Results for "Genomes"

Tags

  • ALLHiC: Phasing and scaffolding polyploid genomes based on Hi-C data

    The major problem of scaffolding polyploid genome is that Hi-C signals are frequently detected between allelic haplotypes and any existing stat of art Hi-C scaffolding program links the allelic haplotypes together. To solve the problem, we developed a new Hi-C scaffolding pipeline, called ALLHIC,...

    Tags: ALLHiC, Phasing, scaffolding, polyploid, genomes, Hi-C, data, assembly

    1962 days ago

  • TRITEX sequence assembly pipeline for Triticeae genomes

    The pipeline is open-source and hosted in a public Bitbucket repository. TRITEX has been run on highly inbred genotypes of barley (Hordeum vulgare), tetraploid wheat (Triticum turgidum) and hexaploid wheat (T. aestivum) with reasonable results: super-scaffold N50 values in the range o...

    Tags: TRITEX, sequence, assembly, pipeline, Triticeae, genomes

    1719 days ago

  • Gepard: allows the calculation of dotplots even for large sequences like chromosomes or bacterial genomes

    Gepard (German: "cheetah", Backronym for "GEnome PAir - Rapid Dotter") allows the calculation of dotplots even for large sequences like chromosomes or bacterial genomes. Reference: Krumsiek J, Arnold R, Rattei T. Gepard: A rapid and sensitive tool for creating dotplots on genome scale. Bioinforma...

    Tags: Gepard, calculation, dotplots, sequences, chromosomes, bacterial, genomes

    1713 days ago

  • MFannot : a program for the annotation of mitochondrial and plastid genomes

    MFannot is a program for the annotation of mitochondrial and plastid genomes MFannot is a program for the annotation of mitochondrial and plastid genomes. It is a PERL wrapper around a set of diverse, external independent tools. It makes intense use of RNA/intron detection tools including ...

    Tags: MFannot, program, annotation, mitochondrial, plastid, genomes

    1713 days ago

  • HaploTypo: a variant-calling pipeline for phased genomes

    An increasing number of phased (i.e. with resolved haplotypes) reference genomes are available. However, most genetic variant calling tools do not explicitly account for haplotype structure. Here, we present HaploTypo, a pipeline tailored to resolve haplotypes in genetic variation analyses. Haplo...

    Tags: HaploTypo, variant-calling, pipeline, phased, genomes

    1598 days ago

  • Kevler: Reference-free variant discovery in large eukaryotic genomes

    Welcome to kevlar, software for predicting de novo genetic variants without mapping reads to a reference genome! kevlar's k-mer abundance based method calls single nucleotide variants (SNVs), multinucleotide variants (MNVs), insertion/deletion variants (indels), and structural...

    Tags: Reference-free, variant, discovery, large, eukaryotic, genomes, snp, ngs

    1559 days ago

  • mutatrix: a population genome simulator which generates simulated genomes.

    genome simulation across a population with zeta-distributed allele frequency, snps, insertions, deletions, and multi-nucleotide polymorphisms More at https://github.com/ekg/mutatrix ./mutatrix -S sample -P test/ -p 2 -n 10 reference.fasta

    Tags: mutatrix, population, genome, simulator, generates, simulated, genomes, ngs, test

    1559 days ago

  • Chromonomer: a tool set for repairing and enhancing assembled genomes through integration of genetic maps and conserved synteny

    Chromonomer is a program designed to integrate a genome assembly with a genetic map. Chromonomer tries very hard to identify and remove markers that are out of order in the genetic map, when considered against their local assembly order; and to identify scaffolds that have been incorrectly assemb...

    Tags: Chromonomer, tool, repairing, enhancing, assembled, genomes, integration, genetic, maps, conserved, synteny

    1539 days ago

  • RefKA: A fast and efficient long-read genome assembly approach for large and complex genomes

    RefKA, a reference-based approach for long read genome assembly. This approach relies on breaking up a closely related reference genome into bins, aligning k-mers unique to each bin with PacBio reads, and then assembling each bin in parallel followed by a final bin-stitching step.  

    Tags: RefKA, fast, efficient, long-read, genome, assembly, approach, large, complex, genomes

    1465 days ago

  • CAT/BAT: tool for taxonomic classification of contigs and metagenome-assembled genomes (MAGs)

    Contig Annotation Tool (CAT) and Bin Annotation Tool (BAT) are pipelines for the taxonomic classification of long DNA sequences and metagenome assembled genomes (MAGs/bins) of both known and (highly) unknown microorganisms, as generated by contemporary metagenomics studies. The core algorithm of ...

    Tags: CAT/BAT, tool, taxonomic, classification, contigs, metagenome, assembled, genomes, MAGs

    1447 days ago