Repository revision
Select a revision to inspect and download versions of Galaxy utilities from this repository.

Repository picard
Name: picard
Owner: devteam
Synopsis: Picard SAM/BAM manipulation tools.
SAM (Sequence Alignment/Map) is a generic format for storing large
nucleotide sequence alignments. Picard comprises Java-based utilities that manipulate
SAM files, and a Java API (SAM-JDK) for creating new programs that read and write
SAM files. Both SAM text format and SAM binary (BAM) format are supported.
Clone this repository: hg clone https://toolshed.g2.bx.psu.edu/repos/devteam/picard
Type: unrestricted
Revision: 17:fc288950c3b7
This revision can be installed: True
Times cloned / installed: 18390

Contents of this repository

Name Description Version Minimum Galaxy Version
convert coordinate data into picard interval list format 2.7.1.0 any
assess validity of SAM/BAM dataset 2.7.1.0 any
convert Fastq data into unaligned BAM 2.7.1.0 any
collect metrics about the alignment of RNA to various functional classes of loci in the genome 2.7.1.1 any
Downsample a file to retain a subset of the reads 2.7.1.0 any
chart quality score distribution 2.7.1.0 any
ensure that all mate-pair information is in sync between each read and it's mate pair 2.7.1.0 any
sort SAM/BAM dataset 2.7.1.1 any
compute metrics for evaluating of whole genome sequencing experiments 2.7.1.0 any
charts the nucleotide distribution per cycle in a SAM or BAM dataset 2.7.1.0 any
chart distribution of base qualities 2.7.1.0 any
charts the GC bias metrics 2.7.1.0 any
merges multiple SAM/BAM datasets into one 2.7.1.0 any
plots distribution of insert sizes 2.7.1.0 any
merge alignment data with additional info stored in an unmapped BAM dataset 2.7.1.0 any
perform SAM/BAM grooming 2.7.1.0 any
assess sequence library complexity from read sequences 2.7.1.0 any
examine aligned records in BAM datasets to locate duplicate molecules 2.7.1.0 any
examine aligned records in BAM datasets to locate duplicate molecules 2.7.1.1 any
add or replaces read group information 2.7.1.0 any
add comments to BAM dataset 2.7.1.0 any
extract reads and qualities from SAM/BAM dataset and convert to fastq 2.7.1.0 any
normalize fasta datasets 2.7.1.0 any
revert the original base qualities and add the mate cigar tag 2.7.1.0 any
revert SAM/BAM datasets to a previous state 2.7.1.0 any
include or exclude aligned and unaligned reads and read lists 2.7.1.0 any
reorder reads to match ordering in reference sequences 2.7.1.0 any
replace header in a SAM/BAM dataset 2.7.1.0 any
writes a file containing summary alignment metrics 2.7.1.1 any

Categories
SAM - Tools for manipulating alignments in the SAM format