Results for "sequencing"

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  • NanoPack: visualizing and processing long-read sequencing data

    The NanoPack tools are written in Python3 and released under the GNU GPL3.0 License. The source code can be found at https://github.com/wdecoster/nanopack, together with links to separate scripts and their documentation. The scripts are compatible with Linux, Mac OS and the MS Windows 10 subsyste...

    Tags: NanoPack, visualizing, processing, long-read, sequencing, data, ngs

    1970 days ago

  • EXCAVATOR: detecting copy number variants from whole-exome sequencing data

    EXCAVATOR, for the detection of copy number variants (CNVs) from whole-exome sequencing data. EXCAVATOR combines a three-step normalization procedure with a novel heterogeneous hidden Markov model algorithm and a calling method that classifies genomic regions into five copy number states. We vali...

    Tags: EXCAVATOR, detect, copy, number, variants, whole-exome, sequencing, data

    1961 days ago

  • NGS Platforms launched by BGI’s MGI Tech

    MGI Tech Co., Ltd. (MGI), a subsidiary of BGI Group, is committed to enabling effective and affordable healthcare solutions for all. Based on its proprietary technology, MGI produces sequencing devices, equipment, consumables and reagents to support life science research, medicine and healthcare....

    Tags: MGI, china, genomics, BGI Group, announced, pricing, ultra, high-throughput, sequencer, MGISEQ-T7, sequencing, cost, gigabyte

    1955 days ago

  • Katuali is a flexible consensus pipeline implemented in Snakemake to basecall, assemble, and polish Oxford Nanopore Technologies' sequencing data

    Run a pipeline processing fast5s to a consensus in a single command. Recommended fixed "standard" and "fast" pipelines. Interchange basecaller, assembler, and consensus components of the pipelines simply by changing the target filepath. Seemless distribution of tasks over local or distribute...

    Tags: Katuali, flexible, consensus, pipeline, Snakemake, basecall, assemble, polish, Oxford, Nanopore, Technology, sequencing, data

    1943 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

    1872 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

    1778 days ago

  • jackalope: A swift, versatile phylogenomic and high-throughput sequencing simulator

    jackalope simply and efficiently simulates (i) variants from reference genomes and (ii) reads from both Illumina and Pacific Biosciences (PacBio) platforms. It can either read reference genomes from FASTA files or simulate new ones. Genomic variants can be simulated using summary statistics, phyl...

    Tags: jackalope, swift, versatile, phylogenomic, high-throughput, sequencing, simulator, ngs

    1758 days ago

  • Prof. Dr. med. Andreas Ramming

    In many autoimmune diseases, a misdirected immune response leads to chronic inflammation and subsequently to fibrotic and degenerative tissue remodeling. Therapeutic options are available for inflammatory joint diseases, but only about 40% of patients respond to these existing therapies on a perm...

    Tags: Immunology, sequencing, single cell, mathematics, fibrosis, arthritis, mouse model

    1746 days ago

  • mosdepth: fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing

    mosdepth can output: per-base depth about 2x as fast samtools depth--about 25 minutes of CPU time for a 30X genome.mean per-window depth given a window size--as would be used for CNV calling.the mean per-region given a BED file of regions.a distribution of proportion of bases covered at or above...

    Tags: mosdepth, fast, BAM, CRAM, depth, calculation, WGS, exome, target, sequencing

    1644 days ago

  • https://www.cartana.se/ #Brain #Single #cell #sequencing

    Tags: Brain, Single, cell, sequencing

    1569 days ago