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bioinfo
datautils
Commits
8a595336
Commit
8a595336
authored
10 years ago
by
Holger Brandl
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initial commit of dge workflow
parent
eb740601
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R/core_commons.R
+1
-0
1 addition, 0 deletions
R/core_commons.R
R/utils/spinr.R
+1
-12
1 addition, 12 deletions
R/utils/spinr.R
bash/lsf_rna_seq.sh
+0
-167
0 additions, 167 deletions
bash/lsf_rna_seq.sh
with
2 additions
and
179 deletions
R/core_commons.R
+
1
−
0
View file @
8a595336
...
...
@@ -190,6 +190,7 @@ rmerge <- function(LDF, by, ...){
trim_ext
<-
function
(
fileNames
,
...
)
trimEnd
(
fileNames
,
...
)
trimEnd
<-
function
(
fileNames
,
exts
=
c
()){
for
(
fileExt
in
exts
){
fileNames
<-
str_replace
(
fileNames
,
paste
(
fileExt
,
"$"
,
sep
=
""
),
""
)
...
...
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R/utils/spinr.R
+
1
−
12
View file @
8a595336
## a thin wrapper around spin to make it more useful with more custom output
require
(
knitr
)
require
(
stringr
)
...
...
@@ -7,14 +8,6 @@ options(width=150)
#https://groups.google.com/forum/#!topic/knitr/ojcnq5Nm298
## better table css: http://www.stat.ubc.ca/~jenny/STAT545A/topic10_tablesCSS.html
#setwd("/local/home/brandl/mnt/mack/project-raphael/reports/spin_report")
#setwd("/home/brandl/mnt/mack/project-raphael/reports/spin_report")
#rScript='/home/brandl/mnt/mack/project-raphael/Rcode/misc/DivisionPerpendicularity.R'
#rScript='/home/brandl/mnt/mack/project-raphael/Rcode/misc/Test.R'
#spinr <- function(rScript){
spin
(
rScript
,
knit
=
F
)
mdScript
<-
str_replace
(
rScript
,
"[.]R$"
,
".Rmd"
)
...
...
@@ -36,7 +29,3 @@ opts_chunk$set(cache = TRUE, fig.width=10, width=120)
knit2html
(
basename
(
mdScript
),
header
=
cssHeader
)
file.remove
(
basename
(
mdScript
))
#}
# spinr("/home/brandl/mnt/mack/project-raphael/Rcode/misc/DivisionPerpendicularity.R")
# spinr("/home/brandl/mnt/mack/project-raphael/Rcode/misc/Test.R")
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bash/lsf_rna_seq.sh
deleted
100644 → 0
+
0
−
167
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eb740601
## docs
## http://blog.joncairns.com/2013/08/what-you-need-to-know-about-bash-functions/
## create fastq report for all fastq and fastq.gz files in the current directory
dge_fastqc
(){
while
getopts
"o:"
curopt
;
do
case
$curopt
in
o
)
outputDir
=
$OPTARG
;
esac
done
shift
$((
$OPTIND
-
1
))
local
fastqFiles
=
$*
#if [ -z "$fastqFiles" ]; then
if
[
$#
-lt
1
]
;
then
echo
"Usage: dge_fastqc [-o <output_directory>] [<fastq.gz file>]+"
>
&2
;
return
;
fi
## use default directory if not specified
if
[
-z
"
$outputDir
"
]
;
then
outputDir
=
"fastqc_reports"
fi
if
[
!
-d
"
$outputDir
"
]
;
then
echo
"creating output directory '
$outputDir
'"
mkdir
$outputDir
fi
for
fastqFile
in
$fastqFiles
;
do
echo
"fastqcing
$fastqFile
"
if
[
!
-f
$fastqFile
]
;
then
continue
;
fi
mysub
"fastqc__
$(
basename
$fastqFile
)
"
"fastqc -j /sw/bin/java -o
$outputDir
-f fastq
$fastqFile
"
-q
medium | joblist .fastqc_jobs
done
wait4jobs .fastqc_jobs
mailme
"fastqc done for
$outputDir
"
# todo create some summary report here
}
export
-f
dge_fastqc
#http://wiki.bash-hackers.org/howto/getopts_tutorial
dge_tophat_se
(){
# http://stackoverflow.com/questions/18414054/bash-getopts-reading-optarg-for-optional-flags
echo
$*
while
getopts
"i:"
curopt
;
do
case
$curopt
in
i
)
IGENOME
=
"
$OPTARG
"
;
esac
done
shift
$((
$OPTIND
-
1
))
local
fastqFiles
=
$*
echo
fastq
$fastqFiles
echo
igenomes
"
$IGENOME
"
if
[
-z
"
$IGENOME
"
]
||
[
-z
"
$fastqFiles
"
]
;
then
echo
"Usage: dge_tophat_se -i <path to igenome> [<fastq.gz file>]+"
>
&2
;
return
;
fi
export
bowtie_gindex
=
"
$IGENOME
/Sequence/Bowtie2Index/genome"
export
gtfFile
=
"
$IGENOME
/Annotation/Genes/genes.gtf"
#head $gtfFile
if
[
!
