e08.1 - using genomic resources to interpret the clinical significance of rare variants
Published 2 years ago • 165 plays • Length 30:11Download video MP4
Download video MP3
Similar videos
-
33:49
e08 1 philip beales: functional genomics
-
28:34
e08.1 - do we need to adopt a cautious approach to returning results from genomic research?
-
28:46
e08.2 - towards better interpretation of variants in non-coding regions of the genome
-
49:34
e8.2 heidi rehm: the acmgg recommendations for the interpretation of genetic variants
-
22:02
evaluating the clinical significance of cytogenomic variants
-
51:01
genomic history of indians feat. prof. k thangaraj ep18 full episode #podcast #genetics #research
-
1:00:45
population genetics in an era of genomic health - eimear kenny
-
23:30
overview of gwas theory
-
27:27
e01.2 genome sequencing in newborn screening and rare disease
-
4:19
genomic variants: innocent until proven guilty
-
1:05:57
genetics of personality disorders: the empirical research
-
20:01
panel 2: consistency of interpretation of variants across expert labs/groups, clinvar submissions
-
56:37
human genetics in the next generation: rare variants and common cures
-
48:14
moderated discussion: variant discovery and association - goncalo abecasis
-
15:04
measuring the functional consequences of large numbers of human genetic variants - jay shendure
-
33:25
nhgri's oral history collection: interview with heidi rehm
-
53:35
seminars in genomic medicine: dr daniel macarthur
-
49:28
using human genetics and genomics to unravel causal mechanisms for diabetes
-
3:23
importance of studying rare variants - ashg 2016
-
51:53
translating genome-wide association studies to prevention, diagnostics, and therapeutics
-
37:00
integrating exome variants with other genomic data and functional annotations - david adams
-
54:25
public health impact of rare variants