GitHub - bayolau/discovardenovo: unofficial GIT tracking of the public release of DISCOVAR-denovo by Broad Institute's CRD team

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unofficial GIT tracking of the public release of DISCOVAR-denovo by Broad Institute's CRD team

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docs		docs
m4		m4
src		src
INSTALL		INSTALL
LICENSE		LICENSE
Makefile.am		Makefile.am
Makefile.in		Makefile.in
README		README
aclocal.m4		aclocal.m4
config.guess		config.guess
config.sub		config.sub
configure		configure
configure.ac		configure.ac
depcomp		depcomp
install-sh		install-sh
ltmain.sh		ltmain.sh
missing		missing

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DISCOVAR de novo
================

DISCOVAR de novo is a short read genome assembly developed by the Broad Institute. It can generate high quality assemblies from the latest 250 base Illumina paired-end PCR-free fragment reads.

DISCOVAR is undergoing continuous development. There is no 'official' release, instead please download the latest source code from our nightly builds. Check back often for updates.


The LICENSE file contains copyright and licensing information.

The INSTALL file contains information on how to configure, build, and install DISCOVAR de novo.


The docs directory contains documentation on DISCOVAR de novo and its associated tools:

    DiscovarDeNovo - DISCOVAR de novo manaul
    NhoodInfo      - NhoodInfo manual
    CrossOut       - CrossOut manual


For more information, visit the DISCOVAR blog:
http://www.broadinstitute.org/software/discovar/blog/

The above link includes directions on using the tool, along with other documentation.


-Computational R&D, The Broad Institute, Cambridge, MA
http://www.broadinstitute.org/science/programs/genome-biology/computational-rd/computational-research-and-development