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American Journal of Human Genetics|October 24, 2007
Common single-nucleotide polymorphisms act in concert to affect plasma levels of high-density lipoprotein cholesterolVictor Spirin, Steffen Schmidt, Alexander Pertsemlidis, et al.American Journal of Human Genetics|January 9, 2008
Shifting paradigm of association studies: value of rare single-nucleotide polymorphismsIvan P Gorlov, Olga Y Gorlova, Shamil R Sunyaev, et al.Proceedings of the National Academy of Sciences of the United States of America|February 8, 2013
Impact of deleterious passenger mutations on cancer progressionChristopher D McFarland, Kirill S Korolev, Gregory V Kryukov, et al.Nature Communications|June 8, 2021
Replicate sequencing libraries are important for quantification of allelic imbalanceAsia Mendelevich, Svetlana Vinogradova, Saumya Gupta, et al.Protein Engineering|June 9, 1999
PSIC: profile extraction from sequence alignments with position-specific counts of independent observationsS R Sunyaev, F Eisenhaber, I V Rodchenkov, et al.Nature Genetics|March 17, 2009
Human mutation rate associated with DNA replication timingJohn A Stamatoyannopoulos, Ivan Adzhubei, Robert E Thurman, et al.Genome Research|May 8, 2021
Purifying selection on noncoding deletions of human regulatory loci detected using their cellular pleiotropyDavid W Radke, Jae Hoon Sul, Daniel J Balick, et al.Genome Biology|October 26, 2018
PINES: phenotype-informed tissue weighting improves prediction of pathogenic noncoding variantsCorneliu A Bodea, Adele A Mitchell, Alex Bloemendal, et al.Biorxiv : the Preprint Server for Biology|November 19, 2025
Segregating DNA lesions point to high selective advantage of tumor initiating cellsVladimir Seplyarskiy, Maha Shady, Maria A Andrianova, et al.American Journal of Human Genetics|November 27, 2012
Differential relationship of DNA replication timing to different forms of human mutation and variationAmnon Koren, Paz Polak, James Nemesh, et al.Pageof 11