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mapreads

    mapreads

    May 03, 2011

    Summary

    Mapreads is a ABI provided aligner for short length color space reads.

    Available on

    Fourierseq

    User documentation

    • To get started using mapreads, download mapreads manual.

    How to run mapreads

    Example command for running mapreads:

    mapreads in.csfasta ref.fasta A=1 M=3 L=35 I=1 S=0 T=/home/scott/coronalite/etc/schemas/schema_35_3 > out

    where

    in.csfasta : reads file (in color space)
    ref.fasta : reference genome (in base space)
    A=1 : count 2 consistent mismatches as 1 mismatch
    M=3: allow for 3 mismatches (in seed alone)
    L= 35 : length of read
    I= 1:  reference sequence is multiple sequences.
    S= 0: analyze in color space
    T= /home/scott/coronalite/etc/schemas/schema_35_3 : template file (for 35 length reads with 3 mismatches)
    
    , multiple selections available,

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    Bioinformatics Team (BioITeam) at the University of Texas
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    • Bioconductor
    • BioMart Perl APIs
    • Blast
    • BLAST tools
    • BOOST libraries
    • Bowtie
    • Breakdancer
    • BWA
    • BWA-SAMTOOLS workflow
    • CASAVA
    • Circos
    • CGView
    • Clustering programs - MCL and usearch, uclust
    • Conversion of gene ID's from one form to another (i.e. NCBI to Ensembl & vice-versa)
    • Conversion of mapreads output to GFF, SAM, or BAM format
    • Convert ABI SOLiD data to fasta fastq
    • Cufflinks
    • Data compression programs
    • Extracting barcode split data from SOLiD 5500 XSQ files
    • 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
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