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Single Perfect Count for mapping reads to a lot of genomes

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spcount

This package is used to map short reads to multiple genomes with perfect match and report only once for each category.

Prerequisites

Install bowtie

BOWTIE_VERSION="1.2.3"
cd ~; \
  wget https://github.com/BenLangmead/bowtie/releases/download/v${BOWTIE_VERSION}/bowtie-${BOWTIE_VERSION}-linux-x86_64.zip; \
  unzip bowtie-${BOWTIE_VERSION}-linux-x86_64.zip; \
  rm bowtie-${BOWTIE_VERSION}-linux-x86_64.zip
export PATH=$PATH:~/bowtie-${BOWTIE_VERSION}-linux-x86_64

Installation

Install python main package

pip install spcount

Or you can install from github directly

pip install git+git://github.com/shengqh/spcount.git

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Single Perfect Count for mapping reads to a lot of genomes

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