Eric Coissac
d4da1d01fd
clusterizecore.sh script from the detectors/cds/lib folder. The CDS detector is now modified to use the clean.fst files. Former-commit-id: e30a53b5b6b658388af4b2640b30e6765c729894 Former-commit-id: 3015ad50d25248fb117ab00e816b00fde1f9ba1d
323 lines
8.9 KiB
Bash
Executable File
323 lines
8.9 KiB
Bash
Executable File
#!/bin/bash
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#
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#
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#
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# Annotate Organelle
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#
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#========================================================================================
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#
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#
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#========================================================================================
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# -- CAUTION -- Works as long as the script
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# is not called through a symlink
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THIS_DIR="$(dirname ${BASH_SOURCE[0]})"
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source "${THIS_DIR}/scripts/bash_init.sh"
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#
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# Management of options
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#
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taxid="no"
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normalization="yes"
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irdetection="yes"
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organism="no"
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types="chloro"
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partial=0
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function usage {
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echo "Usage:" ;
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echo " $1 "'[-t|--ncbi-taxid ###] [-n|--no-normalization] \'
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echo ' [-i|--no-ir-detection] [-h|--help] \ '
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echo ' [-o|--organism <organism_name>] \ '
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echo ' [-c|--chloroplast|-r|--nuclear-rdna|-m|--mitochondrion] <FASTAFILE>'
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echo
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echo "Options:"
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echo ' -t ### | --ncbi-taxid ###'
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echo ' ### represents the ncbi taxid associated to the sequence'
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echo
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echo ' -i | --no-ir-detection'
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echo ' Does not look for inverted repeats in the plastid genome'
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echo
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echo ' -o | --organism <organism_name>'
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echo ' Allows for specifiying the organism name in the embl generated file'
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echo ' Spaces have to be substituted by underscore ex : Abies_alba'
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echo
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echo ' -c | --chloroplast'
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echo ' Selects for the annotation of a chloroplast genome'
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echo ' This is the default mode'
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echo
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echo ' -r | --nuclear-rdna'
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echo ' Selects for the annotation of the rDNA nuclear cistron'
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echo
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echo ' -m | --mitochondrion'
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echo ' Selects for the annotation of an animal mitochondrion genome'
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echo
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echo ' -p | --partial'
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echo ' Indicates that the genome sequence is partial and therefore in several contigs'
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exit $2
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}
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function fastaIterator() {
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awk '/^>/ {if (seq) printf("%s\f",seq); seq=""} \
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{if (seq) seq=seq"\n"; seq=seq $1} \
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END {print seq}' "$1"
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}
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# options may be followed by one colon to indicate they have a required argument
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if ! options=$(getopt -o t:o:icrmhp -l ncbi-taxid:,organism,no-ir-detection,chloroplast,nuclear-rdna,mitochondrion,partial,help -- "$@")
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then
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# something went wrong, getopt will put out an error message for us
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usage $0 1
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fi
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eval set -- "$options"
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while [ $# -gt 0 ]
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do
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case $1 in
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-t|--ncbi-taxid) taxid="$2" ; shift ;;
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-i|--no-ir-detection) irdetection="no" ;;
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-o|--organism) organism="$2" ; shift ;;
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-c|--chloroplast) types="chloro" ;;
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-r|--nuclear-rdna) types="nucrdna" ;;
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-m|--mitochondrion) types="mito" ;;
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-p|--partial) partial="1" ;;
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-h|--help) usage $0 0;;
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(--) shift; break;;
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(-*) echo "$0: error - unrecognized option $1" 1>&2; exit 1;;
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(*) break;;
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esac
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shift
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done
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#############################
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pushTmpDir ORG.organnot
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if [[ ! "$1" =~ ^/ ]]; then
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QUERY="${CALL_DIR}/$1"
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else
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QUERY="$1"
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fi
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RESULTS=$(basename ${QUERY/.*/})
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LOG="${CALL_DIR}/${RESULTS}.log"
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rm -f ${LOG}
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openLogFile ${LOG}
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IFS=$'\f'
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for sequence in $(fastaIterator "${QUERY}") ; do
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unset IFS
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if [[ ! -z "${sequence}" ]] ; then
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echo "${sequence}" > toannotate.fasta
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seqid=$(awk '(NR==1) {print substr($1,2,1000)}' toannotate.fasta)
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case "$types" in
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chloro)
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loginfo "Annotating a plant chloroplast genome..."
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if [[ "$irdetection"=="yes" ]] && (( partial == 0 )) ; then
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loginfo "Normalizing the structure of the Chloroplast sequence..."
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loginfo " LSC + IRB + SSC + IRA"
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${PROG_DIR}/detectors/normalize/bin/go_normalize.sh toannotate.fasta > "${RESULTS}.norm.fasta"
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loginfo "Done."
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loginfo "Annotating the Inverted repeats and Single copies (LSC and SSC)..."
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${PROG_DIR}/detectors/ir/bin/go_ir.sh "${RESULTS}.norm.fasta" > "${RESULTS}.annot"
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loginfo "Done."
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else
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cat toannotate.fasta > "${RESULTS}.norm.fasta"
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rm -f "${RESULTS}.annot"
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touch "${RESULTS}.annot"
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fi
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loginfo "Annotating the tRNA..."
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${PROG_DIR}/detectors/trna/bin/go_trna.sh "${RESULTS}.norm.fasta" >> "${RESULTS}.annot"
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loginfo "Done."
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loginfo "Annotating the rRNA genes..."
