Results for "Reads"

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  • NextDenovo: string graph-based de novo assembler for TGS long reads

    NextDenovo is a string graph-based de novo assembler for TGS long reads. It uses a "correct-then-assemble" strategy similar to canu, but requires significantly less computing resources and storages. After assembly, the per-base error rate is about 97-98%, to further improve single base ...

    Tags: NextDenovo, NextOmics, string, graph-based, de novo, assembler, TGS, LongReads, assembly, long, reads

    1583 days ago

  • FastGT: an alignment-free method for calling common SNVs directly from raw sequencing reads

    FastGT is a program package for whole-genome genotyping of genome variants directly from raw sequencing reads. It is written in C and runs in Linux. FastGT uses a list of variant-specific k-mer pairs that are unique in human genome, counts the frequency of k-mers in sequencing data and predicts t...

    Tags: FastGT, alignment-free, method, calling, common, SNVs, directly, raw, sequencing, reads, alignment-free

    1560 days ago

  • HASLR: a tool for rapid genome assembly of long sequencing reads

    HASLR is a tool for rapid genome assembly of long sequencing reads. HASLR is a hybrid tool which means it requires long reads generated by Third Generation Sequencing technologies (such as PacBio or Oxford Nanopore) together with Next Generation Sequencing reads (such as Illumina) from the same s...

    Tags: HASLR, tool, rapid, genome, assembly, long, sequencing, reads

    1557 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

    1552 days ago

  • Free Genomics data !

    The specimens were collected by the Oxford Wytham Woods and Edinburgh Lohse lab teams. DNA extraction and sequencing was carried out by the Sanger Institute Scientific Operations teams. Assemblies were carried out by the Tree of Life team (Shane McCarthy) and colleagues in Pacific Biosciences (Jo...

    Tags: data, reads, free, tree, assembly

    1550 days ago

  • Deepbinner: a signal-level demultiplexer for Oxford Nanopore reads

    Deepbinner is a tool for demultiplexing barcoded Oxford Nanopore sequencing reads. It does this with a deep convolutional neural network classifier, using many of the architectural advances that have proven successful in image classification. Unlike other demultiplexers (e.g. Albacore and Porecho...

    Tags: Deepbinner, signal-level, demultiplexer, Oxford, Nanopore, reads, adaptor

    1547 days ago

  • Biological databases !

    Now a days there are a lots of genomics databases available around the world. This bookmark is created to provide all links in one place ... ftp://ftp.ncbi.nih.gov/genomes/ https://hgdownload.soe.ucsc.edu/downloads.html

    Tags: download, database, ncbi, ftp, genome, dna, reads, genome, assembly, files, ucsc

    1545 days ago

  • SLR-superscaffolder: A scaffold assemble pipeline for stLFR reads.

    This is a scaffold assembler designed for stLFR reads[1]. It uses the link-reads information from stLFR reads to assemble contigs to scaffolds. Here is an illustration of this pipeline:  

    Tags: SLR-superscaffolder, scaffold, assemble, pipeline, stLFR, reads

    1543 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

    1500 days ago

  • Filtlong: quality filtering tool for long reads

    Filtlong is a tool for filtering long reads by quality. It can take a set of long reads and produce a smaller, better subset. It uses both read length (longer is better) and read identity (higher is better) when choosing which reads pass the filter. Filtlong builds into a stand-alone executable:...

    Tags: Filtlong, quality, filtering, tool, long, reads

    1454 days ago