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PHIM
RNAja-pipeline
Commits
dae2a622
Commit
dae2a622
authored
4 years ago
by
CamilleC
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Delete 01_Pipeline-Bulkrna_3D7.sh
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Scripts/01_Pipeline-Bulkrna_3D7.sh
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#!/bin/bash
GENERAL
=
/Users/COHEN/Documents/BulkRNA/AnalysesBioinformatiques/
GENOME
=
/Users/COHEN/Documents/BulkRNA/AnalysesBioinformatiques/02_Genome/PlasmoDB-46_Pfalciparum3D7_AnnotatedTranscripts.fasta
# rajouter a l'avenir les genes var référencés et enlever les genes vars de 3D7.
READS
=
//Users/COHEN/Documents/BulkRNA/AnalysesBioinformatiques/01_RawData
FASTQC
=
/usr/local/bin/fastqc
TRIMM
=
/Users/COHEN/Documents/Logiciels/trimmomatic-0.39/trimmomatic-0.39.jar
STAR
=
/Users/COHEN/Documents/Logiciels/star-2.7.3a/bin/macosx_x86_64/
PATH_DATA_TRIM
=
/Users/COHEN/Documents/BulkRNA/AnalysesBioinformatiques/04_Trimm
#---------------------------------------------------------------------------------------------------------------------------------------------
#FastQC
cd
$GENERAL
echo
"########################## FastQC ##########################"
if
[
!
-d
"03_FastQC"
]
;
then
#Creation du fichier
mkdir
-p
03_FastQC
#-p créer tous les dossiers dans l'aborescence
for
fq
in
$READS
/
*
_R1.fastq.gz
do
f2
=
${
fq
%%_R1.fastq.gz
}
"_R2.fastq.gz"
f3
=
${
fq
%%_*
}
echo
"We do FastQC for:"
$f3
"."
fastqc
-o
FastQC
-t
4
$f1
$f2
#-o repertoire output pour l'échantillon -t est le nombre de taches que lui dit de faire en mm temps 1 coeur= 1 tache
done
fi
#--------------------------------------------------------------------------------------------------------------------------------------------
#Trimming avec trimmomatic
echo
"########################### Trimming des séquences ##########################"
if
[
!
-d
"04_Trimm"
]
;
then
#Creation du fichier
mkdir
"04_Trimm"
cd
$READS
for
ft
in
*
_R1.fastq.gz
;
do
f1
=
$ft
f2
=
${
ft
/_R1.fastq.gz/
}
_R2.fastq.gz
f3
=
${
ft
%%_*
}
java
-jar
/Users/COHEN/Documents/Logiciels/trimmomatic-0.39/trimmomatic-0.39.jar PE
-trimlog
Resultslog.txt
$f1
$f2
$f3
"_1_paired.fq.gz"
$f3
"_1_unpaired.fq.gz"
$f3
"_2_paired.fq.gz"
$f3
"_2_unpaired.fq.gz"
ILLUMINACLIP:/Users/COHEN/Documents/Logiciels/trimmomatic-0.39/adapters/TruSeq3-PE-2.fa:2:30:10 LEADING:3 TRAILING:3 SLIDINGWINDOW:4:15 MINLEN:50
mv
$f3
"_1_paired.fq.gz"
$f3
"_1_unpaired.fq.gz"
$f3
"_2_paired.fq.gz"
$f3
"_2_unpaired.fq.gz"
/Users/COHEN/Documents/BulkRNA/AnalysesBioinformatiques/04_Trimm
done
fi
#--------------------------------------------------------------------------------------------------------------------------------------------
## /!\ DO NOT RUN /!\
#Indexing for STAR
cd
$GENERAL
if
[
!
-d
"05_Index_STAR"
]
;
then
echo
"########################### Indexing for STAR ##########################"
cd
/Users/COHEN/Documents/BulkRNA/AnalysesBioinformatiques/02_Genome/P0060623_1612/
mkdir
"05_Index_STAR"
cd
/Users/COHEN/Documents/BulkRNA/AnalysesBioinformatiques/
/Users/COHEN/Documents/Logiciels/STAR-2-7-5c/bin/MacOSX_x86_64/STAR
\
--runMode
genomeGenerate
\
--runThreadN
4
\
--genomeDir
/Users/COHEN/Documents/BulkRNA/AnalysesBioinformatiques/02_Genome/05_Index_STAR
\
--genomeFastaFiles
/Users/COHEN/Documents/BulkRNA/AnalysesBioinformatiques/02_Genome/plasmodb-46_pfalciparum3d7_genome.fasta
\
--sjdbGTFfile
/Users/COHEN/Documents/BulkRNA/AnalysesBioinformatiques/02_Genome/plasmodb-46_pfalciparum3d7_gffread.gtf
\
fi
cd
$GENERAL
#Mapping with STAR
if
[
!
-d
"05-Mapping_STAR"
]
;
then
echo
"########################### Mapping with STAR ##########################"
mkdir
"05-Mapping_STAR"
cd
$PATH_DATA_TRIM
for
f1
in
*
_1_paired.fq.gz
do
f2
=
${
f1
%%_1_paired.fq.gz
}
"_2_paired.fq.gz"
echo
$f2
f3
=
${
f1
%_1_paired.fq.gz
}
echo
$f3
echo
"We do the mapping for:"
$f3
"."
/Users/COHEN/Documents/Logiciels/STAR-2-7-5c/bin/MacOSX_x86_64/STAR
--runThreadN
4
\
--genomeDir
/Users/COHEN/Documents/BulkRNA/AnalysesBioinformatiques/02_Genome/05_Index_STAR
\
--readFilesIn
$f1
$f2
\
--readFilesCommand
gunzip
-c
\
--outFileNamePrefix
/Users/COHEN/Documents/BulkRNA/AnalysesBioinformatiques/05-Mapping_STAR/
"/"
$f3
\
--outSAMtype
BAM SortedByCoordinate
\
--sjdbGTFfile
/Users/COHEN/Documents/BulkRNA/AnalysesBioinformatiques/02_Genome/plasmodb-46_pfalciparum3d7_gffread.gtf
\
--sjdbGTFtagExonParentTranscript
Parent
\
--runMode
alignReads
\
--outFilterMultimapNmax
1
\
--outFilterMatchNmin
35
\
--twopassMode
Basic
done
fi
cd
\ No newline at end of file
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