Results for "Genome"

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  • fragScaff: Genome Assembly with Contiguity Preserving Transposition

    Contiguity preserving transposition and sequencing (CPT-seq) is an entirely in vitro means of generating libraries comprised of 9216 indexed pools, each of which contains thousands of sparsely sequenced long fragments ranging from 5 kilobases to >1 megabase. This software, fragScaff, leverages...

    Tags: fragScaff, Genome, Assembly, Contiguity, Preserving, Transposition, Genome, Assembly

    2243 days ago

  • GAPPadder: A Sensitive Approach for Closing Gaps on Draft Genomes with Short Sequence Reads

    This software is provided ``as is” without warranty of any kind. In no event shall the author be held responsible for any damage resulting from the use of this software. The program package, including source codes, executables, and this documentation, is distributed free of charge. If you u...

    Tags: GAPPadder, Sensitive, Approach, Closing, Gaps, Draft, Genomes, Short, Sequence, Reads, Genome, Assembly

    2243 days ago

  • Hapsembler: An Assembler for Highly Polymorphic Genomes

    Hapsembler is a haplotype-specific genome assembly toolkit that is designed for genomes that are rich in SNPs and other types of polymorphism. Hapsembler can be used to assemble reads from a variety of platforms including Illumina and Roche/454. http://compbio.cs.toronto.edu/hapsembler/

    Tags: Hapsembler, Assembler, Polymorphic, Genomes, Assembly, Genome

    2235 days ago

  • Jvarkit : Java utilities for Bioinformatics

    Collection of Java tool kits for bioinformatics works: Jvarkit : Java utilities for Bioinformatics

    Tags: Bioinformatics, NGS, Java, toolkit, Genome, NGS, reads

    2218 days ago

  • GMcloser: closing gaps in assemblies accurately with a likelihood-based selection of contig or long-read alignments

    GMcloser uses likelihood-based classifiers calculated from the alignment statistics between scaffolds, contigs and paired-end reads to correctly assign contigs or long reads to gap regions of scaffolds, thereby achieving accurate and efficient gap closure. We demonstrate with sequencing data from...

    Tags: GMcloser, close, gaps, assemblies, accurately, likelihood-based, selection, contig, long-read, alignments, Genome, Assembly

    2215 days ago

  • SALSA: A tool to scaffold long read assemblies with Hi-C

    This code is used to scaffold your assemblies using Hi-C data. This version implements some improvements in the original SALSA algorithm. If you want to use the old version, it can be found in the old_salsa branch. To use the latest version, first run the following commands: cd SALSA m...

    Tags: SALSA, tool, scaffold, long, read, assemblies, Hi-C, Genome

    2211 days ago

  • CGView - Circular Genome Viewer

    CGView is a Java package for generating high quality, zoomable maps of circular genomes. Its primary purpose is to serve as a component of sequence annotation pipelines, as a means of generating visual output suitable for the web. Feature information and rendering options are supplied to the prog...

    Tags: CGView, Circular, Genome, Viewer, Bacteria

    2206 days ago

  • Genome in a Bottle http://jimb.stanford.edu/giab/ #GIAB #Genome

    Tags: GIAB, Genome

    2201 days ago

  • ASAR: Advanced metagenomic Sequence Analysis in R

    An interactive data analysis tool for selection, aggregation and visualization of metagenomic data is presented. Functional analysis with a SEED hierarchy and pathway diagram based on KEGG orthology based upon MG-RAST annotation results is available. To read the manual, please click the link&nbs...

    Tags: ASAR, Advanced, metagenomic, Sequence, Analysis, R, NGS, Genomics, Genome

    2187 days ago

  • http://qb.cshl.edu/assemblytics/ #Analysis #Genome #Mummer #Assembly #Assemblytics

    Tags: Analysis, Genome, Mummer, Assembly, Assemblytics

    2183 days ago