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${PROG_DIR}/detectors/rrna/bin/go_rrna.sh "${RESULTS}.norm.fasta" >> "${RESULTS}.annot"
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loginfo "Done."
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loginfo "Annotating the CDS..."
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tcsh -f ${PROG_DIR}/detectors/cds/bin/go_cds.csh "${RESULTS}.norm.fasta" >> "${RESULTS}.annot"
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loginfo "Done."
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if (( partial == 0 )) ; then
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topology="circular"
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defline="plastid, complete genome"
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else
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topology="linear"
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defline="plastid, partial sequence"
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fi
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;;
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nucrdna)
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loginfo "Annotating a plant rDNA cistron..."
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loginfo "Normalizing the structure of the cistron sequence..."
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${PROG_DIR}/detectors/normalizerdna/bin/go_normalizerdna.sh toannotate.fasta > "${RESULTS}.norm.fasta"
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loginfo "Done."
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loginfo "Annotating the rRNA genes..."
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${PROG_DIR}/detectors/nucrrna/bin/go_nucrrna.sh "${RESULTS}.norm.fasta" > "${RESULTS}.annot"
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loginfo "Done."
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topology="linear"
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defline="18S rRNA gene, ITS1, 5.8S rRNA gene, ITS2 and 28S rRNA gene"
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;;
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mito)
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loginfo "Annotating an animal mitochondrial genome..."
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logerror "Not yet implemented"
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if (( partial == 0 )) ; then
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topology="circular"
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defline="mitochondrion, complete genome"
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else
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topology="linear"
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defline="mitochondrion, partial sequence"
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fi
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exit 1
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;;
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*)
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usage $0 1;;
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esac
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if [[ "${organism}" == "no" ]]; then
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organism="{organism}"
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else
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organism="$(echo ${organism} | tr '_' ' ')"
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fi
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sl=$(seqlength "${RESULTS}.norm.fasta")
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loginfo "Printing minimal header..."
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echo "ID ${seqid}; ${seqid}; ${topology}; genomic DNA; XXX; XXX; ${sl} BP."
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echo "XX"
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echo "AC ${seqid};"
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echo "DE ${organism} ${defline}."
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echo "XX"
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loginfo "Done."
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loginfo "Printing annotations header..."
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echo "FH Key Location/Qualifiers"
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loginfo "Done."
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loginfo "Printing the source feature"
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echo "FT source 1..${sl}" >> "${RESULTS}.annot"
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if [[ "${organism}" != "{organism}" ]] ; then
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echo "FT /organism=\"${organism}\"" >> "${RESULTS}.annot"
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fi
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case "${types}" in
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chloro)
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echo "FT /organelle=\"plastid:chloroplast\"" >> "${RESULTS}.annot"
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;;
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mito)
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echo "FT /organelle=\"mitochondrion\"" >> "${RESULTS}.annot"
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;;
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*)
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loginfo "Nuclear sequence"
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;;
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esac
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echo "FT /mol_type=\"genomic DNA\"" >> "${RESULTS}.annot"
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if [[ "${taxid}" != "no" ]] ; then
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echo "FT /db_xref=\"taxon:${taxid}\"" >> "${RESULTS}.annot"
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fi
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# echo "FT /country=\"Poland: Bialowieza Forest\"" >> "${RESULTS}.annot"
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loginfo "Done."
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loginfo "Ordering annotations..."
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awk '/^.....(misc|repeat|rRNA|tRNA|gene|source)/ { \
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match($3,"[0-9][0-9]*"); \
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pos=substr($3,RSTART,RLENGTH)*1000 + 1; \
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print pos,$0; \
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next} \
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{ pos++; \
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print pos,$0}' "${RESULTS}.annot" | \
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sort -nk1 |\
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awk '{ \
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match($0,"^[0-9]* ");\
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line=substr($0,RLENGTH+1);\
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print line}'
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loginfo "Done."
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loginfo "Closing annotations table..."
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echo "XX"
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loginfo "Done."
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loginfo "Computing statistics on nucleotide usage..."
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awk '! /^>/ { \
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seq=toupper($0); \
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gsub(" ","",seq); \
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lseq=length(seq); \
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for (i=0; i < lseq; i++) { \
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freq[substr(seq,i,1)]++}\
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} \
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END { \
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other=0; \
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for (i in freq) { \
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if (i!="A" && i!="C" && i!="G" && i!="T") {\
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other+=freq[i] \
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} \
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}; \
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print "SQ Sequence "\
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(freq["A"]+freq["C"]+freq["G"]+freq["T"]+other) \
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" BP; "\
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freq["A"]" A; "\
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freq["C"]" C; "\
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freq["G"]" G; "\
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freq["T"]" T; "\
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other" other;" \
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}' "${RESULTS}.norm.fasta"
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loginfo "Done."
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loginfo "Reformating sequences..."
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lines=$(wc -l "${RESULTS}.norm.fasta" | awk '{print $1}')
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awk -v lines=$lines ' \
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! /^>/ { \
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seq=tolower($0); \
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gsub(" ","",seq); \
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printf(" ") ;\
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for (i=0; i < 6; i++) { \
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f=substr(seq,i * 10, 10); \
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pos+=length(f); \
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f = f substr(" ",1,10-length(f)); \
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printf("%s ",f) \
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}; \
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if (NR==lines) \
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{pos-=1}; \
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printf(" %6d\n",pos) \
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}' "${RESULTS}.norm.fasta"
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loginfo "Done."
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loginfo "Closing sequence part..."
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echo "//"
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loginfo "Done."
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fi
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IFS=$'\f'
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done # End of the loop over the sequences
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popTmpDir
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