DNA Extraction (if applicable)
Initial DNA QC
Library Preparation
Sequencing
Alignment and variant calling
Data Delivery
Library Preparation Kit: Illumina TruSeq DNA PCR-Free Library Prep Kit
Sequencing Platform: Illumina NovaSeq 6000
Read Type: Paired-end
Read Length: 150 bp
Sequencing Depth: Total mean coverage of ~30X
(alternative coverage options available upon request)
Initial DNA QC Report (.pdf)
Raw data file (.fastq) (available upon request)
Alignment file (.cram) (BAM file available upon request)
Variant file (.vcf)
Sequencing QC Metrics Report (.pdf)
2-3 weeks for a batch of up to 96 samples
For detailed information about the sample requirements for our Whole Genome Sequencing service, please consult our sample requirements page.