A method for finding genes that spur tumor growth takes advantage of machine learning algorithms to sift through reams of molecular data collected from studies of cancer cell lines, mouse models and human patients.
Jan 21, 2020
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A new liquid biopsy test could detect microsatellite instability (MSI) and tumor mutational burden (TMB), indicating that it could help determine which patients are likely to respond to immune checkpoint inhibitors, according ...
Sep 11, 2019
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A genomic strategy implemented by researchers at Baylor College of Medicine can efficiently increase the molecular diagnostic rate of undiagnosed diseases. The researchers report in the New England Journal of Medicine that ...
Jun 20, 2019
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The Democratic Republic of Congo is battling an Ebola outbreak. As is the case with any disease caused by pathogenic viruses – like Zika or influenza – Ebola spreads dangerously and unpredictably. This makes tracking ...
Jan 14, 2019
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The National Institute on Aging Genetics of Alzheimer's Disease Data Storage Site (NIAGADS) will begin making large-scale DNA sequence data available to investigators. The goal is to make Alzheimer's disease-relevant genetic ...
Jul 23, 2018
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A Delaware team including Erin Crowgey, Ph.D., associate director of Bioinformatics with Nemours Biomedical Research, has published a study in the peer-reviewed journal BMC Bioinformatics, showing that DNA patterns in circulating ...
Jun 22, 2018
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Statistics Canada recently released its 2016 census data, which depicts a Canada that is more diverse than ever before. Today, nearly a quarter of Canadians belong to a "visible minority" and 1.7 million Canadians are Indigenous.
Nov 14, 2017
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I had my complete genome sequenced a few years ago – all six billion base pairs of it. And rather than keeping it to myself, I became the first person in the world to make it publicly available by donating it to the Personal ...
Sep 13, 2017
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AnneMarie Ciccarella, a fast-talking 57-year-old brunette with a more than a hint of a New York accent, thought she knew a lot about breast cancer. Her mother was diagnosed with the disease in 1987, and several other female ...
Jul 18, 2017
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Uncovering rare susceptibility variants that contribute to the causes of complex diseases requires large sample sizes and massively parallel sequencing technologies. These sample sizes, often made up of exome and genome data ...
Jun 30, 2017
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