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Annual Review of Genomics and Human Genetics|February 15, 2024
RNA Sequencing in Disease DiagnosisCraig Smail, Stephen B MontgomeryAmerican Journal of Human Genetics|July 3, 2021
Nonsense-mediated decay is highly stable across individuals and tissuesNicole A Teran, Daniel C Nachun, Tiffany Eulalio, et al.Cell Genomics|July 8, 2026
Gene dosage differences and non-linear impacts on complex traitsCraig SmailGenome Biology|November 12, 2010
Out of the sequencer and into the wiki as we face new challenges in genome informaticsZemin Ning, Stephen B MontgomeryCold Spring Harbor Molecular Case Studies|December 19, 2018
Diagnosing rare diseases after the exomeLaure Frésard, Stephen B MontgomeryHuman Genetics|July 19, 2019
Identifying causal variants and genes using functional genomics in specialized cell types and contextsBoxiang Liu, Stephen B MontgomeryHuman Heredity|January 12, 2017
Non-Coding Loss-of-Function Variation in Human GenomesZachary Zappala, Stephen B MontgomeryFrontiers in Genetics|June 12, 2013
Detection and impact of rare regulatory variants in human diseaseXin Li, Stephen B MontgomeryPacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|March 14, 2019
SNPs2ChIP: Latent Factors of ChIP-seq to infer functions of non-coding SNPsShankara Anand, Laurynas Kalesinskas, Craig Smail, et al.Cold Spring Harbor Protocols|April 15, 2015
RNA Sequencing and AnalysisKimberly R Kukurba, Stephen B MontgomeryPageof 20