American Society of Human Genetics
New method helps link genomic variation to protein production
Scientists have adopted a novel laboratory approach for determining the effect of genetic variation on the efficiency of the biological process that translates a gene's DNA sequence into a protein, such as hemoglobin, according ...
Genetics
Nov 06, 2012 |
4.3 / 5 (3) |
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Unexplained intellectual disability explained by state-of-the-art genetic analysis
A research team reported that next generation sequencing of the exome, the 1 to 2% of the DNA containing the genes that code for proteins, enabled the identification of the genetic causes of unexplained intellectual disability ...
Genetics
Nov 08, 2012 |
4 / 5 (3) |
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Significant relationship between mortality and telomere length discovered
A team of researchers at Kaiser Permanente and the University of California, San Francisco (UCSF) has identified a significant relationship between mortality and the length of telomeres, the stretches of DNA that protect ...
Genetics
Nov 08, 2012 |
4.5 / 5 (2) |
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Whole genome sequencing of de novo balanced rearrangements in prenatal diagnosis
Whole genome sequencing of the DNA code of three prenatal samples provided a detailed map of the locations of their chromosomal abnormalities in 14 days, scientists reported today at the American Society of Human Genetics ...
Genetics
Nov 07, 2012 |
5 / 5 (1) |
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Exome sequencing: Potential diagnostic assay for unexplained intellectual disability
Research findings confirming that de novo mutations represent a major cause of previously unexplained intellectual disability were presented on Nov. 8 at the American Society of Human Genetics 2012 meeting in San Francisco.
Genetics
Nov 08, 2012 |
5 / 5 (1) |
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DNA variants explain over 10 percent of inherited genetic risk for heart disease
About 10.6% of the inherited genetic risk for developing coronary artery disease (CAD) can be explained by specific DNA variations, according to research reported today at the American Society of Human Genetics 2012 meeting.
Genetics
Nov 08, 2012 |
5 / 5 (1) |
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Novel type 2 diabetes genetic study involves five major ancestry groups
A consortium of scientists who are taking a novel approach in their research to detect the genetic variations that predispose individuals to type 2 diabetes provided an update of their findings at the American Society of ...
Genetics
Nov 08, 2012 |
5 / 5 (1) |
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Surprising findings from Exome Sequencing Project reported
A multi-institutional team of researchers has sequenced the DNA of 6,700 exomes, the portion of the genome that contains protein-coding genes, as part of the National Heart, Lung and Blood Institute (NHLBI)-funded Exome Sequencing ...
Genetics
Nov 06, 2012 |
4 / 5 (1) |
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