Driving Genomics Forward with DNBSEQ Technology
Rade Drmanac, Ph.D.
Monday, October 14, 2024
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Chapters
Introduction
Complete Genomics
Technology Proven on Multiple Applications with 6000+ Publications
Powering the Complete NGS Workflow
DNBSEQ Sequencing Product Portfolio
DNBSEQ™ Technology
DNBSEQ™ Technology: Make DNB
DNBSEQ – Sub $100 Genome is Here
Enabling Even More Efficient DNBSEQ: Toward the $10 genome
DNBSEQ powered the start of WGS
WGS-NA12878 Genome Accuracy
Exceptional WGS accuracy on GIAB v4.2.1 benchmark samples
Complete Genomics WGS Medically Relevant Gene Performance - HG002/NA24385
CompleteWGS as a new WGS standard
What are co-barcoded reads generated by stLFR?
Two key advantages of stLFR
Importance of haplotype phasing
Phasing separates somatic mutations (or errors) from inherited heterozygotes in WGS
CompleteWGS metrics
HG002 Phased contigs
Genes with compound heterozygous SNPs
High Coverage in Difficult Regions
Reducing genomic “blind zones”
Variant Calling in Blind Zones
Variant Calling in Blind Zones
Our Partners
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