Mutations discovered in the first Brazilian case of coronavirus are no cause for alarm, a leading virologist says, as the virus seems to be remaining stable enough for a single vaccine to work.
Mar 5, 2020
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Treating physicians need information about the molecular subtype of the tumor if they are to provide targeted therapy for colorectal carcinoma. A research team from University Hospital Zurich and the University of Oxford ...
Jul 5, 2019
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St. Jude Children's Research Hospital has re-defined the gold standard for diagnostic testing of childhood cancer patients in the precision-medicine era and has implemented the testing for new cancer patients. The findings ...
Oct 12, 2018
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A team of scientists from the IBCh RAS Laboratory of Genomics of Adaptive Immunity has developed VDJviz – a multifunctional browser designed to work with large volumes of data produced using modern DNA sequence analysis. ...
Jul 28, 2016
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Investigators at Nationwide Children's Hospital have developed an analysis "pipeline" that slashes the time it takes to search a person's genome for disease-causing variations from weeks to hours. An article describing the ...
Jan 30, 2015
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Phen-Gen is the first computer analysis software that cross-references a patient's symptoms and a person's genome sequence, to better aid doctors in diagnosing diseases.
Aug 19, 2014
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A team of researchers led by Baylor College of Medicine have identified the gene underlying a newly recognized genetic syndrome that has symptoms of sleep apnea, delayed speech and hyptonia, or generalized upper body weakness.
May 1, 2014
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Scientists have used DNA sequencing for the first time to effectively track the spread of, and ultimately contain, an outbreak of methicillin-resistant Staphylococcus aureus (MRSA), according to new research published in ...
Nov 13, 2012
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Results of a study by Baylor College of Medicine physicians underscore the important role that clinical genetic evaluation can have in the management plan of patients with retinoblastoma, a childhood cancer of the eye.
Nov 14, 2011
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Researchers at the Swedish medical university Karolinska Institutet have discovered a new inherited disorder that causes severe mental retardation and liver dysfunction. The disease, adenosine kinase deficiency, is caused ...
Sep 30, 2011
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