stenson, et al.
Genome Medicine|May 14, 2024
The landscape of rare genetic variation associated with inflammatory bowel disease and Parkinson's disease comorbidityMeltem Ece Kars, Yiming Wu, Peter D Stenson, et al.
American Journal of Human Genetics|January 11, 2016
Genomic Signatures of Selective Pressures and Introgression from Archaic Hominins at Human Innate Immunity GenesMatthieu Deschamps, Guillaume Laval, Maud Fagny, et al.
Bioinformatics (Oxford, England)|December 12, 2018
PopViz: a webserver for visualizing minor allele frequencies and damage prediction scores of human genetic variationsPeng Zhang, Benedetta Bigio, Franck Rapaport, et al.
Research Square|November 19, 2025
Prediction of human missense variant effects from functional evidenceBarış Kayaalp, Kerem Çil, Clément Conil, et al.
Methods in Molecular Biology (Clifton, N.J.)|February 7, 2019
Biclustering Analysis of Co-regulation Patterns in Nuclear-Encoded Mitochondrial Genes and Metabolic PathwaysRobert B Bentham, Kevin Bryson, Gyorgy Szabadkai
Current Protein & Peptide Science|April 14, 2007
Computer-assisted protein domain boundary prediction using the DomPred serverKevin Bryson, Domenico Cozzetto, David T Jones
Nucleic Acids Research|September 16, 2017
MCbiclust: a novel algorithm to discover large-scale functionally related gene sets from massive transcriptomics data collectionsRobert B Bentham, Kevin Bryson, Gyorgy Szabadkai
Bioinformatics Advances|June 25, 2026
GDIv2: improving variant selection from human exomesEstelle Talouarn, Yoann Seeleuthner, Astrid Marchal, et al.
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