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[ Source: pirs  ]

Paketti: pirs (2.0.2+dfsg-9)

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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.

Muut pakettiin pirs liittyvät paketit

  • depends
  • recommends
  • suggests
  • enhances

Imuroi pirs

Imurointi kaikille saataville arkkitehtuureille
Arkkitehtuuri Paketin koko Koko asennettuna Tiedostot
amd64 113.3 kt392.0 kt [tiedostoluettelo]
arm64 105.1 kt364.0 kt [tiedostoluettelo]
armel 101.5 kt350.0 kt [tiedostoluettelo]
armhf 101.4 kt302.0 kt [tiedostoluettelo]
i386 121.7 kt402.0 kt [tiedostoluettelo]
mips64el 114.1 kt427.0 kt [tiedostoluettelo]
mipsel 116.6 kt412.0 kt [tiedostoluettelo]
ppc64el 115.1 kt420.0 kt [tiedostoluettelo]
s390x 106.1 kt384.0 kt [tiedostoluettelo]