Catherine A McCarty

No ORCID on file · 3 papers in corpus
other 2016
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing ·doi:10.1142/9789814749411_0024

Next-generation sequencing technology has presented an opportunity for rare variant discovery and association of these variants with disease. To address the challenges of rare variant analysis, multiple statistical methods have been develop…

observational 2012
International Journal of Gynecology & Obstetrics ·doi:10.1016/j.ijgo.2011.10.003

OBJECTIVE: To establish a well-defined cohort for genetic epidemiology studies of endometriosis and conduct a pilot study to confirm validity using existing data associated with endometriosis. METHODS: Between January and May 2010, a neste…

other 2009
BMC medical genomics ·doi:10.1186/1755-8794-2-17

BACKGROUND: For population based biorepositories to be of use, rigorous quality control and assurance must be maintained. We have designed and validated a panel of polymorphisms for individual sample identification consisting of 36 common p…