complex phased variants in inherited retinal disease with long-read sequencing
Published 7 months ago • 296 plays • Length 21:04Download video MP4
Download video MP3
Similar videos
-
18:50
targeted long-read sequencing clarifies complex genetic results and identifies missing variants
-
10:52
the potential clinical utility of amplicon and targeted nanopore sequencing for rare disease
-
21:24
danny e. miller: sequencing resolves complex svs and identifies missing pathogenic variants in u...
-
55:54
empowering comprehensive sequencing at scale
-
11:07
solving genetically undiagnosed inherited neuropathy families: long-read sequencing to the rescue
-
11:40
nanopore sequencing reveals retrotransposon insertions or complex genetic mechanisms rare disorders
-
50:18
streamlining clinical genetic testing: the promise of long-read sequencing
-
11:57
unraveling complex mendelian diseases with nanopore sequencing
-
11:35
nanopore sequencing as a potential diagnostic tool for genetic diseases in the middle east
-
1:42
how nanopore sequencing works
-
9:27
measuring skewed x inactivation by adaptive nanopore sequencing
-
9:34
innovating and improving genome diagnostics using targeted long-read sequencing
-
21:59
population-scale nanopore sequencing to understand the genetics of alzheimer's disease and dementias
-
1:49
nanopore sequencing
-
15:12
human genomics — from targeted to whole-genome sequencing showcase
-
11:29
meow: genome-wide identification of differentially methylated regions using nanopore sequencing data
-
13:26
nanopore sequencing medically relevant dark genomic regions
-
12:04
long-read sequencing for pathogenic and novel variation discovery in rare diseases