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......@@ -29,3 +29,22 @@ Description: Performs detection and assembly of DNA insertion variants in NGS re
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.
Package: mindthegap-examples
Architecture: all
Depends: ${shlibs:Depends},
${misc:Depends},
${python3:Depends}
mindthegap
Description: Optional scripts and example resources for mindthegap.
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 gap between a set of input contigs
without any a priori on their relative order and orientation. It
outputs the results in gfa file. Please note that this package is
meant to accommodate the mindthegap package and only acts as example
to how this package can be utilised.
scripts usr/share/doc/mindthegap
test/scripts usr/share/doc/mindthegap
test/vde.py usr/share/doc/mindthegap
......@@ -5,7 +5,6 @@ test/references usr/share/mindthegap/test
test/truths usr/share/mindthegap/test
test/*.sh usr/share/mindthegap/test
test/eval.cpp usr/share/mindthegap/test
test/vde.py usr/share/mindthegap/test
test/contig_test/*.fasta usr/share/mindthegap/test/contig_test
test/contig_test/*.info.txt usr/share/mindthegap/test/contig_test
test/contig_test/*gfa usr/share/mindthegap/test/contig_test
......@@ -15,8 +14,7 @@ test/full_test/*.breakpoints usr/share/mindthegap/test/full_test
test/full_test/*.output usr/share/mindthegap/test/full_test
test/full_test/*.*.vcf usr/share/mindthegap/test/full_test
data usr/share/mindthegap
scripts usr/share/doc/mindthegap
CHANGELOG.md usr/share/doc/mindthegap
README.md usr/share/doc/mindthegap
debian/tmp/usr/bin/MindTheGap usr/bin