File: removemicrobes.sh

package info (click to toggle)
bbmap 39.20%2Bdfsg-3
  • links: PTS, VCS
  • area: main
  • in suites: forky, sid
  • size: 26,024 kB
  • sloc: java: 312,743; sh: 18,099; python: 5,247; ansic: 2,074; perl: 96; makefile: 39; xml: 38
file content (81 lines) | stat: -rwxr-xr-x 2,947 bytes parent folder | download | duplicates (3)
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
76
77
78
79
80
81
#!/bin/bash

usage(){
echo "
Written by Brian Bushnell
Last modified December 22, 2021
This script requires at least 10GB RAM.
It is designed for NERSC and uses hard-coded paths.

Description:  Removes all reads that map to selected common microbial contaminant genomes.
Removes approximately 98.5% of common contaminant reads, with zero false-positives to non-bacteria.
NOTE!  This program uses hard-coded paths and will only run on Nersc systems.

Usage:  removemicrobes.sh in=<input file> outu=<clean output file>

Input may be fasta or fastq, compressed or uncompressed.

Parameters:
in=<file>           Input reads.  Should already be adapter-trimmed.
outu=<file>         Destination for clean reads.
outm=<file>         Optional destination for contaminant reads.
threads=auto        (t) Set number of threads to use; default is number of logical processors.
overwrite=t         (ow) Set to false to force the program to abort rather than overwrite an existing file.
interleaved=auto    (int) If true, forces fastq input to be paired and interleaved.
trim=t              Trim read ends to remove bases with quality below minq.
                    Values: t (trim both ends), f (neither end), r (right end only), l (left end only).
untrim=t            Undo the trimming after mapping.
minq=4              Trim quality threshold.
ziplevel=6          (zl) Set to 1 (lowest) through 9 (max) to change compression level; lower compression is faster.

build=1             Choses which masking mode was used:  
                    1 is most stringent and should be used for bacteria.
                    2 uses fewer bacteria for masking (only RefSeq references).
                    3 is only masked for plastids and entropy, for use on anything except bacteria.
                    4 is unmasked.

***** All BBMap parameters can be used; run bbmap.sh for more details. *****

Please contact Brian Bushnell at bbushnell@lbl.gov if you encounter any problems.
"
}

#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/"
JNI="-Djava.library.path=""$DIR""jni/"
JNI=""

z="-Xmx6000m"
z2="-Xms6000m"
set=0

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

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

function removemicrobes() {
	local CMD="java $EA $EOOM $z $z2 $JNI -cp $CP align2.BBMap strictmaxindel=4 bwr=0.16 bw=12 ef=0.001 minhits=2 path=/global/cfs/cdirs/bbtools/commonMicrobes pigz unpigz zl=6 qtrim=r trimq=10 untrim idtag printunmappedcount ztd=2 kfilter=25 maxsites=1 k=13 minid=0.95 idfilter=0.95 minhits=2 build=1 bloomfilter $@"
	echo $CMD >&2
	eval $CMD
}

removemicrobes "$@"