Results for "illumina"

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  • Genome Assembly Tools and Software - PART2 !!

    ...potential with multi-library Illumina-based projects. GeneStitch 1...or assembling and scaffolding Illumina sequencing data of microbial...s in any draft assembly using Illumina paired end reads. IMAGE is be..., trace data (ABI, SCF, AB1), Illumina and Roche 454 flowgrams into...

    2684 days ago

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  • Illumina Ten X seq data released ! http://allseq.com/x-ten-test-data #Omics #Seq #1000$genomeData

    3565 days ago

  • http://www.forbes.com/sites/matthewherper/2014/08/21/illumina-partners-with-big-pharmato-create-new-genetic-tests-for-cancer/ #SeqStory

    3541 days ago

  • +3 more Wire posts

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  • Yannick Wurm Lab

    ...e for social phenotypes. We have been identifying genes and mechanisms involved in the evolution of insect societies using modern genomics tools (Illumina, RNAseq, RADseq...). For exam...

    3557 days ago

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Bio-Scripts

  • Downloading GATK !

    ...ls that process sequencing machine data, e.g. Illumina base calls, and detect sequen...ing level attributes, e.g. adapters CheckIlluminaDirectory (Picard)...Classify PF-Failing reads in a HiSeqX Illumina Basecalling directory into va...

    2074 days ago

  • Generate simulated polyploid genome !

    ...> toyheterozygous3percent.fasta #Cat both files cat toy.fasta toymutated3percent.fasta > toyheterozygous3percent.fasta #generated 50X of Illumina paired-end reads sim_reads...

    2052 days ago

  • +2 more Bio-Scripts

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  • Protocol for De novo Genome Assembly using Illumina Reads

    In this protocol, we address and describe the de novo assembly method for small to medium-sized genomes. What is de novo genome assembly?The method of taking a large number of short DNA sequences and placing them back together to create a reflection of the original chromosomes from which the DNA...

    Tags: Protocol, De novo, Genome, Assembly, Illumina, Reads

    1203 days ago

  • Illumina based assembly pipeline steps !

    Illumina Merge re-sequenced FastQ files (cat) Read QC (FastQC) Adapter trimming (fastp) Removal of host reads (Kraken 2; optional) Variant calling Read alignment (Bowtie 2) Sort and index alignments (SAMtools) Primer sequence removal (iVar; amplicon data only) Duplicate read marking (p...

    Tags: assembly, pipeline, genome, illumina

    876 days ago

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