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[ 原始碼: pirs  ]

套件:pirs(2.0.2 dfsg-8)

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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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下載 pirs

下載可用於所有硬體架構的
硬體架構 套件大小 安裝後大小 檔案
amd64 109。7 kB375。0 kB [檔案列表]
arm64 101。6 kB351。0 kB [檔案列表]
armhf 98。4 kB293。0 kB [檔案列表]
i386 117。0 kB381。0 kB [檔案列表]