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The software combines the output of multiple data projection methods with gene signature information to help users identify meaningful biological processes.
The partners will evaluate various established research solutions including a number of variant calling methods for potential clinical use.
PNRI researchers will be able to analyze information from over 600,000 discrete tumor, blood, and urine samples from around 25,000 patients.
Sentieon's first products re-implement the Broad's GATK and MuTect but offer 10-fold, and in some cases 20- to 50-fold, increases in processing speed.
The study found that combining whole-genome expression or genome-wide methylation data with clinical data improves survival predictions in breast cancer cases.
A key feature of the platform is iMethods, which lets users pack their analysis tools and protocols in Docker containers and share them as part of their papers.
TheSTARPlatform includes tools for analyzing genomic data from raw sequence through to variants calls as well as for compressing and storing data.
The laboratory will employ dedicated computational biologists and bioinformaticians to analyze genomic datasets for ALSF-funded researchers and other scientists.
Recent numbers from the PMKB website show that the repository currently contains 144 genes, 458 variant descriptions, and 286 clinical interpretations.
The new center will focus on supporting and mentoring junior faculty researchers as well as on building bioinformatics infrastructure for projects.
The Washington Post reports on researchers' efforts to determine the effect of an increasingly common SARS-CoV-2 mutation.
Florida Politics reports Florida's law barring life, long-term care, and disability insurers from using genetic information in coverage decisions went into effect at the beginning of July.
A new analysis finds a link between popular media coverage of a scientific study and how often that paper is cited.
In Nature this week: CRISPR approaches to editing plant genomes, way to speed up DNA-PAINT, and more.