Genomic Solutions 

Whole Genome Sequencing (WGS)

Whole genome sequencing provides a comprehensive analysis of entire genomes. This method can detect single nucleotide variants, insertions or deletions, copy number changes, and large structural variants in the genome analyzed. 

Whole Exome Sequencing (WES)

Whole exome sequencing involves sequencing of the protein coding regions of the genome making this method a cost-effective alternative to whole genome sequencing. This approach allows identification of genetic variations underlying many cancers and genetic diseases.

Amplicon Sequencing

Amplicon sequencing or ultra-deep sequencing of PCR products allows to analyze genetic variations in specific genomic regions. It is useful for the discovery of rare somatic mutations in complex samples. This approach is a time- and cost-effective alternative to whole genome sequencing.

Target Gene Sequencing

Target gene sequencing is an effective approach for analyzing selected gene(s) of interest by next generation sequencing. This approach provides higher coverage of the target region compared to WGS and  allows better identification of rare variants.