BamTools
BamTools provides both a programmer's API and an end-user's toolkit for handling BAM files.
Availability and Restrictions
Versions
The following versions of BamTools are available on OSC clusters:
BamTools provides both a programmer's API and an end-user's toolkit for handling BAM files.
The following versions of BamTools are available on OSC clusters:
STAR: Spliced Transcripts Alignment to a Reference.
The following versions of STAR are available on OSC clusters:
Trimmomatic performs a variety of useful trimming tasks for illumina paired-end and single ended data.The selection of trimming steps and their associated parameters are supplied on the command line.
The following versions of Trimmomatic are available on OSC clusters:
bam2fastq is used to extract raw sequences (with qualities) from programs like SAMtools, Picard, and Bamtools.
The following versions of bam2fastq are available on OSC clusters:
SnpEff is a variant annotation and effect prediction tool. It annotates and predicts the effects of variants on genes (such as amino acid changes).
The following versions of SnpEff are available on OSC clusters:
The Sequence Read Archive (SRA Toolkit) stores raw sequence data from "next-generation" sequencing technologies including 454, IonTorrent, Illumina, SOLiD, Helicos and Complete Genomics. In addition to raw sequence data, SRA now stores alignment information in the form of read placements on a reference sequence. Use SRA Toolkit tools to directly operate on SRA runs.
The following versions of SRA Toolkit are available on OSC clusters:
Ncview is a visual browser for netCDF format files. Typically you would use ncview to get a quick and easy, push-button look at your netCDF files. You can view simple movies of the data, view along various dimensions, take a look at the actual data values, change color maps, invert the data, etc.
The following versions of Ncview are available on OSC clusters:
The Subread package comprises a suite of software programs for processing next-gen sequencing read data like Subread, Subjunc, featureCounts, and exactSNP.
The following versions of Subread are available on OSC clusters:
VCFtools is a program package designed for working with VCF files, such as those generated by the 1000 Genomes Project. The aim of VCFtools is to provide easily accessible methods for working with complex genetic variation data in the form of VCF files.
The following versions of VCFtools are available on OSC clusters:
BCFtools is a set of utilities that manipulate variant calls in the Variant Call Format (VCF) and its binary counterpart BCF.
The following versions of BCFtools are available on OSC clusters: