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Commits on Source (2)
add man page building
· 1b0b8408
Sascha Steinbiss
authored
Jan 09, 2020
1b0b8408
install manpages
· f30ceda8
Sascha Steinbiss
authored
Jan 09, 2020
f30ceda8
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debian/copyright
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f30ceda8
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@@ -39,7 +39,7 @@ Copyright: (c) 2003-2009 Gordon Gremme <gordon@gremme.org>
(c) 2003-2008 Center for Bioinformatics, University of Hamburg
License: ISC
File: src/gth/editoperation.h
File
s
: src/gth/editoperation.h
Copyright: (c) 2003-2009 Gordon Gremme <gordon@gremme.org>
(c) 2003 Stefan Kurtz <kurtz@zbh.uni-hamburg.de>
(c) 2003-2007 Center for Bioinformatics, University of Hamburg
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debian/genomethreader.manpages
0 → 100644
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f30ceda8
debian/man/*.1
debian/man_src/gth.1.adoc
0 → 100644
View file @
f30ceda8
# gth(1)
## NAME
gth - calculate genome structures
## SYNOPSIS
*gth* [option ...] -genomic file [...] -cdna file [...] -protein file [...]
## DESCRIPTION
Computes similarity-based gene structure predictions (spliced alignments)
using cDNA/EST and/or protein sequences and assemble the resulting spliced
alignments to consensus spliced alignments.
## OPTIONS
-genomic specify input files containing genomic sequences
mandatory option
-cdna specify input files containing cDNA/EST sequences
-protein specify input files containing protein sequences
-species specify species to select splice site model which is most
appropriate; possible species:
"human"
"mouse"
"rat"
"chicken"
"drosophila"
"nematode"
"fission_yeast"
"aspergillus"
"arabidopsis"
"maize"
"rice"
"medicago"
default: undefined
-bssm read bssm parameter from file in the path given by the
environment variable BSSMDIR
default: undefined
-scorematrix read amino acid substitution scoring matrix from file in the
path given by the environment variable GTHDATADIR
default: BLOSUM62
-translationtable set the codon translation table used for codon translation in
matching, DP, and output
default: 1
-f analyze only forward strand of genomic sequences
default: no
-r analyze only reverse strand of genomic sequences
default: no
-cdnaforward align only forward strand of cDNAs
default: no
-frompos analyze genomic sequence from this position
requires -topos or -width; counting from 1 on
default: 0
-topos analyze genomic sequence to this position
requires -frompos; counting from 1 on
default: 0
-width analyze only this width of genomic sequence
requires -frompos
default: 0
-v be verbose
default: no
-xmlout show output in XML format
default: no
-gff3out show output in GFF3 format
default: no
-md5ids show MD5 fingerprints as sequence IDs
default: no
-o redirect output to specified file
default: undefined
-gzip write gzip compressed output file
default: no
-bzip2 write bzip2 compressed output file
default: no
-force force writing to output file
default: no
-gs2out output in old GeneSeqer2 format
default: no
-minmatchlen specify minimum match length (cDNA matching)
default: 20
-seedlength specify the seed length (cDNA matching)
default: 18
-exdrop specify the Xdrop value for edit distance extension (cDNA
matching)
default: 2
-prminmatchlen specify minimum match length (protein matches)
default: 24
-prseedlength specify seed length (protein matching)
default: 10
-prhdist specify Hamming distance (protein matching)
default: 4
-gcmaxgapwidth set the maximum gap width for global chains
defines approximately the maximum intron length
set to 0 to allow for unlimited length
in order to avoid false-positive exons (lonely exons) at the
sequence ends, it is very important to set this parameter
appropriately!
default: 1000000
-gcmincoverage set the minimum coverage of global chains regarding to the
reference sequence
default: 50
-paralogs compute paralogous genes (different chaining procedure)
default: no
-introncutout enable the intron cutout technique
default: no
-fastdp use jump table to increase speed of DP calculation
default: no
-autointroncutout set the automatic intron cutout matrix size in megabytes and
enable the automatic intron cutout technique
default: 0
-intermediate stop after calculation of spliced alignments and output
results in reusable XML format. Do not process this output
yourself, use the ``normal'' XML output instead!
default: no
-first set the maximum number of spliced alignments per genomic DNA
input. Set to 0 for unlimited number.
default: 0
-help display help for basic options and exit
-help+ display help for all options and exit
-version display version information and exit
debian/rules
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f30ceda8
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@@ -10,6 +10,7 @@ export DEB_BUILD_MAINT_OPTIONS=hardening=+all
override_dh_clean:
dh_clean
rm -rf bin/bssm debian/bssm bin/gthdata debian/gthdata
rm -rf $(CURDIR)/debian/man
override_dh_auto_build:
make licensemanager=no opt=yes 64bit=yes
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@@ -26,7 +27,7 @@ ifeq (,$(filter nocheck,$(DEB_BUILD_OPTIONS)))
endif
override_dh_installman:
#
mkdir -p $(CURDIR)/debian/man
#
asciidoctor -a docdate='' -b manpage $(CURDIR)/debian/man_src/*.adoc
#
cp $(CURDIR)/debian/man_src/*.? $(CURDIR)/debian/man
mkdir -p $(CURDIR)/debian/man
asciidoctor -a docdate='' -b manpage $(CURDIR)/debian/man_src/*.adoc
cp $(CURDIR)/debian/man_src/*.? $(CURDIR)/debian/man
dh_installman --