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Next-Gen Sequencing tools from the Horvath Lab

ReadCounts tabulates the number of reads providing evidence for variant and reference nucleotides at specific genomic loci and applies statistical tests to recognize allelic read-counts consistent with homozygous and heterozygous loci.

ReadCounts is available as a self-contained binary package for 64-bit Linux and MacOS/Darwin systems and as Python source. The pysam package, plus a variety of common third-party python packages including numpy and scipy must be installed to use ReadCounts in Python source form. See the install instructions for more details. The self-contained binary package is appropriate for most Linux and MacOS users.

Setup:

Usage:

File Formats: