view CSP2/CSP2_env/env-d9b9114564458d9d-741b3de822f2aaca6c6caa4325c4afce/opt/bbmap-39.01-1/cutgff.sh @ 69:33d812a61356

planemo upload commit 2e9511a184a1ca667c7be0c6321a36dc4e3d116d
author jpayne
date Tue, 18 Mar 2025 17:55:14 -0400
parents
children
line wrap: on
line source
#!/bin/bash

usage(){
echo "
Written by Brian Bushnell
Last modified October 15, 2019

Description:  Cuts out features defined by a gff file, and writes them
to a new fasta.  Features are output in their sense strand.

Usage:  cutgff.sh in=<fna file> gff=<gff file> out=<fna file>

in= is optional, and gff filenames will be automaitically assumed based on
the fasta name if not specified.  This allows running on multiple files
like this:

cutgff.sh types=rRNA out=16S.fa minlen=1440 maxlen=1620 attributes=16S bacteria/*.fna.gz


File Parameters:
in=<file>           Input FNA (fasta) file.
gff=<file>          Input GFF file (optional).
out=<file>          Output FNA file.

Other Parameters:
types=CDS           Types of features to cut.
invert=false        Invert selection: rather outputting the features,
                    mask them with Ns in the original sequences.
attributes=         A comma-delimited list of strings.  If present, one of
                    these strings must be in the gff line attributes.
bannedattributes=   A comma-delimited list of banned strings.
banpartial=t        Ignore lines with 'partial=true' in attributes.
minlen=1            Ignore lines shorter than this.
maxlen=2147483647   Ignore lines longer than this.
renamebytaxid=f     Rename sequences with their taxID.  Input sequences
                    must be named appropriately, e.g. in NCBI format.
taxmode=accession   Valid modes are:
                       accession: Sequence names must start with an accession.
                       gi:        Seqence names must start with gi|number
                       taxid:     Sequence names must start with tid|number
                       header:    Best effort for various header formats.
requirepresent=t    Crash if a taxID cannot be found for a sequence.
oneperfile=f        Only output one sequence per file.
align=f             Align ribosomal sequences to consensus (if available);
                    discard those with low identity, and flip those
                    annotated on the wrong strand.
maxns=-1            If non-negative, ignore features with more than this many
                    undefined bases (Ns or IUPAC symbols).
maxnfraction=-1.0   If non-negative, ignore features with more than this
                    fraction of undefined bases (Ns or IUPAC symbols).
                    Should be 0.0 to 1.0.
"
}

#This block allows symlinked shellscripts to correctly set classpath.
pushd . > /dev/null
DIR="${BASH_SOURCE[0]}"
while [ -h "$DIR" ]; do
  cd "$(dirname "$DIR")"
  DIR="$(readlink "$(basename "$DIR")")"
done
cd "$(dirname "$DIR")"
DIR="$(pwd)/"
popd > /dev/null

#DIR="$( cd "$( dirname "${BASH_SOURCE[0]}" )" && pwd )/"
CP="$DIR""current/"

z="-Xmx200m"
set=0

if [ -z "$1" ] || [[ $1 == -h ]] || [[ $1 == --help ]]; then
	usage
	exit
fi

calcXmx () {
	source "$DIR""/calcmem.sh"
	setEnvironment
	parseXmx "$@"
}
calcXmx "$@"

gff() {
	local CMD="java $EA $EOOM $z -cp $CP gff.CutGff $@"
#	echo $CMD >&2
	eval $CMD
}

gff "$@"