Results for "Sanger Institute"

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  • SATSUMA : Highly sensitive whole-genome synteny alignments.

    Satsuma is a whole-genome synteny alignment program. It takes two genomes, computes...source code from here. Stable versions can also be downloaded from the Broad Institute's web site. An incomplete li...

    2927 days ago

  • Blobology

    Tools for making blobplots or Taxon-Annotated-GC-Coverage plots (TAGC plots) to visualise the contents of genome assembly data sets as a QC step Blaxter Lab, Institute of Evolutionary Biology, Univ...

    2896 days ago

  • AutoDock Vina: an open-source program for doing molecular docking.

    AutoDock Vina is an open-source program for doing molecular docking. It was des...bsp;Dr. Oleg Trott in the Molecular Graphics Lab at The Scripps Research Institute. It is especially effect...

    1435 days ago

  • Redundans

    Redundans pipeline assists an assembly of heterozygous genomes.Program takes as input assembled contigs,...genomes flexible toward many sequencing technologies (Illumina, 454 or Sanger) a...

    2816 days ago

  • Sybil

    The Sybil software package provides a primarily web-based...developed by the bioinformatics department at The Institute for Genomic Research (TIGR) and development continues at the J. Craig Venter Institute (JCVI) and the Institute for...

    2810 days ago

  • COSMIC

    The accurate description and annotation of structural variants can be complex.  This is due to the different...ure recommendations [http://www.hgvs.org/rec.html].  http://cancer.sanger.ac...

    2785 days ago

  • Spines

    Spines is a collection of software tools, developed and used by the Vertebrate Genome Biology Group at the Broad Institute. It provides basic data struc...

    2728 days ago

  • e-RGA: enhanced Reference Guided Assembly of Complex Genomes

    Next Generation Sequencing has totally changed genomics: we are able to produce huge amounts of data at an incredibly low cost compared to Sanger se...

    2707 days ago

  • Genome Assembly Tutorial

    If genomes were completely random sequences in a statistical sense, 'overlap-consensus-layout' method would have been enough to assemble large genomes from Sanger re...

    2706 days ago

  • Fastq format

    ...d quality score are each encoded with a single ASCII character for brevity. It was originally developed at the Wellcome Trust Sanger Institute to bundle a FASTA&n...

    2572 days ago