long-read sequencing for pathogenic and novel variation discovery in rare diseases
Published 2 months ago • 213 plays • Length 12:04Download video MP4
Download video MP3
Similar videos
-
11:07
solving genetically undiagnosed inherited neuropathy families: long-read sequencing to the rescue
-
11:02
long read sequencing – pacbio and oxford nanopore sequencing explained in 11 minutes
-
15:34
harnessing long-read sequencing for antibiotic discovery - allison guitor
-
55:54
empowering comprehensive sequencing at scale
-
11:04
filling the gap with long-read sequencing: lessons learned from genomics thailand
-
7:54
long read sequencing
-
10:18
long-read sequencing improves detection of non-coding structural variations
-
9:04
exploration of long-read sequencing in the resolution of newborn screening
-
11:35
nanopore sequencing as a potential diagnostic tool for genetic diseases in the middle east
-
15:43
long-read sequencing technologies resolve most dark and camouflaged gene regions | mark ebbert
-
18:50
targeted long-read sequencing clarifies complex genetic results and identifies missing variants
-
9:34
innovating and improving genome diagnostics using targeted long-read sequencing
-
4:27
using long-read sequencing to generate a case specific reference genome for pathogen strain typing
-
29:10
dr blake hanson | applications of long-read sequencing in infectious disease genomics
-
11:40
nanopore sequencing reveals retrotransposon insertions or complex genetic mechanisms rare disorders
-
22:44
andre reis: a long-read nanopore sequencing platform for indigenous genomics