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Targeted and Mapping-Free Variant Calling in FastQ Reads of Bacterial Genomes

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KvarQ: Targeted and direct variant calling in FastQ reads of bacterial genomes

The program KvarQ performs rapid in silico genotyping for selected loci (e.g. phylogenetic SNPs, drug resistance mutations) in bacterial genome sequences in FastQ format. Mapping to a whole-genome reference sequence or de novo assembly or the short reads is not necessary.

Some example testsuites can be found in the testsuites/ subdirectory.

KvarQ is written in Python and C, is open-source and published under GNU GPLv3.

Pre-compiled packages are available for Windows 7 or later, and for Mac OS X (10.6 or later) can be downloaded from the Swiss TPH website.

Documentation

For more information refer to the online documentation.

KvarQ: targeted and direct variant calling from fastq reads of bacterial genomes. Steiner A, Stucki D, Coscolla M, Borrell S, Gagneux S. BMC Genomics. 2014 Oct 9;15(1):881. doi: 10.1186/1471-2164-15-881. http://www.swisstph.ch/kvarq.

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Targeted and Mapping-Free Variant Calling in FastQ Reads of Bacterial Genomes

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