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Xenovea offers PCR-free Human WGS service @ 30X coverage for accurate variant detection using the Illumina NovaSeq platforms. 

Human Whole Genome Sequencing (WGS)

€679.00Price
  • Sample: ≥20 μl, ≥25 ng/μl High quality DNA

     

    Library preparation: NEXTFLEX Rapid XP DNA Seq Kit v2 with UDIs

     

    Inclusions (Sequencing, Bioinformatics, Raw data transfer): WGS analysis includes sample quality control, library preparation, final QC, sequencing and optinal full bioinformatic analysis (filtering, trimming, mapping, variant calling, annotation and reports); free data transfer of FastQ, Bam, Vcf files and Reports

     

    Sequencing metrics: Performed on Illumina NovaSeq with 2×150 bp paired-end run; Seq throughput: ≥ 30x genome coverage, Q30 ≥ 85%

     

    Quality control: Full quality assurance and guaranteed specifications

     

    Turnaround time: min. 2 – max. 4 weeks

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