Tools

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:

06
DEC

eMERGE Network is excited to share that Taryn Hall's project, Unfolding of hidden white blood cell count phenotypes for gene discovery using latent class mixed modeling; was published in Genes...

20
JUL

eMERGE Network is excited to share that Dr. Douglas Pet's project, Physicians Raise Concerns on Receiving Unsolicited Genomic Results; was published in Genetics in Medicine. The publication...

14
MAY

CDC's new blog post: Precision Medicine in Action: How well does cascade screening for hereditary conditions work in the real world? Posted on May 8, 2018 by 

23
APR

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