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Repository bedtools
Name: bedtools
Owner: iuc
Synopsis: bedtools is a powerful toolset for genome arithmetic
Collectively, the bedtools utilities are a swiss-army knife of
tools for a wide-range of genomics analysis tasks. The most widely-used tools enable
genome arithmetic: that is, set theory on the genome. For example, bedtools allows
one to intersect, merge, count, complement, and shuffle genomic intervals from multiple
files in widely-used genomic file formats such as BAM, BED, GFF/GTF, VCF. While
each individual tool is designed to do a relatively simple task (e.g., intersect
two interval files), quite sophisticated analyses can be conducted by combining
multiple bedtools operations.
Clone this repository: hg clone https://toolshed.g2.bx.psu.edu/repos/iuc/bedtools
Type: unrestricted
Revision: 6:d25966c8ddeb
This revision can be installed: True
Times cloned / installed: 22392
Dependencies of this repository

Repository package_ncurses_5_9 revision 335ebf512407 owned by iuc (prior install required)
Repository package_zlib_1_2_8 revision 411985b46ae8 owned by iuc (prior install required)
Repository package_bedtools_2_24 revision 3416a1d4a582 owned by iuc

Name Version Type
bedtools 2.24 package
samtools 1.2 package

Contents of this repository

Name Description Version Minimum Galaxy Version
order the intervals 2.24.0 16.01
counts coverage from multiple BAMs at specific intervals 2.24.0 16.01
converter 2.24.0 16.01
annotate coverage of features from multiple files 2.24.1 16.01
create a HTML page of links to UCSC locations 2.24.0 16.01
calculate the distribution of relative distances between two files 2.24.0 16.01
make interval windows across a genome 2.24.0 16.01
converter 2.24.0 16.01
randomly redistrubute intervals in a genome 2.24.0 16.01
computes the amount of overlap from two intervals 2.24.0 16.01
find overlapping intervals in various ways 2.24.0 16.01
profile the nucleotide content of intervals in a FASTA file 2.24.0 16.01
combine overlapping/nearby intervals into a single interval 2.24.1 16.01
replicate lines based on lists of values in columns 2.24.0 16.01
generate random intervals in a genome 2.24.0 16.01
of features in file B on the features in file A (bedtools coverage) 2.24.1 16.01
converter 2.24.0 16.01
use intervals to mask sequences from a FASTA file 2.24.0 16.01
calculate the distribution of relative distances 2.24.0 16.01
tag BAM alignments based on overlaps with interval files 2.24.0 16.01
converter 2.24.0 16.01
2.24.0 16.01
use intervals to extract sequences from a FASTA file 2.24.0 16.01
combines coverage intervals from multiple BEDGRAPH files 2.24.0 16.01
identifies common intervals among multiple interval files 2.24.0 16.01
reports the distances between features 2.24.0 16.01
compute the coverage over an entire genome 2.24.0 16.01
calculate Fisher statistic between two feature files 2.24.0 16.01
cluster overlapping/nearby intervals 2.24.0 16.01
find overlapping intervals within a window around an interval 2.24.0 16.01
remove intervals based on overlaps 2.24.0 16.01
Extract intervals not represented by an interval file 2.24.0 16.01
find the closest, potentially non-overlapping interval 2.24.0 16.01
create new intervals from the flanks of existing intervals 2.24.0 16.01
apply a function to a column for each overlapping interval 2.24.1 16.01
adjust the size of intervals 2.24.0 16.01
group by common cols and summarize other cols 2.24.0 16.01

Categories
Text Manipulation - Tools for manipulating data
Genomic Interval Operations - Tools for operating on genomic intervals