Showing results (41-50 of 107) with videos related to

Sort By:
Pageof 11
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