Results for "Genome"

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  • A5-miseq

    _A5-miseq_ is a pipeline for assembling DNA sequence data generated on the Illumina sequencing platform. This README will take you through the steps necessary for running _A5-miseq_. Point to note: There are many situations where A5-miseq is not the right tool for the job. In order to produce ...

    Tags: Bioinformatics, Analysis, NGS, A5-miseq, NGOPT Assembler, Genome

    2867 days ago

  • Genome Workbench 2.10.7

    Genome Workbench 2.10.7 is here! New features include added support for local custom BLAST databases and improvements to Tree View. For the full list of features, improvements and fixes, see the release notes:https://ncbi.nlm.nih.gov/tools/gbench/releasenotes New Features BLAST Tool: added s...

    Tags: Bioinformatics, Analysis, Visualization, Genome, Workbench, BLAST, Tree View.

    2915 days ago

  • 4DGenome

    Records in 4DGenome are compiled through comprehensive literature curation of experimentally-derived and computationally-predicted interactions. The current release contains 4,433,071 experimentally-derived and 3,605,176 computationally-predicted interactions in 5 organisms. Experimental data cov...

    Tags: Bioinformatics, 4DGenome, Database, Computational, Predicted, Interactions, Chromosome, Genome, NGS

    2912 days ago

  • What is genome? http://journals.plos.org/plosgenetics/article?id=10.1371/journal.pgen.1006181 #Genome #Definition #Genetics #Bioinformatics #Plos

    Tags: Genome, Definition, Genetics, Bioinformatics, Plos

    2891 days ago

  • Genome STRiP

    Genome STRiP (Genome STRucture In Populations) is a suite of tools for discovering and genotyping structural variations using sequencing data. The methods are designed to detect shared variation using data from multiple individuals.Genome STRiP looks both across and within a set of sequenced...

    Tags: Bioinformatics, Analysis, NGS, Genome STRiP, Genome, Variation

    2848 days ago

  • Genome and coverage https://rtsf.natsci.msu.edu/_rtsf/assets/File/depth%20and%20coverage.pdf #Coverage #Genome #Depth #Reads #NGS

    Tags: Coverage, Genome, Depth, Reads, NGS

    2772 days ago

  • VAGUE:Velvet Assembler Graphical Front End

    VAGUE is a vague acronym for "Velvet Assembler Graphical Front End", which means it is a GUI for the Velvet de novo assembler. The command line version of Velvet can be complicated for beginners to use, but VAGUE makes it clear and simple More at http://www.vicbioinformatics.com/software.va...

    Tags: Bioinformatics, Analysis, Assembly, Genome, VAGUE, Plot, View, Valvet

    2677 days ago

  • CrossMap

    CrossMap is a program for convenient conversion of genome coordinates (or annotation files) between different assemblies (such as Human hg18 (NCBI36) <> hg19 (GRCh37), Mouse mm9 (MGSCv37) <> mm10 (GRCm38)). It supports most commonly used file...

    Tags: Bioinformatics, Analysis, NGS, CrossMap, Genome, Coordinates

    2849 days ago

  • Long-read human genome sequencing and its applications https://www.nature.com/articles/s41576-020-0236-x #LongReads #Sequencing #Genome #Review

    Tags: LongReads, Sequencing, Genome, Review

    1476 days ago

  • OrganellarGenomeDRAW

    OrganellarGenomeDRAW is dedicated to convert genetic information stored in GenBank entries to graphical maps. The input text file has to be in GenBank flat file format, whereas the output format can be chosen among several formats. The application is especially optimized and adapted for the ...

    Tags: Bioinformatics, Analysis, NGS, OrganellarGenomeDRAW, Draw, Genome, OGDRAW

    2869 days ago