Downloaded Stampy & BWA from http://www.well.ox.ac.uk/software-download-registration.
From the website:
Description: Stampy is a package for the mapping of short reads from illumina sequencing machines onto a reference genome. It's recommended for most workflows, including those for genomic resequencing, RNA-Seq and Chip-seq. Stampy excels in the mapping of reads containing that contain sequence variation relative to the reference, in particular for those containing insertions or deletions. It can map reads from a highly divergent species to a reference genome for instance. Stampy achieves high sensitivity and speed by using a fast hashing algorithm and a detailed statistical model. Stampy has the following features:
The reference paper for the package can be found here. I plan to use Stampy & BWA to map all my downloaded sequences to a reference strain of P. larvae DSM 25430, which I have also downloaded the fasta file from NCBI for. //EWW |
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