Results for "Exome Sequencing"

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  • CovCal: Coverage / Read Count Calculator

    Coverage / Read Count Calculator Calculate how much sequencing you need to hit a target depth of coverage (or vice versa). Instructions: set the read length/configuration and genome size, then s...

    2168 days ago

  • CNIDARIA: fast, reference-free phylogenomic clustering

    Motivation: Identification of biological specimens is a major requirement for a range of applications. Reference-free methods analyse unprocessed sequencing data without relying on prior...

    2882 days ago

  • Samtools Primer !!

    SAMtools: Primer / Tutorial by Ethan Cerami, Ph.D.keywords: samtools, next-gen, next-generation, sequencing, bowtie, sam, bam, primer, tu...

    2875 days ago

  • WgSim

    Reads simulator Wgsim is a small tool for simulating sequence reads fro...INDEL) polymorphisms, and simulate reads with uniform substitution sequencing errors. It does not generate INDEL sequencing errors, but this can be partl...

    2875 days ago

  • A5-miseq

    _A5-miseq_ is a pipeline for assembling DNA sequence data generated on the Illumina sequencing platform. This README will ta...

    2819 days ago

  • Kaiju

    Kaiju is a program for the taxonomic classification of metagenomic high-throughput sequencing reads. Each read is directly...

    2871 days ago

  • FQC Dashboard: Integrates FastQC results into a web-based, interactive, and extensible FASTQ quality control tool

    FQC is software that facilitates quality control of FASTQ files by carrying out a Q...metrics into an interactive dashboard designed to richly summarize individual sequencing runs. The dashboard groups sa...

    1274 days ago

  • MEGAN6

    Microbiome analysis using a single application MEGAN6 is a comprehensive toolbox f...you to work with hundreds of samples containing hundreds of millions of sequencing reads. Blast-like analysis ca...

    2843 days ago

  • Genome STRiP

    Genome STRiP (Genome STRucture In Populations) is...vering and genotyping structural variations using sequencing data. The methods are designe...heterogeneous data sets, including variations in sequencing depth, read lengths and mixtu...

    2800 days ago

  • TGNet

    Recent technological progress has greatly facilitated de novo genome sequencing. However, de novo a...

    2813 days ago