Statistics about the flags and reads in a BAM
Usage: bamstats02 [options] Files
Options:
-B, --bed
A source of intervals. The following suffixes are recognized: vcf,
vcf.gz bed, bed.gz, gtf, gff, gff.gz, gtf.gz.Otherwise it could be an
empty string (no interval) or a list of plain interval separated by '[
\t\n;,]'
-h, --help
print help and exit
--helpFormat
What kind of help. One of [usage,markdown,xml].
-o, --output
Output file. Optional . Default: stdout
-R, --ref
For reading/writing CRAM files. Indexed fasta Reference file. This file
must be indexed with samtools faidx and with picard
CreateSequenceDictionary
--version
print version and exit
${PATH}
. Setting JAVA_HOME is not enough : (e.g: https://github.com/lindenb/jvarkit/issues/23 )$ git clone "https://github.com/lindenb/jvarkit.git"
$ cd jvarkit
$ ./gradlew bamstats02
The java jar file will be installed in the dist
directory.
The project is licensed under the MIT license.
Should you cite bamstats02 ? https://github.com/mr-c/shouldacite/blob/master/should-I-cite-this-software.md
The current reference is:
http://dx.doi.org/10.6084/m9.figshare.1425030
Lindenbaum, Pierre (2015): JVarkit: java-based utilities for Bioinformatics. figshare. http://dx.doi.org/10.6084/m9.figshare.1425030
$ find dir -name "*final.bam" | xargs java -jar dist/bamstats02.jar -B capture.bed > output.tsv
$ verticalize output.tsv
>>> 2
$1 #filename dir/Sample0258.final.bam
$2 sampleName Sample0258
$3 chromosome 2
$4 mapq 60
$5 inTarget 1
$6 READ_PAIRED 1
$7 READ_MAPPED_IN_PROPER_PAIR 1
$8 READ_UNMAPPED 0
$9 MATE_UNMAPPED 0
$10 READ_REVERSE_STRAND 1
$11 MATE_REVERSE_STRAND 0
$12 FIRST_IN_PAIR 0
$13 SECOND_IN_PAIR 1
$14 NOT_PRIMARY_ALIGNMENT 0
$15 READ_FAILS_VENDOR_QUALITY_CHECK 0
$16 READ_IS_DUPLICATE 0
$17 SUPPLEMENTARY_ALIGNMENT 0
$18 count 463982
<<< 2
>>> 3
>>> 3
$1 #filename dir/Sample0258.final.bam
$2 sampleName Sample0258
$3 chromosome .
$4 mapq 0
$5 inTarget -1
$6 READ_PAIRED 1
$7 READ_MAPPED_IN_PROPER_PAIR 0
$8 READ_UNMAPPED 1
$9 MATE_UNMAPPED 1
$10 READ_REVERSE_STRAND 0
$11 MATE_REVERSE_STRAND 0
$12 FIRST_IN_PAIR 1
$13 SECOND_IN_PAIR 0
$14 NOT_PRIMARY_ALIGNMENT 0
$15 READ_FAILS_VENDOR_QUALITY_CHECK 0
$16 READ_IS_DUPLICATE 0
$17 SUPPLEMENTARY_ALIGNMENT 0
$18 count 458630
<<< 3
>>> 4
$1 #filename dir/Sample0258.final.bam
$2 sampleName Sample0258
$3 chromosome .
$4 mapq 0
$5 inTarget -1
$6 READ_PAIRED 1
$7 READ_MAPPED_IN_PROPER_PAIR 0
$8 READ_UNMAPPED 1
$9 MATE_UNMAPPED 1
$10 READ_REVERSE_STRAND 0
$11 MATE_REVERSE_STRAND 0
$12 FIRST_IN_PAIR 0
$13 SECOND_IN_PAIR 1
$14 SECONDARY_ALIGNMENT 0
$15 READ_FAILS_VENDOR_QUALITY_CHECK 0
$16 READ_IS_DUPLICATE 0
$17 SUPPLEMENTARY_ALIGNMENT 0
$18 count 458630
<<< 4
```
BamStats02View