This article was originally published on May 25.

Fluidigm said today that the Broad Institute has purchased an Access Array system to automate sample prep for targeted resequencing.

Access Array enhances the capabilities of next-generation sequencing platforms by allowing the preparation of several sample libraries in parallel, Fluidigm said. The multiplexed system enables parallel amplification of 48 samples — the equivalent of 48 sequencing libraries — in a few hours, according to the company.

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US News & World Report writes that genetic testing of lung tumors can help identify treatments for patients.

A team of researchers plans to sample Loch Ness for environmental DNA, according to Newsweek.

The New York Times writes about the appearance of mosaicism in healthy people.

In PNAS this week: insecticide resistance patterns Anopheles gambiae mosquito, transcriptome patterns in Pseudomonas aeruginosa during infection, and more.

Jun
19
Sponsored by
ACD

This webinar will provide evidence for the use of RNA in situ hybridization (RNA ISH) as a replacement for immunohistochemistry (IHC) in cancer research and diagnostic applications.

Jun
21
Sponsored by
Roche

This webinar will provide a detailed look at how a genomics lab implemented next-generation sequencing (NGS) liquid biopsy assays into its in-house clinical research program.