Results for "discordant read pairs"

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  • Smash: An alignment-free method to find and visualise rearrangements between pairs of DNA sequences

    Smash is a completely alignment-free method/tool to find and visualise genomic rearrangements. The detection is based on conditional exclusive compression, namely...

    2945 days ago

  • segemehl

    segemehl is a software to map short sequencer reads to reference genomes. Unlike other methods, sege...urthermore, segemehl is not limited to a specific read length and is able to map primer- or polyadenylation contaminated reads...

    2931 days ago

  • cutadapt

    Cutadapt finds and removes adapter sequences, primers, poly-A tails and other...uence from your high-throughput sequencing reads. Cleaning your data in this way is often required: Reads from small-RNA sequencing co...en you don’t want them to be in your reads...

    2928 days ago

  • Hagfish - assess an assembly through creative use of coverage plots

    Hagfish is a tool that is to be used in data analysis of Next Generation Sequencing (NGS) experiments. Hagfish bui...e of the paired end library is. Quick links: Installation,Operation, Read...

    2921 days ago

  • MOSAIK: A Hash-Based Algorithm for Accurate Next-Generation Sequencing Short-Read Mapping

    MOSAIK is a stable, sensitive and open-source program for mapping second and third-generation sequencing reads to a reference genome. Uniquely among current mapping tools, MOSAIK can align reads...

    2921 days ago

  • Blobology

    Tools for making blobplots or Taxon-Annotated-GC-Coverage plots (TAGC plots) to visualise the contents of genome a...e paper to create a preliminary assembly, and to create and collate GC content, read...

    2897 days ago

  • GAEMR

    The Genome Assembly Evaluation Metrics and Reporting (GAEMR) package is an assembly analy...specific charts and tables. GAEMR standardizes input by converting a variety of read...

    2896 days ago

  • CovCal: Coverage / Read Count Calculator

    Coverage / Read Count Calculator Calculate how much sequencing you need to hit a targ...of coverage (or vice versa). Instructions: set the read length/configuration and geno...ames Hadfield. Coverage is calculated as C=LN/G and reads...

    2180 days ago

  • WgSim

    Reads simulator Wgsim is a small tool for simulating sequence reads from a reference genome. It is able to simula...n/deletion (INDEL) polymorphisms, and simulate reads with uniform substitution se...e simulated polymorphisms, and writes the true read...

    2887 days ago

  • SAM flags

    Decoding SAM flags This utility makes it easy to identify what are the properties of a read based on its SAM flag value, or conversely, to find what the SAM Flag value would be for a given combin...

    2881 days ago