Results for "rapid"

Tags

  • TARDIS: Toolkit for automated and rapid discovery of structural variants

    tardis Toolkit for Automated and Rapid DIscovery of Structural variants Requirements zlib (http://www.zlib.net)mrfast (https://github.com/BilkentCompGen/mrfast)htslib (included as submodule; http://htslib.org/)Fetching tardis git clone https://github.com/BilkentCompGen/tardis.git --recursive ...

    Tags: TARDIS, Toolkit, automated, rapid, discovery, structural, variants

    2510 days ago

  • Manta: rapid detection of structural variants and indels for germline and cancer sequencing applications.

    Manta calls structural variants (SVs) and indels from mapped paired-end sequencing reads. It is optimized for analysis of germline variation in small sets of individuals and somatic variation in tumor/normal sample pairs. Manta discovers, assembles and scores large-scale SVs, medium-sized indels ...

    Tags: Manta, rapid, detection, structural, variants, indels, germline, cancer, sequencing, applications

    2157 days ago

  • HASLR: a tool for rapid genome assembly of long sequencing reads

    HASLR is a tool for rapid genome assembly of long sequencing reads. HASLR is a hybrid tool which means it requires long reads generated by Third Generation Sequencing technologies (such as PacBio or Oxford Nanopore) together with Next Generation Sequencing reads (such as Illumina) from the same s...

    Tags: HASLR, tool, rapid, genome, assembly, long, sequencing, reads

    1544 days ago

  • PyParanoid: a pipeline for rapid identification of homologous gene families in a set of genomes

    PyParanoid is a pipeline for rapid identification of homologous gene families in a set of genomes - a central task of any comparative genomics analysis. The "gold standard" for identifying homologs is to use reciprocal best hits (RBHs) which depends on performing a all-vs-all sequence comparison,...

    Tags: PyParanoid, pipeline, rapid, identification, homologous, gene, families, set, genomes

    1349 days ago

  • RITA: Rapid identification of high-confidence taxonomic assignments for metagenomic data

    RITA is a standalone software package and Web server for taxonomic assignment of metagenomic sequence reads. By combining homology predictions from BLAST or UBLAST with compositional classifications from a Naive Bayes classifier, RITA is able to achieve very high accuracy on short reads. Unlike o...

    Tags: Rapid, identification, high-confidence, taxonomic, assignments, metagenomic, data, RITA

    2339 days ago

  • alienness : Rapid Detection of Candidate Horizontal Gene Transfers across the Tree of Life

    Horizontal gene transfer (HGT) is the transmission of genes between organisms by other means than parental to offspring inheritance. While it is prevalent in prokaryotes, HGT is less frequent in eukaryotes and particularly in Metazoa. Here, we propose Alienness, a taxonomy-aware web application a...

    Tags: alienness, Rapid, Detection, Candidate, Horizontal, Gene, Transfers, Tree, Life

    2234 days ago

  • Snippy: Rapid haploid variant calling and core SNP phylogeny

    Snippy finds SNPs between a haploid reference genome and your NGS sequence reads. It will find both substitutions (snps) and insertions/deletions (indels). It will use as many CPUs as you can give it on a single computer (tested to 64 cores). It is designed with speed in mind, and produces a cons...

    Tags: Snippy, Rapid, haploid, variant, calling, core, SNP, phylogeny, bacteria

    2013 days ago

  • S-plot2: Rapid Visual and Statistical Analysis of Genomic Sequences

    S-plot2 creates an interactive, two-dimensional heatmap capturing the similarities and dissimilarities in nucleotide usage between genomic sequences (partial or complete). In S-plot2, whole eukaryotic chromosomes and smaller prokaryotic genomes can be efficiently compared. The tool includes funct...

    Tags: S-plot2, Rapid, Visual, Statistical, Analysis, Genomic, Sequences

    2029 days ago