Appistry has launched the Cancer Genome Analysis Suite, a set of tools for analyzing next-generation sequencing cancer genome data. The suite contains a tool to provide high sensitivity for identifying low-frequency point mutations and difficult to find discrepancies in DNA sequences that are a hallmark of tumor development.

The suite features two of the Broad Institute's tools: the Genome Analysis Toolkit and MuTect for identifying point mutations.

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A new analysis examines the gender gap among paper authors in the sciences and says it may take decades or more to close.

Researchers have uncovered signals of selection that may enable the Bajau people to free five hundreds of feet deep, Reuters reports.

In Science this week: paternally inherited cis-regulatory structural variants in autism, and more.

A new report outlines issues facing the implementation of personalized medicine in the UK, the Independent reports.

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This webinar will review a standardized, high-throughput, and fully automated library prep protocol for human metagenomic analysis.