data to discovery: tools to identify pathogenic structural variants in patients with genetic disease
Published 4 years ago • 493 plays • Length 44:04Download video MP4
Download video MP3
Similar videos
-
59:14
insights: identification of candidate variants using exome data in ophthalmic genetics
-
33:51
reliable nucleotide, indel, and structural variant detection in diverse populations
-
3:46
pediatric cancer genome project: 10 years of discovery
-
33:38
structural variants - jan korbel
-
51:10
from genetic risk variant discovery to functional validation in autoimmune diseases
-
2:37
#meetthespeaker - genomic data for drug discovery with keren carss
-
29:59
the need for criteria to implicate dna variants: real-world examples - mark daly
-
13:36
variant bio aws: from remote villages to new therapies through cloud-based genomics
-
32:28
genomic landscapes: leveraging genetic evidence throughout the pharma pipeline
-
6:08
how can genomic and health data shared by patients inform variant classification?
-
23:18
clinical gene discovery - katherine rauen
-
43:44
webinar series: discovering genetic variants to unlock treatment solutions
-
7:27
an artificial intelligence method for fast diagnosis of rare genetic disease
-
2:13
new tool for finding variants in sanger sequencing | eshg 2015
-
16:48
maze therapeutics aws: a human genetics platform for drug discovery and development
-
28:25
interpreting variants in non-coding regions of the genome - lisa brooks
-
23:17
decipher – ejp rd webinar (27 may 2021)
-
40:49
rare variants and drug target discovery
-
21:34
needles in a stack of needles scouring dna variants for rare genetic disease culprit #wiser2022