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[ 原始碼: soapsnp  ]

套件:soapsnp(1.03-5)

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resequencing utility that can assemble consensus sequence of genomes

For getting ideas on the cause of diseases or their response to therapy, and for understanding either for a particular patient, doctors around the globe are starting to look at the genes or the whole genome and how that sequence is different from a healthy / well responding individual.

SOAPsnp is a member of the SOAP (Short Oligonucleotide Analysis Package). The program is a resequencing utility. It assembles the consensus sequence for the genome of a newly sequenced individual based on the alignment of the raw sequencing reads on a known reference. SNPs can then be identified on the consensus sequence through the comparison with the reference.

SOAPsnp uses a method based on Bayes' theorem (the reverse probability model) to call consensus genotype by carefully considering the data quality, alignment, and recurring experimental errors. All these kinds of information was integrated into a single quality score for each base in PHRED scale to measure the accuracy of consensus calling. Currently, it supports the alignment format of SOAPaligner (soap2).

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硬體架構 套件大小 安裝後大小 檔案
amd64 48。6 kB118。0 kB [檔案列表]
arm64 43。5 kB146。0 kB [檔案列表]
armel 41。2 kB97。0 kB [檔案列表]
armhf 40。3 kB77。0 kB [檔案列表]
i386 48。6 kB117。0 kB [檔案列表]
mips64el 49。3 kB149。0 kB [檔案列表]
mipsel 49。6 kB147。0 kB [檔案列表]
ppc64el 52。4 kB146。0 kB [檔案列表]
s390x 46。8 kB122。0 kB [檔案列表]