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Biorxiv : the Preprint Server for Biology|July 9, 2024
Variant Impact Predictor database (VIPdb), version 2: Trends from 25 years of genetic variant impact predictorsYu-Jen Lin, Arul S Menon, Zhiqiang Hu, et al.Genome Medicine|July 13, 2023
ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burdenAndrew G Sharo, Yangyun Zou, Aashish N Adhikari, et al.Journal of Structural Biology|January 27, 2009
A method for the alignment of heterogeneous macromolecules from electron microscopyMaxim Shatsky, Richard J Hall, Steven E Brenner, et al.Genome Research|July 3, 2014
Comparison of D. melanogaster and C. elegans developmental stages, tissues, and cells by modENCODE RNA-seq dataJingyi Jessica Li, Haiyan Huang, Peter J Bickel, et al.Human Genomics|August 28, 2024
Variant Impact Predictor database (VIPdb), version 2: trends from three decades of genetic variant impact predictorsYu-Jen Lin, Arul S Menon, Zhiqiang Hu, et al.Nature Neuroscience|May 12, 2009
Sparse temporal coding of elementary tactile features during active whisker sensationShantanu P Jadhav, Jason Wolfe, Daniel E FeldmanPlos Computational Biology|November 9, 2018
Putting benchmarks in their rightful place: The heart of computational biologyBjoern Peters, Steven E Brenner, Edwin Wang, et al.Genome Research|July 26, 2011
Genome-scale phylogenetic function annotation of large and diverse protein familiesBarbara E Engelhardt, Michael I Jordan, John R Srouji, et al.Journal of Structural Biology|January 21, 2010
Automated multi-model reconstruction from single-particle electron microscopy dataMaxim Shatsky, Richard J Hall, Eva Nogales, et al.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|January 17, 2015
Personalized medicine: from genotypes, molecular phenotypes and the quantified self, towards improved medicineJoel T Dudley, Jennifer Listgarten, Oliver Stegle, et al.Pageof 19