haplotypes, isoforms, and fusions: towards a richer cancer transcriptome
Published 6 months ago • 336 plays • Length 9:20Download video MP4
Download video MP3
Similar videos
-
9:27
oxford nanopore rna seq enables precise rna isoform discovery & quantification in human brains
-
11:05
potential use of nanopore sequencing in clinical cancer genomics
-
3:27
nanopore sequencing: the most comprehensive insight into cancer genomes
-
4:30
jeffrey rosenfeld│long read sequencing of tumor rna and dna to analyze fusions and amplicons
-
15:04
evaluating and comparing transcriptome sequencing approaches - rachel goldfeder
-
30:50
how to perform tumour-normal nanopore sequencing
-
11:47
a complete analysis of human genomes and transcriptomes using nanopore sequencing
-
55:54
empowering comprehensive sequencing at scale
-
3:04
single-cell analysis with nanopore sequencing
-
26:20
ron ammar | nanopore sequencing for detection of pharmacogenomic variants and haplotypes
-
4:34
characterization of full-length isoforms in single cells with nanopore long-read sequencing - l.tian
-
10:34
eilis hannon: evaluation of nanopore sequencing a comparison with dna methylation microarrays
-
3:43
introduction to nanopore sequencing
-
10:53
investigating structural variations and complex cancer genomes using oxford nanopore sequencing
-
15:12
human genomics — from targeted to whole-genome sequencing showcase
-
41:16
using nanopore sequencing to interrogate the genome, epigenome, and transcriptome
-
8:24
end-to-end human genome nanopore sequencing and analysis
-
47:47
integrating 10x genomics single cell and spatial profiling with oxford nanopore long-read sequen...