Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Abstract

In both the HTML and PDF versions of this Data Descriptor, the author name Jason Flannick was incorrectly listed as Flannick Jason.

Tool evaluation for the detection of variably sized indels from next generation whole genome and targeted sequencing data

“…Compared with traditional Sanger capillary electrophoresis sequencing or other directed polymerase chain reaction-based screening methods, it provides a more efficient and affordable way to detect genomic variants in large scale [1][2][3]. NGS is widely used in research and in the clinic [4][5][6][7] and consists of techniques to cover the whole genome, i.e., whole genome sequencing (WGS), exome regions only, i.e., whole exome sequencing (WES), or certain genomic regions, i.e., targeted gene panel sequencing.…”

Variant calling tool evaluation for variable size indel calling from next generation whole genome and targeted sequencing data

“…Compared with traditional Sanger capillary electrophoresis sequencing, or other directed polymerase chain reactionbased screening methods, it provides a more efficient and affordable way to detect genomic variants in large scale [1][2][3]. NGS is widely used in research and in the clinic [4][5][6] and consists of techniques to cover the whole genome, i.e. whole genome sequencing (WGS), or only exome regions, i.e.…”