Source: vg Maintainer: Debian Med Packaging Team Uploaders: Michael R. Crusoe Section: science Priority: optional Build-Depends: debhelper-compat (= 13), pv , bsdmainutils, zlib1g-dev, rs, libffi-dev, bwa , protobuf-compiler, libprotoc-dev, libprotobuf-dev, libjansson-dev, libbz2-dev, libncurses5-dev, automake, libtool, jq, samtools , unzip, librdf0-dev, cmake, pkg-config, bc, gtk-doc-tools, raptor2-utils , rasqal-utils , bison, flex, gawk, liblz4-dev, liblzma-dev, libcairo2-dev, libpixman-1-dev, libssw-dev, libdeflate-dev, libboost-program-options-dev, libjemalloc-dev, libbackward-cpp-dev, elfutils, libdw-dev, libelf-dev, libraptor2-dev, libsparsehash-dev, rapidjson-dev, libfml-dev, libfastahack-dev, fastahack , tabix , xxd , libsmithwaterman-dev, libdivsufsort-dev, libtsl-hopscotch-map-dev, libvcflib-dev (>= 1.0.1), libvcflib-tools , libhts-dev, help2man , python3:any, libsimde-dev # libsdsl-dev, # libvw-dev, # redland-utils, # not needed? Build-Depends-Indep: doxygen , graphviz Standards-Version: 4.5.1 Vcs-Browser: https://salsa.debian.org/med-team/vg Vcs-Git: https://salsa.debian.org/med-team/vg.git Homepage: https://github.com/vgteam/vg#vg Rules-Requires-Root: no Package: vg Built-Using: ${simde:Built-Using} Architecture: amd64 arm64 ppc64el mips64el s390x riscv64 x32 Depends: ${shlibs:Depends}, ${misc:Depends} Conflicts: cgvg Description: tools for working with genome variation graphs variation graph data structures, interchange formats, alignment, genotyping, and variant calling methods . Variation graphs provide a succinct encoding of the sequences of many genomes. A variation graph (in particular as implemented in vg) is composed of: . - nodes, which are labeled by sequences and ids - edges, which connect two nodes via either of their respective ends - paths, describe genomes, sequence alignments, and annotations (such as gene models and transcripts) as walks through nodes connected by edges . This model is similar to a number of sequence graphs that have been used in assembly and multiple sequence alignment. Paths provide coordinate systems relative to genomes encoded in the graph, allowing stable mappings to be produced even if the structure of the graph is changed. Package: vg-docs Architecture: all Section: doc Multi-Arch: foreign Depends: ${misc:Depends} Description: tools for working with genome variation graphs -- docs variation graph data structures, interchange formats, alignment, genotyping, and variant calling methods . Variation graphs provide a succinct encoding of the sequences of many genomes. A variation graph (in particular as implemented in vg) is composed of: . - nodes, which are labeled by sequences and ids - edges, which connect two nodes via either of their respective ends - paths, describe genomes, sequence alignments, and annotations (such as gene models and transcripts) as walks through nodes connected by edges . This model is similar to a number of sequence graphs that have been used in assembly and multiple sequence alignment. Paths provide coordinate systems relative to genomes encoded in the graph, allowing stable mappings to be produced even if the structure of the graph is changed. . This package provides the documentation