Showing results (21-30 of 120) with videos related to

Sort By:
Pageof 12
Human Genetics|February 24, 2005
TLR2 Arg677Trp polymorphism in leprosy: revisitedDheeraj Malhotra, Vineet Relhan, B S N Reddy, et al.
Plos One|October 23, 2008
Computing power and sample size for case-control association studies with copy number polymorphism: application of mixture-based likelihood ratio testWonkuk Kim, Derek Gordon, Jonathan Sebat, et al.
NPJ Schizophrenia|March 18, 2016
Characterization of molecular and cellular phenotypes associated with a heterozygous <i>CNTNAP2</i> deletion using patient-derived hiPSC neural cellsInkyu S Lee, Claudia M B Carvalho, Panagiotis Douvaras, et al.
Life Science Alliance|January 19, 2019
A junction coverage compatibility score to quantify the reliability of transcript abundance estimates and annotation catalogsCharlotte Soneson, Michael I Love, Rob Patro, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 17, 2005
Application of ROMA (representational oligonucleotide microarray analysis) to patients with cytogenetic rearrangementsVaidehi Jobanputra, Jonathan Sebat, Jennifer Troge, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 9, 2004
Distribution of short paired duplications in mammalian genomesElizabeth E Thomas, Nathan Srebro, Jonathan Sebat, et al.
G3 (Bethesda, Md.)|March 3, 2012
Inferring haplotypes of copy number variations from high-throughput data with uncertaintyMamoru Kato, Seungtai Yoon, Naoya Hosono, et al.
Biorxiv : the Preprint Server for Biology|May 7, 2024
Single-nucleus and spatial transcriptomic profiling of human temporal cortex and white matter reveals novel associations with AD pathologyPallavi Gaur, Julien Bryois, Daniela Calini, 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.
Nature Communications|November 22, 2019
Ranking of non-coding pathogenic variants and putative essential regions of the human genomeAlex Wells, David Heckerman, Ali Torkamani, et al.
Pageof 12