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Researchers have successfully employed an algorithm to identify potential mutations which increase disease risk in the noncoding regions our DNA, which make up the vast majority of the human genome.
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News-Medical.Net on MSNResearchers use algorithm to pinpoint disease risk mutations in noncoding DNAResearchers from Children's Hospital of Philadelphia (CHOP) and the Perelman School of Medicine at the University of ...
Researchers from Children's Hospital of Philadelphia (CHOP) and the Perelman School of Medicine at the University of ...
A seminal study has uncovered a new genetic cause of neurodevelopmental disorders (NDDs). The discovery offers both closure and hope to potentially thousands of families worldwide who have long been ...
University of Delaware's Mona Batish is a molecular biologist. She studies circular RNAs formed as a result of so-called ...
Researchers have identified mutations in the non-coding gene RNU2-2 as a cause of a newly defined neurodevelopmental disorder ...
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