Results for "Long"

Tags

  • http://bioinfo.life.hust.edu.cn/lncRNASNP/ #long #noncodingRNA #SNP

    Tags: long, noncodingRNA, SNP

    3206 days ago

  • http://www.lncrnadb.org/ #long #noncodingRNA #DB

    Tags: long, noncodingRNA, DB

    3206 days ago

  • GraphMap - A highly sensitive and accurate mapper for long, error-prone reads

    GraphMap - A highly sensitive and accurate mapper for long, error-prone reads http://www.nature.com/ncomms/2016/160415/ncomms11307/full/ncomms11307.htmlFeatures    Mapping position agnostic to alignment parameters.    Consistently very high sensitivity and precision ...

    Tags: GraphMap, sensitive, accurate, mapper, long, error-prone, reads

    2508 days ago

  • miniasm: very fast OLC-based de novo assembler for noisy long reads

    Miniasm is a very fast OLC-based de novo assembler for noisy long reads. It takes all-vs-all read self-mappings (typically by minimap) as input and outputs an assembly graph in the GFA format. Different from mainstream assemblers, miniasm does not have a consensus step. I...

    Tags: Ultrafast, de novo, assembly, long, noisy, reads, consensus

    2335 days ago

  • MashMap: a fast and approximate software for mapping long reads (PacBio/ONT) or assembly to reference genome(s)

    MashMap is a fast and approximate software for mapping long reads (PacBio/ONT) or assembly to reference genome(s). It maps a query sequence against a reference region if and only if its estimated alignment identity is above a specified threshold. It does not compute the alignments explicitly, but...

    Tags: MashMap, fast, approximate, software, mapping, long, reads, PacBio, ONT, assembly, reference, genome(s)

    2319 days ago

  • LAMSA: fast split read alignment with long approximate matches

    LAMSA (Long Approximate Matches-based Split Aligner) is a novel split alignment approach with faster speed and good ability of handling SV events. It is well-suited to align long reads (over thousands of base-pairs). LAMSA takes takes the advantage of the rareness of SVs to implement a specifi...

    Tags: LAMSA, fast, split, read, alignment, long, approximate, matches

    2166 days ago

  • minialign: fast and accurate alignment tool for PacBio and Nanopore long reads

    Minialign is a little bit fast and moderately accurate nucleotide sequence alignment tool designed for PacBio and Nanopore long reads. It is built on three key algorithms, minimizer-based index of the minimap overlapper, array-based seed chaining, and SIMD-parallel Smith-Waterman-Gotoh extension.

    Tags: minialign, fast, accurate, alignment, tool, PacBio, Nanopore, long, reads

    2157 days ago

  • EAGLER: a scaffolding tool for long reads.

    EAGLER is a scaffolding tool for long reads. The scaffolder takes as input a draft genome created by any NGS assembler and a set of long reads. The long reads are used to extend the contigs present in the NGS draft and possibly join overlapping contigs. EAGLER supports both PacBio and Oxford Nano...

    Tags: EAGLER, scaffolding, tool, long, reads, genome, assembly

    2146 days ago

  • Cerulean: A hybrid assembly using high throughput short and long reads

    Cerulean extends contigs assembled using short read datasets like Illumina paired-end reads using long reads like PacBio RS long reads. Cerulean v0.1 has been implemented with bacterial genomes in mind. The method is fully described in Deshpande, V., Fung, E. D., Pham, S., & Bafna, V. (...

    Tags: Cerulean, hybrid, assembly, short, long, reads, pacbio, nanopore

    2145 days ago

  • HALC: High throughput algorithm for long read error correction

    HALC, a high throughput algorithm for long read error correction. HALC aligns the long reads to short read contigs from the same species with a relatively low identity requirement so that a long read region can be aligned to at least one contig region, including its true genome region’s repeats i...

    Tags: HALC, algorithm, long, read, error, correction, NGS, PacBio, Nanopore

    2141 days ago