Impact on variant calling of increased sequencing depth. Anne Bruun Krøigård Mads Thomassen Anne-Vibeke Lænkholm Torben A. Kruse Martin Jakob Larsen 10.1371/journal.pone.0151664.g004 https://plos.figshare.com/articles/figure/Impact_on_variant_calling_of_increased_sequencing_depth_/3136654 <p>The impact on variant calling of increased sequencing depth for SNV and indel calling are shown in left and right panels, respectively. The number of called positions called in exome sequencing only, validation data only and both data set, depicted in blue, green and red, respectively. This analysis only includes regions that are successfully covered (at least 200 x) in the deep sequencing data.</p> 2016-03-22 06:26:58 Somatic variant callers breast cancer patients exome sequencing SNV variant callers Targeted Deep Sequencing Data mutation sequencing data Somatic Variant Callers