VikNGS: a C++ variant integration kit for next generation sequencing association analysis.
other · Level V
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- Record sourced from PubMed, PMID 31580400.
- Also identified by DOI 10.1093/bioinformatics/btz716 and PMC identifier 7703770.
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Abstract
Integration of next generation sequencing data (NGS) across different research studies can improve the power of genetic association testing by increasing sample size and can obviate the need for sequencing controls. If differential genotype uncertainty across studies is not accounted for, combining datasets can produce spurious association results. We developed the Variant Integration Kit for NGS (VikNGS), a fast cross-platform software package, to enable aggregation of several datasets for rare and common variant genetic association analysis of quantitative and binary traits with covariate adjustment. VikNGS also includes a graphical user interface, power simulation functionality and data visualization tools. The VikNGS package can be downloaded at http://www.tcag.ca/tools/index.html. Supplementary data are available at Bioinformatics online.
Medical subject headings
- High-Throughput Nucleotide Sequencing
- Software