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Fig. 4 | BMC Bioinformatics

Fig. 4

From: Rare copy number variant analysis in case–control studies using snp array data: a scalable and automated data analysis pipeline

Fig. 4

Pipeline performance. Calling and QC analysis sub-pipeline and rare-CNVs analysis sub-pipeline for 6,112 samples, 700,079 markers (genotyping data from Illumina GSA), and 98,702 calls detected. Time in seconds, in logarithmic scale, is plotted for each module-rule. Calling and QC analysis runtime was 72.31 h (260,320 s), and rare CNVs analysis runtime was 21.5 min (1290 s)

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BMC Bioinformatics

ISSN: 1471-2105

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