Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing.

ABSTRACT:

Background

To facilitate the clinical implementation of genomic medicine by next-generation sequencing, it will be critically important to obtain accurate and consistent variant calls on personal genomes. Multiple software tools for variant calling are available, but it is unclear how comparable these tools are or what their relative merits in real-world scenarios might be.

Methods

We sequenced 15 exomes from four families using commercial kits (Illumina HiSeq 2000 platform and Agilent SureSelect version 2 capture kit), with approximately 120X mean coverage. We analyzed the raw data using near-default parameters with five different alignment and variant-calling pipelines (SOAP, BWA-GATK, BWA-SNVer, GNUMAP, and BWA-SAMtools). We additionally sequenced a single whole genome us

SUBMITTER: O'Rawe J 

PROVIDER: S-EPMC3706896 | biostudies-literature | 2013

REPOSITORIES: biostudies-literature