套件： ncbi-epcr (2.3.12-1-9)
ncbi-epcr 的相關超連結
Trisquel 的資源：
下載原始碼套件 epcr：
維護者：
Original Maintainers:
- Debian Med Packaging Team (郵件存檔)
- Steffen Moeller
- Andreas Tille
- Charles Plessy
外部的資源：
- 主頁 [www.ncbi.nlm.nih.gov]
相似套件：
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.
其他與 ncbi-epcr 有關的套件
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- dep: libc6 (>= 2.14) [amd64]
- GNU C Library: Shared libraries
同時作為一個虛擬套件由這些套件提供： libc6-udeb
- dep: libc6 (>= 2.17) [arm64, ppc64el]
- dep: libc6 (>= 2.4) [armhf]
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- dep: libgcc-s1 (>= 3.0) [amd64]
- GCC support library
- dep: libgcc-s1 (>= 3.5) [armhf]
- dep: libgcc-s1 (>= 4.2) [arm64, ppc64el]
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- dep: libstdc++6 (>= 5.2)
- GNU Standard C++ Library v3
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- sug: bioperl
- Perl tools for computational molecular biology