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American Journal of Human Genetics|May 18, 2010
Pooled association tests for rare variants in exon-resequencing studiesAlkes L Price, Gregory V Kryukov, Paul I W de Bakker, et al.Nature|August 29, 2014
Cobalt-56 γ-ray emission lines from the type Ia supernova 2014JE Churazov, R Sunyaev, J Isern, et al.Nature Genetics|February 5, 2020
Identification of cancer driver genes based on nucleotide contextFelix Dietlein, Donate Weghorn, Amaro Taylor-Weiner, et al.Nature Genetics|February 21, 2017
Limited statistical evidence for shared genetic effects of eQTLs and autoimmune-disease-associated loci in three major immune-cell typesSung Chun, Alexandra Casparino, Nikolaos A Patsopoulos, et al.Nature|February 20, 2015
Cell-of-origin chromatin organization shapes the mutational landscape of cancerPaz Polak, Rosa Karlić, Amnon Koren, et al.Nature Genetics|January 26, 2016
Genes with monoallelic expression contribute disproportionately to genetic diversity in humansVirginia Savova, Sung Chun, Mashaal Sohail, et al.Bioinformatics Advances|October 10, 2024
FAVOR-GPT: a generative natural language interface to whole genome variant functional annotationsThomas Cheng Li, Hufeng Zhou, Vineet Verma, et al.Proceedings of the National Academy of Sciences of the United States of America|January 21, 2014
Searching for missing heritability: designing rare variant association studiesOr Zuk, Stephen F Schaffner, Kaitlin Samocha, et al.Medrxiv : the Preprint Server for Health Sciences|December 25, 2025
Learning Patient Similarity from Genomics for Precision OncologyMaha Shady, Brendan Reardon, Sharon Jiang, et al.Science (New York, N.Y.)|April 7, 2022
Genome-wide analysis of somatic noncoding mutation patterns in cancerFelix Dietlein, Alex B Wang, Christian Fagre, et al.Pageof 11