NEW YORK (GenomeWeb News) – Researchers and clinicians around the globe who are looking for a genetic basis for any number of rare diseases have a new resource to turn to — a web portal for genetic and phenotypic information on rare diseases developed through an international collaboration and funded by several Canadian entities.

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In Genome Research this week: multiplex genotyping of germline and somatic short tandem repeats, graph-based regularization, and more.

A lack of funding may lead more than two dozen research facilities in Australia to shut down in three months.

Researchers report that paternally inherited genes are more likely to be expressed in mice.

The US Supreme Court has declined to review a decision involving the use of "inadvertently shed" DNA in a police investigation and subsequent conviction.