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[ Fonte: pirs  ]

Pacote: pirs (2.0.2+dfsg-11)

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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 de pirs

Baixe para todas as arquiteturas disponíveis
Arquitetura Tamanho do pacote Tamanho instalado Arquivos
amd64 114.9 kB395.0 kB [lista de arquivos]
arm64 106.4 kB423.0 kB [lista de arquivos]
armel 102.8 kB421.0 kB [lista de arquivos]
armhf 102.6 kB357.0 kB [lista de arquivos]
i386 123.2 kB405.0 kB [lista de arquivos]
mips64el 115.6 kB498.0 kB [lista de arquivos]
mipsel 117.6 kB431.0 kB [lista de arquivos]
ppc64el 117.2 kB423.0 kB [lista de arquivos]
s390x 107.4 kB387.0 kB [lista de arquivos]