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パッケージ: mindthegap (2.2.3-4)

performs detection and assembly of DNA insertion variants in NGS read datasets

Designed to call insertions of any size, whether they are novel or duplicated, homozygous or heterozygous in the donor genome. It takes as input a set of reads and a reference genome. It outputs two sets of FASTA sequences: one is the set of breakpoints of detection insertion sites, the other is the set of assembled insertions for each breakpoint. MindTheGap can also be used as a genome assembly finishing tool. It can fill the gaps between a set of input contigs without any a priori on their relative order and orientation. It outputs the results in gfa file.

その他の mindthegap 関連パッケージ

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  • 提案
  • dep: libc6 (>= 2.34)
    GNU C Library: Shared libraries
    以下のパッケージによって提供される仮想パッケージでもあります: libc6-udeb
  • dep: libgatbcore3 (>= 1.4.2+dfsg-7)
    dynamic library of the Genome Analysis Toolbox
  • dep: libgcc-s1 (>= 3.3.1)
    GCC support library
  • dep: libhdf5-103-1
    HDF5 C runtime files - serial version
  • dep: libstdc++6 (>= 11)
    GNU Standard C++ Library v3

mindthegap のダウンロード

すべての利用可能アーキテクチャ向けのダウンロード
アーキテクチャ パッケージサイズ インストールサイズ ファイル
arm64 198.0 kB656 kB [ファイル一覧]