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[ Source: epcr  ]

Package: ncbi-epcr (2.3.12-1-9)

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Tool to test a DNA sequence for the presence of sequence tagged sites

Electronic PCR (e-PCR) is computational procedure that is used to identify sequence tagged sites(STSs), within DNA sequences. e-PCR looks for potential STSs in DNA sequences by searching for subsequences that closely match the PCR primers and have the correct order, orientation, and spacing that could represent the PCR primers used to generate known STSs.

The new version of e-PCR implements a fuzzy matching strategy. To reduce likelihood that a true STS will be missed due to mismatches, multiple discontiguous words may be used instead of a single exact word. Each of this word has groups of significant positions separated by 'wildcard' positions that are not required to match. In addition, it is also possible to allow gaps in the primer alignments.

The main motivation for implementing reverse searching (called Reverse e-PCR) was to make it feasible to search the human genome sequence and other large genomes. The new version of e-PCR provides a search mode using a query sequence against a sequence database.

This program is retired upstream and it is suggested to use Primer-Blast

 https://www.ncbi.nlm.nih.gov/tools/primer-blast/
instead.

Tags: Field: Biology, Bioinformatics, Implemented in: implemented-in::c++, interface::commandline, Role: Program, Scope: Utility, Purpose: use::checking, use::searching, Supports Format: Plain Text, Works with: Need an extra tag

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Download for all available architectures
Architecture Package Size Installed Size Files
amd64 164.4 kB496.0 kB [list of files]
arm64 153.9 kB460.0 kB [list of files]
armel 143.5 kB416.0 kB [list of files]
armhf 144.3 kB332.0 kB [list of files]
i386 172.0 kB512.0 kB [list of files]
mips64el 162.7 kB594.0 kB [list of files]
ppc64el 167.9 kB692.0 kB [list of files]
s390x 153.5 kB496.0 kB [list of files]