Resource Library

CDS Tools

A Template for Authoring and Adapting Genomic Medicine Content in the eMERGE Infobutton Project – Toward establishing such an information model among information resources developed by eMERGE institutions, we have prepared this template that contains important content topics for genomic medicine.

ANNOVAR – Annotates genetic variants detected from genomes that can shortlist SNVs and insertions/deletions, examine and report functional consequence, infer cytogenetic bonds, find variants in conserved regions, and identify variants from the 1000 Genomes Project and dbSNP. Widely used: 394 citations to date.

MyResearch, integration between Registrar and MyChart

In the News

Here's what's happening with eMerge:

08
OCT

NIH Office of Disease Prevention’s 2020 Early Stage Investigator Lecture

Call for Nominations!

Office...

08
OCT

Health Data Management (10/8) reports that National Library of Medicine (NLM) Director Patricia Flatley Brennan “told a House appropriations subcommittee late last month that NLM is working on tools...

29
AUG

Headed to ASHG in Houston this October? NHGRI is hosting a free ancillary workshop that will help clear up some of the mysteries of applying for grants at the NIH! The Early...

27
AUG

eMERGE Network is excited to share that the MCS NT244, Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network; was published on August 22nd to American Journal of Human...