-f
$gtfFile
]
;
then
>
&2
echo
"gtf '
$gtfFile
' does not exis"
;
return
;
fi
if
[
-z
"
$(
which tophat
)
"
]
;
then
>
&2
echo
"no tomcat binary in PATH"
;
return
;
fi
echo
"running tophat using igenome '
$IGENOME
' for the following files"
ll
$fastqFiles
#fastqFiles=$(ls $baseDir/treps_pooled/*fastq.gz)
for
fastqFile
in
$fastqFiles
;
do
echo
"submitting tophat job for
$fastqFile
"
# DEBUG fastqFile=/projects/bioinfo/holger/projects/eric/trimmed/a1_ca.fastq.gz
fastqBaseName
=
$(
basename
${
fastqFile
%%.fastq.gz
}
)
outputdir
=
$fastqBaseName
## uniquely mapping reads only: http:/seqanswers.com/forums/showthread.php?s=93da11109ae12a773a128a637d69defe&t=3464
mysub
"
${
project
}
__tophat__
${
fastqBaseName
}
"
"
tophat -p6 -G
$gtfFile
-g1 -o
$outputdir
$bowtie_gindex
$fastqFile
mv
$outputdir
/accepted_hits.bam
$outputdir
/
$(
basename
$outputdir
)
.bam
samtools index
$outputdir
/
$(
basename
$outputdir
)
.bam
"
-n
5
-R
span[hosts
=
1]
-q
long | joblist .tophatjobs
done
wait4jobs .tophatjobs
## create tophat mapping report
source
<
(
curl https://dl.dropboxusercontent.com/u/113630701/datautils/bash/bioinfo_utils.sh 2>&1 2>/dev/null
)
TophatMappingReport
}
export
-f
dge_tophat_se
# dge_tophat_se
# dge_tophat_se -i
dge_cuffdiff
(){
local
gtfFile
=
$1
local
bamDir
=
$2
local
labels
=
$3
if
[
$#
-ne
3
]
;
then
echo
"Usage: dge_fastqc <gtf_file> <bam directory> <labels>"
>
&2
;
return
;
fi
if
[
-z
"
$(
which cuffdiff
)
"
]
;
then
>
&2
echo
"no cuffdiff binary in PATH"
;
return
;
fi
if
[
!
-f
$gtfFile
]
;
then
>
&2
echo
"gtf '
$gtfFile
' does not exis"
;
return
;
fi
## collect all bam-files and group them
allBams
=
$(
find
$bamDir
|
grep
".bam$"
|
grep
-v
"unmapped"
|
sort
)
bamsSplit
=
""
for
label
in
$(
echo
$labels
|
tr
", "
" "
)
;
do
echo
$label
labelBams
=
$(
echo
"
$allBams
"
|
grep
$label
| xargs
echo
-n
|
tr
' '
','
)
bamsSplit+
=
$labelBams
" "
done
#echo $bamsSplit
## make sure (again that all files are there
echo
$gtfFile
$bamsSplit
|
tr
","
" "
| xargs
ls
-la
#mysub ${project}_cuffdiff "cuffdiff -L aRGm,aRGp,aRG,bRG,IPC,N -o . -p 8 mm10_ensGene_ccds.gtf $amBams $apBams $aBams $bBams $cBams $dBams 2>&1 | tee cuffdiff.log" -q long -n 8 -R span[hosts=1] | blockScript
cdCmd
=
"cuffdiff -L
$labels
-o . -p 10
$gtfFile
$bamsSplit
"
#echo "cmd is: $cdCmd"
mysub
${
project
}
__cuffdiff
"
$cdCmd
"
-q
long
-n
8
-R
span[hosts
=
1] | blockScript
MakeCuffDB
$gtfFile
"NAN"
}
\ No newline at end of file
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