New research from Virginia Commonwealth University's School of Pharmacy brings the medical community closer to identifying children with the highest need for treatment and intervention following traumatic events.
Sep 2, 2022
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Researchers at Mayo Clinic's Center for Individualized Medicine have discovered key human genomic signatures that could help explain why COVID-19 is severe in some people and mild in others. After analyzing volumes of diverse ...
Jul 25, 2022
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A new algorithm can predict which genes cause cancer, even if their DNA sequence is not changed. A team of researchers in Berlin combined a wide variety of data, analyzed it with "Artificial Intelligence" and identified numerous ...
Apr 12, 2021
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Life can change dramatically when someone learns they are genetically predisposed to a disease, such as a condition called familial hypercholesterolemia, where a mutated gene can lead to elevated cholesterol and increased ...
Aug 20, 2020
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138
When researchers say they have sequenced the human genome, there is a caveat to this statement: a lot of the human genome is sequenced and assembled, but there are regions that are full of repetitive elements, making them ...
Feb 7, 2019
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New laws are required to control access to medical genetic data by law enforcement agencies, an analysis by University of Queensland researchers has found.
Dec 18, 2018
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Princeton researchers have developed a new computational method that increases the ability to track the spread of cancer cells from one part of the body to another.
Jun 29, 2018
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Extending noninvasive prenatal screening to all 24 human chromosomes can detect genetic disorders that may explain miscarriage and abnormalities during pregnancy, according to a study by researchers at the National Institutes ...
Aug 30, 2017
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A person's DNA sequence can provide a lot of information about how genes are turned on and off, but new research out of Case Western Reserve University School of Medicine suggests the 3-D structure DNA forms as it crams into ...
Sep 20, 2016
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The team behind the Deciphering Developmental Disorders (DDD) Study, one of the world's largest nationwide rare disease genome-wide sequencing initiatives, have developed a novel computational approach to identify genetic ...
Oct 5, 2015
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