Results for "variant calling"

Users

  • Ravindra Raut

    About me: ...using next-generation sequencing technologies like shotgun sequencing, linked reads, and long-read sequencing for whole-genome resequencing, variant calling, and transcriptome assembly,...Skills: Variant Calling

    1102 days ago

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Files

  • Bioinformatics approach to Boar Taint

    ...onable to many consumers. Detected functional variant(s) underlying boar taint comp...y using Bowtie2. Alignment file then used for calling SNPs and InDels inside previo...SSC5,13, and 7 with the aid of FreeBayes , a variant caller tool. A final list of...

    3751 days ago

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Wire posts

  • WGS/WES Mapping to Variant Calls - Version 1.0! http://www.htslib.org/workflow/ #Omics #NGS #WGS #SNP

    3507 days ago

  • VirVarSeq: a low frequency Virus Variant detection pipeline http://bioinformatics.oxfordjournals.org/content/early/2014/08/31/bioinformatics.btu587.abstract #Pipeline #Variant #VirVarSeq

    3482 days ago

  • +11 more Wire posts

News

  • Scalpel

    ...or simple sequence repeats that are a regular source of error in indel calling. When Scalpel assembles an ex...ffected siblings, a pattern that persisted even after excluding common variants.

    3508 days ago

  • Roche has acquired Bina Technologies !!!

    ...y based in California. The biotech’s first product was the Bina Box, a platform for secondary genomic analysis, sequence alignment, and variant calling, but since 2012, it has devel...

    3376 days ago

  • +11 more News

Opportunity posts

Bio-Scripts

  • Downloading GATK !

    ...eads in a HiSeqX Illumina Basecalling directory into various catego...sequencing data. CollectVariantCallingMetrics (Picard)...---------------------- Short Variant Discovery:...Tools that perform variant calling and genotyping for short vari...

    2037 days ago

  • Plot VCF with R !

    library(vcfR) # Input the files. vcf

    2022 days ago

  • +4 more Bio-Scripts

Tags

  • NGS Online Training

    ArrayGen Technologies announces to provide online NGS training through out the globe. Now analyze your own NGS datasets from anywhere.For more information contact us at training@arraygen.com Please visit our site at www.arraygen.com

    Tags: Bioinformatics, NGS Data Analysis, Genomics, Exome sequencing, variant calling

    3470 days ago

  • Webinar on Fast and Accurate DNA Variant Calling on 26 Apr 2017

    Continuing our DNA-Seq webinar series, we'll present Strand NGS v3.0 best-practices: a workflow that identifies highly accurate variants from raw reads. Our best practices workflow is twice as fast as its GATK counterpart, and results in precision/recall rates of up to 99%/98% on whole exome...

    Tags: webinar, strand ngs, variant calling, dna-seq, bwa-gatk

    2533 days ago

  • +2 more Tags

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