News and updates

Far into the research process, CSER has much to share at the ACMG 2022 meeting over Mar 22-26 2022! Read more »

Come check out a number of high-impact CSER work at the ASHG 2021 Annual Meeting! Read more »

CSER is leading a number of posters and presentations at ACMG 2021. Come check us out! Read more »

CSER researchers are excited to share that a collaborative project between CSER and eMERGE exploring genomic variant classification concordance is out now! Read more »

CSER at the ASHG 2020 Virtual Meeting! Read more »

Posters galore at ASHG 2019! Read more »

Coming to ACMG 2019: CSER! Read more »

Come check out CSER efforts at ASHG 2018! Read more »

An extensive look into CSER1's experiences with secondary findings reveals how SFs impact unrecognized family history, causes little distress on patients, and induce modest 1-year downstream costs. Read more »

Out now, the CSER Marker Paper, describing the work of CSER in addressing evidence gaps in delivering genomics in non-academic settings and diverse populations. Read more »

Learn more about CSER Phase 1 and CSER Phase 2 at ACMG 2018! Read more »

Come check out CSER research at the American Society of Human Genetics 2017 Annual Meeting! Read more »

Six sites and one coordinating center are funded as part of CSER. Focusing on diverse populations, sites seek to generate evidence supporting use of genomic sequencing in medical care. Read more »