📅  最后修改于: 2023-12-03 14:59:30.895000             🧑  作者: Mango
Bedtools is a powerful suite of command line tools for dealing with genomic data. One of its most commonly used tools is bamToBed
, which converts BAM files into the BED format.
Bedtools can be installed using the following command:
$ conda install -c bioconda bedtools
The basic usage of bamToBed
is:
$ bedtools bamToBed -i input.bam > output.bed
This will take the BAM file input.bam
and convert it into the BED file output.bed
.
By default, bamToBed
will output the coordinates of each read in the BED format. For paired-end reads, it will output both the coordinates of the first read and the coordinates of the second read in separate rows.
There are several options that can be used with bamToBed
to modify its behavior:
-bed12
: output 12-column BED format, including block sizes and gaps for spliced alignments-split
: split reads with Ns in CIGAR into individual exons-mate1
, -mate2
: output only the first or second mate of paired-end reads-iout
, -iout_offset
: modify output coordinates by a fixed amountTo convert only the second mate of paired-end reads, use the -mate2
option:
$ bedtools bamToBed -mate2 -i input.bam > output.bed
To output the coordinates of each exon instead of the entire read, use the -split
option:
$ bedtools bamToBed -split -i input.bam > output.bed
To adjust the output coordinates by a fixed amount, use the -iout
and/or -iout_offset
options:
$ bedtools bamToBed -iout BEDPE -iout_offset 250 -i input.bam > output.bed
This will convert the BAM file into a BEDPE file (which includes both mates of a paired-end read in a single row), and will offset the coordinates by 250 base pairs.
bamToBed
is a useful tool for converting BAM files into the BED format. With its many options and advanced features, it can be customized to fit a wide variety of use cases.