The presence of duplicates introduced by PCR amplification is a major issue in paired short reads from next-generation sequencing platforms. These duplicates might have a serious impact on research applications, such as scaffolding in whole-genome sequencing and discovering large-scale genome variations, and are usually removed. We present FastUniq as a fast
Publisher: Public Library of Science
Date Published: 20-December-2012
Author(s): Xu H., Luo X., Qian J., Pang X., Song J., Qian G., Chen J., Chen S.