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Bioinformatics (Oxford, England)|June 1, 2011
SVA: software for annotating and visualizing sequenced human genomesDongliang Ge, Elizabeth K Ruzzo, Kevin V Shianna, et al.American Journal of Human Genetics|September 4, 2012
Using ERDS to infer copy-number variants in high-coverage genomesMingfu Zhu, Anna C Need, Yujun Han, et al.Plos Genetics|June 26, 2010
Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease geneNara L M Sobreira, Elizabeth T Cirulli, Dimitrios Avramopoulos, et al.Human Molecular Genetics|September 8, 2009
A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTABAnna C Need, Deborah K Attix, Jill M McEvoy, et al.American Journal of Human Genetics|August 7, 2012
Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophreniaAnna C Need, Joseph P McEvoy, Massimo Gennarelli, et al.Plos Genetics|September 15, 2010
The characterization of twenty sequenced human genomesKimberly Pelak, Kevin V Shianna, Dongliang Ge, et al.American Journal of Human Genetics|August 7, 2012
Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsyErin L Heinzen, Chantal Depondt, Gianpiero L Cavalleri, et al.American Journal of Human Genetics|April 20, 2010
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromesErin L Heinzen, Rodney A Radtke, Thomas J Urban, et al.Pageof 2