Results for "Alignment"

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  • kSNP3.0: SNP detection and phylogenetic analysis of genomes without genome alignment or reference genome

    Sept. 20, 2017 Version 3.1 released. Major upgrade. Version 3.1 fixes the problems with SNP annotation that arose when NCBI discontinued use of GI numbers. Please read carefully the Preface (page 3) and the File of annotated genomes section (pages 9-10) in the version 3.1 User Guide. Thanks to To...

    Tags: kSNP3.0, SNP, detection, phylogenetic, analysis, genomes, alignment, reference, genome

    2332 days ago

  • Mugsy: multiple whole genome alignment tool

    Mugsy is a multiple whole genome aligner. Mugsy uses Nucmer for pairwise alignment, a custom graph based segmentation procedure for identifying collinear regions, and the segment-based progressive multiple alignment strategy from Seqan::TCoffee. Mugsy accepts draft genomes in the form of multi-FA...

    Tags: Mugsy, multiple, whole, genome, alignment, tool

    2332 days ago

  • zPicture: A dynamic blastz alignment visualization

    zPicture is a dynamic alignment and visualization tool that is based on blastz alignment program utilized by PipMaker. zPicture alignments can be automatically submitted to rVista 2.0 to identify conserved transcription factor binding sites.

    Tags: zPicture, dynamic, blastz, alignment, visualization

    2279 days ago

  • xmatchview: smith-waterman alignment visualization

    xmatchview and xmatchview-conifer are imaging tools for comparing the synteny between DNA sequences. It allows users to align 2 DNA sequences in fasta format using cross_match and displays the alignment in a variety of image formats. xmatchview and xmatchview-conifer are written in python and run...

    Tags: xmatchview, smith-waterman, alignment, visualization, synteny

    2313 days ago

  • MUMmer4: A fast and versatile genome alignment system

    MUMmer4, a substantially improved version of MUMmer that addresses genome size constraints by changing the 32-bit suffix tree data structure at the core of MUMmer to a 48-bit suffix array, and that offers improved speed through parallel processing of input query sequences. With a theoretical limi...

    Tags: MUMmer4, fast, versatile, genome, alignment, system

    2276 days ago

  • HISAT2: a fast and sensitive alignment program for mapping next-generation sequencing reads

    HISAT2 is a fast and sensitive alignment program for mapping next-generation sequencing reads (both DNA and RNA) to a population of human genomes (as well as to a single reference genome). Based on an extension of BWT for graphs [Sirén et al. 2014], we designed and implemented a ...

    Tags: HISAT2, fast, sensitive, alignment, program, mapping, next-generation, sequencing, reads, tools

    2182 days ago

  • LAMSA: fast split read alignment with long approximate matches

    LAMSA (Long Approximate Matches-based Split Aligner) is a novel split alignment approach with faster speed and good ability of handling SV events. It is well-suited to align long reads (over thousands of base-pairs). LAMSA takes takes the advantage of the rareness of SVs to implement a specifi...

    Tags: LAMSA, fast, split, read, alignment, long, approximate, matches

    2175 days ago

  • minialign: fast and accurate alignment tool for PacBio and Nanopore long reads

    Minialign is a little bit fast and moderately accurate nucleotide sequence alignment tool designed for PacBio and Nanopore long reads. It is built on three key algorithms, minimizer-based index of the minimap overlapper, array-based seed chaining, and SIMD-parallel Smith-Waterman-Gotoh extension.

    Tags: minialign, fast, accurate, alignment, tool, PacBio, Nanopore, long, reads

    2166 days ago

  • GenomeMapper: Simultaneous alignment of short reads against multiple genomes

    GenomeMapper is a short read mapping tool designed for accurate read alignments. It quickly aligns millions of reads either with ungapped or gapped alignments. It can be used to align against multiple genomes simulanteously or against a single reference. If you are unsure which one is the appropr...

    Tags: GenomeMapper, Simultaneous, alignment, short, reads, multiple, genomes

    2165 days ago

  • Gblocks: eliminates poorly aligned positions and divergent regions of a DNA or protein alignment

    Gblocks eliminates poorly aligned positions and divergent regions of a DNA or protein alignment so that it becomes more suitable for phylogenetic analysis. This server implements the most important features of the Gblocks program to make its use as simple as possible without loosing the func...

    Tags: Gblocks, eliminates, poorly, aligned, positions, divergent, regions, DNA, protein, alignment

    2157 days ago