Whole genome sequencing (WGS) is a powerful technique that enables researchers to analyze an organism's complete DNA sequence. By comparing this sequence to a reference genome, researchers can detect genetic variations or use the data to create a new genome assembly. WGS can also be used to identify and classify microbial or viral species present in a sample. WGS libraries can be generated from as little as 1 ng DNA.

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For additional information, please contact:

 Liat Linde, tel 073-3785452 or 077-8875168

Rappaport building 073-3785221

Emerson building 077-8871387