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Nature Biotechnology|February 3, 2009
Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencingAndreas Gnirke, Alexandre Melnikov, Jared Maguire, et al.Nature Genetics|July 22, 2011
Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarctionJessica Shea, Vineeta Agarwala, Anthony A Philippakis, et al.Bioinformatics (Oxford, England)|July 31, 2012
zCall: a rare variant caller for array-based genotyping: genetics and population analysisJacqueline I Goldstein, Andrew Crenshaw, Jason Carey, et al.Nature Biotechnology|December 8, 2020
Chromosome-scale, haplotype-resolved assembly of human genomesShilpa Garg, Arkarachai Fungtammasan, Andrew Carroll, et al.Genome Research|February 25, 2010
Integrative analysis of the melanoma transcriptomeMichael F Berger, Joshua Z Levin, Krishna Vijayendran, et al.Plos Genetics|April 18, 2013
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controlsLi Liu, Aniko Sabo, Benjamin M Neale, et al.Plos Genetics|August 10, 2012
The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traitsBenjamin F Voight, Hyun Min Kang, Jun Ding, et al.Nature|April 13, 2012
Patterns and rates of exonic de novo mutations in autism spectrum disordersBenjamin M Neale, Yan Kou, Li Liu, et al.Diabetes|March 26, 2017
A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes RiskAlisa Manning, Heather M Highland, Jessica Gasser, et al.Scientific Data|January 24, 2018
Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controlsJason Flannick, Christian Fuchsberger, Anubha Mahajan, et al.Pageof 2