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By performing whole genome sequencing, STAT-seq can help physicians make a more rapid diagnosis in patients who are acutely ill with a likely genetic disease. Another key aspect of the protocol is the ...

The first sequencing of the whole human genome in 2003 cost roughly $2.7 billion, but DNA sequencing giant Illumina has now unveiled a new machine that the company says is “expected one day ...

Starting today, Cambridge-based Veritas Genetics will be lowering its $999 whole genome sequencing and interpretation service for just $199 for two days, or to the first 1,000 people who buy spit ...

Illumina Genome Network will link researchers with its certified service providers. Illumina has established a new network initiative designed to link scientists looking to undertake large-scale ...

Illumina is launching a new software suite aimed at making it easier to identify the genetic factors behind various rare diseases. Using data gathered through whole-genome sequencing, the company ...

NEW YORK – Illumina and Harvard Pilgrim Health Care announced on Tuesday a risk-sharing agreement that will make whole-genome sequencing (WGS) available to certain Harvard Pilgrim patients ...

“If I get 10 samples of one mutation from 10 different patients, they’re all going to have different genetic backgrounds; they may behave differently. We’re trying to use the sequencing power that ...

Illumina, Inc. and Genpathway have announced the formation of a partnership to provide researchers whole-genome chromatin immunoprecipitation (ChIP) sequencing services. Samples are first prepared ...

Illumina will join with Nashville Biosciences and Amgen’s deCODE Genetics subsidiary to whole-genome sequence the largest-ever dataset of genomes from African-Americans—approximately 35,000 ...