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Human Genetics|July 19, 2019
Identifying causal variants and genes using functional genomics in specialized cell types and contextsBoxiang Liu, Stephen B MontgomeryJournal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|April 1, 2018
Recurrently Mutated Genes Differ between Leptomeningeal and Solid Lung Cancer Brain MetastasesYingmei Li, Boxiang Liu, Ian David Connolly, et al.Genome 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 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 MontgomeryAnnual Review of Genomics and Human Genetics|February 15, 2024
RNA Sequencing in Disease DiagnosisCraig Smail, Stephen B MontgomeryBMC Medical Informatics and Decision Making|September 7, 2021
ParaMed: a parallel corpus for English-Chinese translation in the biomedical domainBoxiang Liu, Liang HuangFrontiers in Artificial Intelligence|January 6, 2022
Acronyms and Opportunities for Improving Deep NetsKenneth Church, Boxiang LiuCold Spring Harbor Protocols|April 15, 2015
RNA Sequencing and AnalysisKimberly R Kukurba, Stephen B MontgomeryPageof 22