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WuXi PharmaTech Purchases an Illumina HiSeq X Ten Sequencing System
SAN DIEGO & SHANGHAI–(BUSINESS WIRE)–Mar. 10, 2014– Illumina, Inc. (NASDAQ:ILMN) and WuXi PharmaTech (Cayman) Inc. (NYSE:WX), a leading pharmaceutical, biotechnology, and medical device R&D...
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23andMe CEO: ‘We need to return to delivering health information’
from VentureBeat by Christina Farr AUSTIN, Texas – 23andMe‘s chief executive Anne Wojcicki kicks off her stilettos and sinks into a couch. Minutes into our interview, it’s clear that Wojcicki is...
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exomeSuite: Whole exome sequence variant filtering tool
Exome and whole-genome analyses powered by next-generation sequencing (NGS) have become invaluable tools in identifying causal mutations responsible for Mendelian disorders. Given that individual...
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Comprehensive Molecular Diagnosis of Bardet-Biedl Syndrome by High-Throughput...
Bardet-Biedl syndrome (BBS) is an autosomal recessive disorder with significant genetic heterogeneity. BBS is linked to mutations in 17 genes, which contain more than 200 coding exons. Currently, BBS...
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Agilent Technologies New Target-Enrichment Solutions Address Current...
SANTA CLARA, Calif.–(BUSINESS WIRE)–Agilent Technologies Inc. (NYSE: A) today announced new additions to its market-leading SureSelect target-enrichment product family, which has already enabled...
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Exome sequencing uncovers cause of acute liver failure in young children
Acute liver failure is a rare yet life-threatening disease for young children. It often occurs extremely rapidly, for example, when a child has a fever. Yet in around 50 percent of cases it is unclear...
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Dissecting the diagnostic yield of exome sequencing
Deanna Church – Senior Director of Genomics & Content Technological advances in high throughput, low cost DNA sequencing coupled with the availability of a high quality reference assembly allow us...
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Personal Genome Diagnostics Collaborates on Study Uncovering New Actionable...
Personal Genome Diagnostics Collaborates on Study Uncovering New Actionable Mutations and Prognostic Predictors in Pancreatic Cancer Study in Nature Communications Identifies New Predictors of Patient...
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Can whole-exome sequencing data be used for linkage analysis?
Whole-exome sequencing (WES) has become the strategy of choice to identify causal variants in monogenic disorders. However, the list of candidate variants can be quite large, including false positives...
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VariantPro™ Targeted Sequencing Technology
LC Sciences has developed a customized solution to high-throughput genome wide variant analysis. The VariantPro™ system is comprised of three distinct innovations, all developed by scientists at LC...
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