Columbia University's Laboratory of Personalized Genomic Medicine has launched a whole-exome sequencing test for inherited genetic disorders, likely the first such test with conditional approval from the New York State Department of Health.

In addition to offering the exome test and an existing mitochondrial genome sequencing test, the lab is working on other NGS-based diagnostics – among them a 1,000-gene "superpanel," a whole-genome sequencing test, and a cancer panel – all of which it plans to release later this year.

Get the full story with
GenomeWeb Premium

Only $95 for the
first 90 days*

A trial upgrade to GenomeWeb Premium gives you full site access, interest-based email alerts, access to archives, and more. Never miss another important industry story.

Try GenomeWeb Premium now.

Already a GenomeWeb Premium member? Login Now.
Or, See if your institution qualifies for premium access.

*Before your trial expires, we’ll put together a custom quote with your long-term premium options.

Not ready for premium?

Browse our free articles
You can still register for access to our free content.

The Guardian discusses whether big science projects are worth the loss of resources available for other scientific pursuits.

An NEJM update from the ClinVar team highlights the difficulties of interpreting genetic variants.

In Nature this week: genomic analysis of high-grade serous ovarian cancer, and more.

The new Riken president outlines some of his plans for the institute.