Objective

To promote the utilization of cutting-edge next-generation sequencing technology for the identification of genes involved in rare disorders with a clear genetic basis and to provide support for the Spanish research community.

The results will be published as a collaborative effort between the applicant's group and the supporting investigators.

Eligibility

Researchers working at Spain universities, public research institutes and hospitals

Applicants must hold a PhD or MD degree and a work contract with the host institution at the time of application

Applicants must have their own research lines and experience in leading research groups

Applicants must not hold awards directly related to Whole Exome Sequencing in the proposed group of disorders.

How to apply

See attached document.

In case of interest, contact with Research's Unit before 8th January.

The proposal will be sent to: info_cnag@pcb.ub.cat with "2013 CNAG CALL: 300 EXOMES TO ELUCIDATE RARE DISEASES" in subject line.