diff options
author | scalavision <scalavision@gmail.com> | 2019-10-11 04:08:45 +0200 |
---|---|---|
committer | Dmitry Kalinkin <dmitry.kalinkin@gmail.com> | 2019-10-10 22:08:45 -0400 |
commit | 3d860972eefe10e04b7994d85f88dc7aeb6db248 (patch) | |
tree | b50210149cedde73f2bc64b3cbe3768711bfa28f /pkgs/applications/science | |
parent | 9cf81e9174ef3e4a1799a0dae9deffbdfc39a3fa (diff) | |
download | nixlib-3d860972eefe10e04b7994d85f88dc7aeb6db248.tar nixlib-3d860972eefe10e04b7994d85f88dc7aeb6db248.tar.gz nixlib-3d860972eefe10e04b7994d85f88dc7aeb6db248.tar.bz2 nixlib-3d860972eefe10e04b7994d85f88dc7aeb6db248.tar.lz nixlib-3d860972eefe10e04b7994d85f88dc7aeb6db248.tar.xz nixlib-3d860972eefe10e04b7994d85f88dc7aeb6db248.tar.zst nixlib-3d860972eefe10e04b7994d85f88dc7aeb6db248.zip |
delly: init at 0.8.1 (#70871)
Diffstat (limited to 'pkgs/applications/science')
-rw-r--r-- | pkgs/applications/science/biology/delly/default.nix | 40 |
1 files changed, 40 insertions, 0 deletions
diff --git a/pkgs/applications/science/biology/delly/default.nix b/pkgs/applications/science/biology/delly/default.nix new file mode 100644 index 000000000000..bfdf5a1bb17e --- /dev/null +++ b/pkgs/applications/science/biology/delly/default.nix @@ -0,0 +1,40 @@ +{ stdenv, fetchFromGitHub, htslib, zlib, bzip2, lzma, ncurses, boost }: + +stdenv.mkDerivation rec { + pname = "delly"; + version = "0.8.1"; + + src = fetchFromGitHub { + owner = "dellytools"; + repo = pname; + rev = "v${version}"; + sha256 = "18gm86j1g1k4z1cjv2m5v9rsl1xqs2w3dhwcsnzx2mhkrvmlc4i1"; + }; + + buildInputs = [ zlib htslib bzip2 lzma ncurses boost ]; + + EBROOTHTSLIB = htslib; + + installPhase = '' + runHook preInstall + + install -Dm555 src/delly $out/bin/delly + + runHook postInstall + ''; + + meta = with stdenv.lib; { + description = "Structural variant caller for mapped DNA sequenced data"; + license = licenses.gpl3; + maintainers = with maintainers; [ scalavision ]; + platforms = platforms.linux; + longDescription = '' + Delly is an integrated structural variant (SV) prediction method + that can discover, genotype and visualize deletions, tandem duplications, + inversions and translocations at single-nucleotide resolution in + short-read massively parallel sequencing data. It uses paired-ends, + split-reads and read-depth to sensitively and accurately delineate + genomic rearrangements throughout the genome. + ''; + }; +} |