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SHRiMP

    SHRiMP

    Nov 19, 2013

    Summary

    SHRiMP is a an aligner from the University of Toronto which uses a vectored Smith-Waterman for alignment. Although it is slow, it detects alignments with high sensitivity and accuracy. It supports color space data.

    Available on

    Fourierseq - current version: 2.2.1 (updated 11/14/11).

    Phylocluster - version: 2.0

    User documentation

    • To get started using SHRiMP, read through the the SHRiMP documentation.

    How to run SHRiMP

    SHRiMP (rmapper) results can vary greatly based upon the input parameters. So please select parameters accordingly.

    The base commands on Fourierseq are:
    for color space:

    gmapper-cs
    

    and for base space:

    gmapper-ls
    

    The input parameters that we typically use with color space data are the following:

    gmapper-cs -p opp-in -N 4 -1 F3/V3BC17_RNA.csfasta -2 F5/V3BC17_RNA.csfasta /home/scott/Downloads/mouse.rna.fna > bc17.sam 2> bc17.log &
    

    Tip: To view the actual alignments in base space as part of the output file, add -p option (prettyprint).

    , multiple selections available,

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    • FastQC
    • Fastx Toolkit
    • Galaxy Setup
    • Geneid
    • General parser scripts
    • Generation of gene counts from results of mapping to genome
    • Generation of wig files from mapreads output
    • GeneWise
    • Genome Analysis Tool Kit
    • Getting an account on GSAF server-fourierseq
    • Get Tm (melting temperature), length, and %GC from a bunch of sequences
    • glimmer3
    • GMAP and GSNAP
    • Graphic programs
    • GS Amplicon variant analyzer
    • GS De novo assembler
    • GS Reference mapper
    • GS Run processor and run browser
    • Hmmer
    • IGV
    • Make a quick venn diagram based on lists in 3 files
    • mapreads
    • MAQ
    • MaqView
    • Median polish to consolidate quantitations
    • MegaMapper
    • MeV
    • MIRA
    • Mosaik
    • muscle
    • Phred, Phrap, Consed, cross_match, daev
    • Picard
    • Plot a read length histogram based on sequences in a fasta file
    • Python Library
    • Quick tips on GO analysis
    • R and R packages
    • Reverse complement for fasta files
    • RNA-seq workflow
    • SAMTOOLS
    • Sff file manipulation tools
    • SHRiMP
    • Small rna analysis
    • Small-rna data analysis
    • Small RNA Pipeline
    • SOAP
    • SOAPtrans
    • Tips for working with TACC resources
    • Tophat- Cufflinks
    • Tophat-Cufflinks-Cuffdiff, allowing for novel transcripts
    • Tophat-Cufflinks-Cuffdiff, ignoring novel transcripts
    • Tricks to preprocess SOLiD and 454 data
    • Trinity
    • Variant calling
    • Velvet
    • ZOHO Information
    • Removing duplicates from alignment output
    • SAMStat
    • TACC Lonestar workflow scripts
    • Get FASTQ Format
    • launcher_creator.py
    • Wrappers For TACC
    • ssh - generating keys
      Calendars

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