Whole Genome re-Sequencing, (WGS)

Whole Genome re-Sequencing, (WGS)

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WGS compares the individual’s genomic sequence to a reference genome to identify genetic alterations specific to the individual – usually in the form of single nucleotide polymorphisms (SNPs), insertion/deletion (Indels), structural variation (SV) and copy number variation (CNV). 

WGS results are widely used in mutation detection, genetic map construction, functional gene mining, population evolution and artificial selection.