Thousands of never-before-seen genetic variants in the human genome have been uncovered using a new genome sequencing technology. These discoveries close many human genome mapping gaps that have long resisted sequencing.
Nov 10, 2014
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(AP) -- George Eberhardt turned 107 last month, and scientists would love to know how he and other older folks like him made it that far. So he's going to hand over some of his DNA. He's one of 100 centenarians taking part ...
Oct 26, 2011
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What type of brain tumor does this patient have? AI technology helps to determine this as early as during surgery, within 1.5 hours. This process would normally take a week. The new technology allows neurosurgeons to adjust ...
Oct 11, 2023
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A new study, "Sensitive poliovirus detection using nested PCR and nanopore sequencing: a prospective validation study," published 17 August 2023 in Nature Microbiology, proves that using DDNS to detect polio outbreaks can ...
Aug 21, 2023
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The stretches of DNA that differ from person to person, called variants, are a major part of what makes us unique, but they can also put us at greater risk of disease. Although we can currently spell out between 80% and 90% ...
Feb 7, 2022
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Working alongside colleagues in Mainz, Bern, Hannover and Bonn, researchers from Charité - Universitätsmedizin Berlin, the Berlin Institute of Health (BIH) and the German Rheumatism Research Center Berlin (DRFZ) were able ...
May 12, 2020
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Researchers from the European Bioinformatics Institute (EMBL-EBI), University of Cambridge, the Wellcome Trust Sanger Institute and the Cancer Research UK-Cambridge Institute (CRUK-CI) have shed light on a long-standing debate ...
Mar 30, 2017
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People with achromatopsia, an inherited eye disorder, see the world literally in black and white. Worse yet, their extreme sensitivity to light makes them nearly blind in bright sunlight. Now, researchers at University of ...
Jun 1, 2015
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A new gene sequencing technology allows us to explore the human genome at a much higher resolution than ever before, with revolutionary implications for research and cancer diagnosis.
Mar 9, 2015
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(Medical Xpress)—A new diagnostic test may be around the corner thanks to the discovery of a gene mutation that marks the progression from a harmless oesophageal condition to cancer, according to research published in Nature ...
Jun 23, 2014
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