New Publication: NCL prevalence 2016 – 22 August 2016
Our study on determining the prevalence of neuronal ceroid lipofuscinosis using ExAC whole exome sequencing data is published in Gene.
New Publication: Biploar I Disorder 2016 – 02 August 2016
Our study on Bipoloar I Disorder in a multiplex family using Whole Genome Sequencing is published in Molecular Neuropsychiatry.
New Publication: ME-Scan-SVA 2016 – 01 August 2016
Our study on SVA elements using the Mobile Element Scanning (ME-Scan) method is published in Mobile DNA.
New Publication: Worldwide Wolf Diversity 2016 – 02 February 2016
Our study on the world wide grey wolf diversity and admixture is published in Genome Research.
New Grant: NIH Genome Sequencing Program – 26 January 2016
The NIH Genome Sequencing Program is officially announced (Press Release). Rutgers (PI Tara Matise and Steven Buyske, Co-I Jinchuan Xing) received a $3.8 million grant from NHGRI to run the coordinating center of the program.
New Publication: COPD WES 2016 – 07 January 2016
Our study on whole-exome sequencing based COPD disease gene identification is published in Human Genomics.