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[ Source: pirs  ]

Package: pirs (2.0.2+dfsg-12)

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Profile based Illumina pair-end Reads Simulator

The program pIRS can be used for simulating Illumina PE reads, with a series of characters generated by Illumina sequencing platform, such as insert size distribution, sequencing error(substitution, insertion, deletion), quality score and GC content-coverage bias.

The insert size follows a normal distribution, so users should set the mean value and standard deviation. Usually the standard deviation is set as 1/20 of the mean value. The normal distribution by Box-Muller method is simulated.

The program simulates sequencing error, quality score and GC content- coverage bias according to the empirical distribution profile. Some default profiles counted from lots of real sequencing data are provided.

To simulate reads from diploid genome, users should simulate the diploid genome sequence firstly by setting the ratio of heterozygosis SNP, heterozygosis InDel and structure variation.

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Download pirs

Download for all available architectures
Architecture Package Size Installed Size Files
amd64 116.7 kB390.0 kB [list of files]
arm64 106.7 kB422.0 kB [list of files]
armel 102.8 kB352.0 kB [list of files]
armhf 102.6 kB304.0 kB [list of files]
i386 122.5 kB392.0 kB [list of files]
mips64el 115.4 kB432.0 kB [list of files]
ppc64el 117.0 kB422.0 kB [list of files]
s390x 113.8 kB390.0 kB [list of files]