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Repository rseqc
Name: rseqc
Owner: nilesh
Synopsis: an RNA-seq quality control package
RSeQC package provides a number of useful modules that can comprehensively
evaluate high throughput sequence data especially RNA-seq data. Some basic
modules quickly inspect sequence quality, nucleotide composition bias, PCR
bias and GC bias, while RNA-seq specific modules evaluate sequencing
saturation, mapped reads distribution, coverage uniformity, strand
specificity, transcript level RNA integrity etc.
Clone this repository: hg clone https://toolshed.g2.bx.psu.edu/repos/nilesh/rseqc
Type: unrestricted
Revision: 59:dbedfc5f5a3c
This revision can be installed: True
Times cloned / installed: 5477

Contents of this repository

Name Description Version Minimum Galaxy Version
estimates clipping profile of RNA-seq reads from BAM or SAM file 2.6.4 16.01
calculates the fragment size for each gene/transcript 2.6.4.1 16.01
calculate the inner distance (or insert size) between two paired RNA reads 2.6.4.1 16.01
Read coverage over gene body 2.6.4.3 16.01
determines reads duplication rate with sequence-based and mapping-based strategies 2.6.4 16.01
converts all types of RNA-seq data from .bam to .wig 2.6.4 16.01
Read coverage over gene body 2.6.4.2 16.01
calculates how mapped reads were distributed over genome feature 2.6.4.1 16.01
calculates hexamer (6mer) frequency for reads, genomes, and mRNA sequences 2.6.4 16.01
calculates raw count and RPKM values for transcript at exon, intron, and mRNA level 2.6.4.2 16.01
to check the nucleotide composition bias 2.6.4 16.01
calculates the distribution of mismatches across reads 2.6.4 16.01
speculates how RNA-seq were configured 2.6.4.1 16.01
detects splice junctions from each subset and compares them to reference gene model 2.6.4.1 16.01
calculates raw read count, FPM, and FPKM for each gene 2.6.4.1 16.01
determines Phred quality score 2.6.4 16.01
compares detected splice junctions to reference gene model 2.6.4.1 16.01
reads mapping statistics for a provided BAM or SAM file. 2.6.4 16.01
calculates the distributions of deleted nucleotides across reads 2.6.4 16.01
determines GC% and read count 2.6.4 16.01
calculates the distribution of inserted nucleotides across reads 2.6.4 16.01
evaluates RNA integrity at a transcript level 2.6.4.1 16.01

Categories
Convert Formats - Tools for converting data formats
Sequence Analysis - Tools for performing Protein and DNA/RNA analysis
Visualization - Tools for visualizing data