By a GenomeWeb staff reporter

NEW YORK (GenomeWeb News) – A new study appearing online last night in the Proceedings of the National Academy of Sciences suggests target-enriched high-throughput sequencing can be used to help find variants behind some forms of hereditary hearing loss.

Get the full story

This story is free
for registered users

Registering provides access to this and other free content.

Register now.

Already have an account?
Login Now.

David Dobbs writes at Buzzfeed that genomics has delivered little on its promises.

In PNAS this week: co-evolutionary signatures of insect hosts and bacterial symbionts, distinct transcript isoforms of high-grade ovarian cancer, and more.

Adam Rutherford discusses genetic genealogy at the Guardian.

Portions of the US 21st Century Cures Act are raising some safety concerns.