Results for "Single Nucleotide Polymorphisms"

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  • Murasaki

    Murasaki is an anchor alignment program that is exteremely fast (17 CPU hours for whole Hum...itrarily parallelizable across multiple nodes using MPI) memory efficient. (Even a single node w...

    2787 days ago

  • COSMIC

    The accurate description and annotation of structural variants can be complex.  This is d...n to the actual base pair positions. Furthermore, multiple rearrangements in a single area o...

    2786 days ago

  • ART: Set of Simulation Tools

    ART is a set of simulation tools to generate synthetic next-generation sequencing reads. ART s...ads using user own read error model or quality profiles. ART supports simulation of single-end, p...

    2753 days ago

  • HybPiper

    HybPiper was designed for targeted sequence capture, in which DNA sequencing libraries are enr...information, please see our wiki. HybPiper is run separately for each sample (single or pai...

    2753 days ago

  • RECORD

    Background. Next-generation sequencing technologies are now producing multiple times the genome size in total reads from a single experi...

    2731 days ago

  • bipype

    Bipype is a very useful program, which prepare a lot of types of bioinformatics analyses. Ther...SA coordinates of the input reads and generates alignments in the SAM format given single-end re...

    2725 days ago

  • fqtools

    fqtools is a software suite for fast processing of FASTQ files. Various file...Most of the individual subcommands will take either a single fil...ed. For subcommands that generate FASTQ data, either a single file o...

    2718 days ago

  • EAGER

    The automated reconstruction of genome sequences in ancient genome analysis is a multifaceted...each step as well as new complementary tools tailored for ancient DNA data within a single integr...

    2716 days ago

  • pyScaf

    pyScaf orders contigs from genome assemblies utilising several types of information: paired-end (PE) and/or mate-...f divergence between reference genome and assembled contigs is below 20% at nucleotide le...

    2707 days ago

  • MEME suite

    Motif based sequence analysis suits  The MEME Suite allows the biologist to discover novel motifs in collections of unaligned nucleotide or...

    2703 days ago