David Kaufman of the Genetics and Public Policy Center in Washington DC quizzed 1048 people who had paid for
genome scans by Decode Genetics of Reykjavik, Iceland, 23andMe of Mountain View, California, or Navigenics in Foster City, California.
Not exact matches
His team, as well as independent groups based in the UK, the US and Iceland, uncovered this gene's role
by comparing
genome - wide
scans of thousands of women with their age at menarche.
Bioinformaticians identified this protein and its potential connection to CRISPR
by scanning the public database of
genome sequences.
The $ 1,000
genome — brought to you
by CliffsNotes Heads up, Christmas shoppers: Icelandic company deCODE Genetics has launched a new service that, for a mere $ 985, will take your FedExed cheek swab and
scan the enclosed DNA for a sprinkling of genetic variations linked with 20 or so diseases, as well as ancestry and physical traits such as eye color (in case you don't have a mirror handy).
The bulk of them — 400,000 people whose
genomes had been
scanned for genetic markers — came from 23andMe, the company that offers genetic testing
by mail.
Researchers led
by Kari Stefansson at deCODE genetics in Reykjavik
scanned whole -
genome data from 1795 Icelanders for variations in APP that protect against Alzheimer's.
Genome - wide scans for selection have identified multiple regions of the human genome as being targeted by positive sele
Genome - wide
scans for selection have identified multiple regions of the human
genome as being targeted by positive sele
genome as being targeted
by positive selection.
By scanning the entire human
genome in search of genetic variations that may signal recent evolution, University of Chicago researchers found more than 700 genetic variants that may be targets of recent natural positive selection during the past 10,000 years of human evolution.
The short read aligner Bowtie has gone legitimate, with a publication last month in
Genome Biology and a mention
by GT's Daily
Scan.
Furthermore,
by chromatin immunoprecipitation and whole -
genome scanning approaches, we show that the chromosome ends of senescent cells directly contribute to the DNA damage response, and that uncapped telomeres directly associate with many, but not all, DNA damage response proteins.