Results for "RA"

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  • BreakSeq2

    Ultrafast and accurate nucleotide-resolution analysis of structural variants More at http://bioinform.github.io/breakseq2/ Download BreakSeq2 Latest version: https://github.com/bioinform/breakseq...

    3000 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 Hts-spec...

    2941 days ago

  • GA4GH Data Working Group

    ...e leading Genome Institutes and Centers with IT industry leaders to create global standards and tools for the secure, privacy respecting and interoperable sharing of Genomic data....

    2980 days ago

  • RNA-Seq De novo Assembly Using Trinity

    ...d robust de novo reconstruction of transcriptomes from RNA-seq data....ata into many individual de Bruijn graphs, each representing the tra...licing isoforms and to tease apart transcripts derived from paralogo...full read set among these disjoint graphs. Butterfly then proce...

    2978 days ago

  • Easyfig

    ...mjsull.github.io/Easyfig.  Easyfig is a Python application for creating linear comparison figures of multiple genomic loci with an easy-to-use graphical user interface (GUI)....

    2941 days ago

  • Awesome bioinformatics pipelines !

    A curated list of awesome pipeline toolkits ... https://github.com/pditommaso/awesome-pipeline

    2970 days ago

  • PhyloGrapher - Graph Visualization Tool

    PhyloGrapher is a program designed to visualize and study evolution...ologous genes or proteins (elements).PhyloGrapher is a drawing tool that generates custom graphs for a given...p; More at http://www.atgc.org/PhyloGrapher/PhyloGrapher_Welcome.html

    2963 days ago

  • PAired-eND Assembler for DNA sequences

    PANDASEQ is a program to align Illumina reads, optionally with PCR primers embedded in the sequence, and reconstruct an overlapping sequence.   More at https://github.com/neufeld/pandaseq

    2964 days ago

  • Sequence assembly with MIRA 4

    MIRA is a multi-pass DNA sequence data assem...whole genome and EST/RNASeq projects. MIRA assembles/maps reads gained b...r assemblies (a simple mapping). The MIRA acronym stands for Mimicking...n done efficiently - and especially accurately. That is, without me actu...

    2964 days ago

  • RACA: Reference-Assisted Chromosome Assembly

    Rreference-Assisted Chromosome Assembly (RACA), an algorithm to reliably order and orient sequence scaffolds generated by NGS and assemblers into longer chromosomal fragments using comparative genom...

    2964 days ago