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Closing gaps in the human genome using sequencing by synthesis (2009)

Abstract
Abstract The most recent release of the finished human genome contains 260 euchromatic gaps (excluding chromosome Y). Recent work has helped explain a large number of these unresolved regions as 'structural' in nature. Another class of gaps is likely to be refractory to clone-based approaches, and cannot be approached in ways previously described. We present an approach for closing these gaps using 454 sequencing. As a proof of principle, we closed all three remaining non-structural gaps in chromosome 15.

Publication details
Download http://genomebiology.com/2009/10/6/R60
Publisher BioMed Central Ltd.
Repository BioMed Central (United Kingdom)
Type Method
Language English