Results for "accurate"

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  • P_RNA_scaffolder: a fast and accurate genome scaffolder using paired-end RNA-sequencing reads

    P_RNA_scaffolder is a novel scaffolding tool using Pair-end RNA-seq to scaffold genome fragments. The method is suitable for most genomes. The program could utilize Illumina Paired-end RNA-sequencing reads from target speciesies. Our method provides another practical alternative to existing mate-...

    Tags: P_RNA_scaffolder, fast, accurate, genome, scaffolder, paired-end, RNA, sequencing, reads, scaffold

    2061 days ago

  • Flye: Fast and accurate de novo assembler for single molecule sequencing reads

    Flye is a de novo assembler for single molecule sequencing reads, such as those produced by PacBio and Oxford Nanopore Technologies. It is designed for a wide range of datasets, from small bacterial projects to large mammalian-scale assemblies. The package represents a complete pipeline: it takes...

    Tags: Flye, Fast, accurate, de novo, assembler, single, molecule, sequencing, reads, ngs, assembly

    1854 days ago

  • Flye: Fast and accurate de novo assembler for single molecule sequencing reads

    Flye is a de novo assembler for single molecule sequencing reads, such as those produced by PacBio and Oxford Nanopore Technologies. It is designed for a wide range of datasets, from small bacterial projects to large mammalian-scale assemblies. The package represents a complete pipeline: it takes...

    Tags: Fast, accurate, de novo, assembler, single, molecule, sequencing, reads

    1759 days ago

  • MSAProbs - Parallel and accurate multiple sequence alignment

    MSAProbs is a well-established state-of-the-art multiple sequence alignment algorithm for protein sequences. The design of MSAProbs is based on a combination of pair hidden Markov models and partition functions to calculate posterior probabilities. Assessed using the popular benchmarks: BAli...

    Tags: MSAProbs, Parallel, accurate, multiple, sequence, alignment

    1756 days ago

  • Rcorrector: efficient and accurate error correction for Illumina RNA-seq reads

    Rcorrector has an accuracy higher than or comparable to existing methods, including the only other method (SEECER) designed for RNA-seq reads, and is more time and memory efficient. With a 5 GB memory footprint for 100 million reads, it can be run on virtually any desktop or server. The software ...

    Tags: Rcorrector, efficient, accurate, error, correction, Illumina, RNA-seq, reads

    1546 days ago

  • CLARK: Fast, accurate and versatile sequence classification system

    CLARK, a method based on a supervised sequence classification using discriminative k-mers. Considering two distinct specific classification problems (see the article for details), namely (1) the taxonomic classification of metagenomic reads to known bacterial genomes, and (2) the assignment ...

    Tags: CLARK, Fast, accurate, versatile, sequence, classification, system, bacteria

    1535 days ago

  • HiCanu: accurate assembly of segmental duplications, satellites, and allelic variants from high-fidelity long reads

    HiCanu, a significant modification of the Canu assembler designed to leverage the full potential of HiFi reads via homopolymer compression, overlap-based error correction, and aggressive false overlap filtering.  More at https://www.biorxiv.org/content/10.1101/2020.03.14.992248v3

    Tags: HiCanu, accurate, assembly, segmental, duplications, satellites, allelic, variants, high-fidelity, long, reads

    1494 days ago

  • Liftoff: an accurate tool that maps annotations in GFF or GTF between assemblies

     Liftoff, an accurate tool that maps annotations in GFF or GTF between assemblies of the same, or closely-related species. Unlike current coordinate lift-over tools which require a pre-generated “chain” file as input, Liftoff is a standalone tool that takes two genome assemblies ...

    Tags: Liftoff, accurate, tool, maps, annotations, GFF, GTF, assemblies

    1399 days ago

  • DADA2: Fast and accurate sample inference from amplicon data with single-nucleotide resolution

    The DADA2 tutorial goes through a typical workflow for paired end Illumina Miseq data: raw amplicon sequencing data is processed into the table of exact amplicon sequence variants (ASVs) present in each sample. The DADA2 Workflow on Big Data goes through workflow op...

    Tags: DADA2, Fast, accurate, sample, inference, amplicon, data, single-nucleotide, resolution

    1266 days ago

  • Liftoff: An accurate GFF3/GTF lift over pipeline

    Liftoff is a tool that accurately maps annotations in GFF or GTF between assemblies of the same, or closely-related species. Unlike current coordinate lift-over tools which require a pre-generated “chain” file as input, Liftoff is a standalone tool that takes two genome assemblies and...

    Tags: Liftoff, accurate, GFF3, GTF, lift, pipeline

    1226 days ago