A framework for the estimation of the proportion of true discoveries in single nucleotide variant detection studies for human data - supplemental files

<br>The data were originally downloaded from Bioplanet’s Genome Comparison &amp; Analytic Testing (GCAT) tool website that is no longer functioning:<br>https://www.biostars.org/p/69341/The files contain Illumina reads from a targeted exome sequencing of the well known NA12878 sample with TrueSeq sequencing kit. The original files names are preserved.There are five files in total:<br>gcat_set_025_*.fastq - two files with 30X coveragegcat_set_053_*.fastq - two files with 150X coveragegcat_set_025.bed - target region from TrueSeq kit (about 45 Megabases). Bioplanet also provided a file named gcat_set_053.bed for 150X coverage, but these two files are identical.<strong><br></strong><strong><br></strong><strong><br></strong><br><br>