CHICAGO (GenomeWeb) – Genome informatics vendor DNAnexus and variant analysis software company Saphetor are integrating their technologies in hopes of creating a seamless platform for genome-based biomarker discovery and interpretation.

Users can now access Saphetor's technology to annotate and classify variants from next-generation sequencing directly from the DNAnexus cloud platform, the two companies said. Saphetor performs whole-genome analysis by running NGS results through a database of 33 billion variant annotation points.

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Thermo Fisher Scientific says it will no longer sell machines in China's Xinjiang region, according to the Wall Street Journal.

The University of Zurich's Ruedi Aebersold and his colleagues analyzed a dozen HeLa cell lines to find differences in gene expression, protein levels, and more.

New Scientist reports that 20 percent of human and yeast proteins are uncharacterized.

In Nature this week: protein-coding variants associated with body-fat distribution, and more.

Mar
14
Sponsored by
BD

In this webinar, Dr. Wendy Béguelin of Weill Cornell Medicine will discuss how she used the BD Rhapsody single-cell RNA-seq platform and YFP floxed reporter mouse models to study how lymphoma-associated mutations disrupt the immune system by affecting GC B-cell states, explaining the biology of initiation of low-grade follicular lymphoma.

Apr
09
Sponsored by
Sophia Genetics

This webinar will present the utility of a personalized in silico analytical approach for the routine clinical diagnosis of channelopathies and cardiomyopathies.