Genomic Analysis Platform Offers Insights into Health, Disease

It can also generate up to 240 million sequence tags per run, which is expected to reduce the cost of conducting sequencing-based gene expression applications further.

Scientists at the Broad Institute of the Massachusetts Institute of Technology (MIT) and Harvard (Cambridge, MA, USA) are using two SOLiD systems for large-scale discovery of genetic variation in human genome samples, as part of the Broad Institute's contribution to the 1000 Genomes Project, a worldwide effort to create the most detailed and medically useful picture of human genetic variation to date. The scientists generated more than 50 billion bases of DNA sequence over just six weeks.

At Columbia University Medical Center (CUMC; New York, NY, USA), scientists have been using the SOLiD system for a novel approach to study whole-genome methylation profiles in a panel of breast cancer tumors, benefiting from the mate-pair analysis capabilities of the system to map the methylation state of all regions of the genome.

The institutes presented their preliminary findings at the Cold Spring Harbor Laboratory's Biology of Genomes meeting in New York (USA) from May 6-10, 2008.


Related Links:
Columbia University Medical Center
Applied Biosystems
Broad Institute of MIT and Harvard