Human Whole Genome Sequencing

Sample type:

DNA

Turn-around

14 working days

Service details

Human whole genome sequencing (hWGS) allows researchers to map out the complete genetic makeup of individuals and analyze entire human genomes. This method facilitates the detection of various genomic variations, such as single-nucleotide polymorphisms (SNPs), insertions and deletions (InDels), structural variations (SVs), and copy number variations (CNVs), all within a single, cost-effective test.

Category

DNA Sequencing

Sub-category

Illumina NovaSeq 6000

* Contact us for quote

Please note that academic price involves subsidizing the production of data and KRISP members producing (max. two individuals) and/or analyzing data are normally co-authors to manuscripts. The commercial price include all costs and no-authorship or collaborationn is needed. Price can vary due to exchange rates, price last estimated at - 2024-01-01