Results for "BroadInstitute"

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  • Next Generation Sequencing (NGS) Tutorials

    ...ysis of next-generation sequencing data. http://www.ncbi.nlm.nih.gov/pubmed/23657089 GATK: a Toolkit for Genome Analysis http://www.broadinstitute.org/gatk/ Metagenomics:http:...

    3479 days ago

  • Integrative Genomics Viewer (IGV) tutorial

    ...that employs a reference genome, including how reads from a dataset are mapped, gene annotations, and predicted genetic variants. http://www.broadinstitute.org/igv/...

    3576 days ago

  • Pilon

    ...substitution events Gap filling Identification of local misassemblies, including optional opening of new gaps More at https://github.com/broadinstitute/pilon/wiki...

    3000 days ago

  • Spines

    ...diverged sequences; and SLAP, a context-sensitive local aligner for diverged sequences with large gaps. Access Spines here. http://www.broadinstitute.org/science/programs/genome-b...

    2999 days ago

  • RNA-Seq De novo Assembly Using Trinity

    Trinity, developed at the Broad Institute and the Hebrew University of Jerusalem, represents a novel method for the efficient and robust de novo reconstruction of transcrip...

    2956 days ago

  • Picard

    Picard is a set of command line tools for manipulating high-throughput sequencing (HTS) data and formats such as SAM/BAM/CRAM and VCF. These file formats are defined in the...

    2919 days ago

  • DISCOVAR

    ...DISCOVAR de novo can generate de novo assemblies for both large and small genomes. It currently does not call variants. More at https://www.broadinstitute.org/software/discovar/blog/?p...

    2930 days ago

  • MEDEA: Comparative Genomic Visualization with Adobe Flash

    ...power of the human visual system to detect trends and spot outliers is necessary in such large and complex data sets. More at http://www.broadinstitute.org/annotation/medea/

    2922 days ago

  • SATSUMA : Highly sensitive whole-genome synteny alignments.

    Satsuma is a whole-genome synteny alignment program. It takes two genomes, computes alignments, and then keeps only the parts that are orthologous, i.e. following the conse...

    2905 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 structures for effic...

    2706 days ago