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(P3) Next Generation Human Genetics

Journal article published in 2013 by Jay Shendure ORCID
This paper is available in a repository.
This paper is available in a repository.

Full text: Download

Question mark in circle
Preprint: policy unknown
Question mark in circle
Postprint: policy unknown
Question mark in circle
Published version: policy unknown

Abstract

Our lab is broadly interested in the development of new technologies in genomics and molecular biology. In my talk, I will describe new technologies with particular relevance for disease gene discovery and the clinical application of genomics, including exome and targeted sequencing for studying Mendelian and complex disease, massively parallel functional assays, haplotype-resolved genome sequencing, and non-invasive whole genome fetal sequencing.