A genome-wide approach to accurately detect point mutations. This can be both somatic mutations as well as germline mutations. The results will give you mutational load/frequency, spectrum and signatures.
Sequencing at the highest resolution
Sequence your DNA with unprecedented resolution
Our powerful Single Molecule Mutation Sequencing (SMM-seq (TM)) unlocks the ability to detect point mutations and structural variations in DNA, cells or tissue samples
Smm-SNV
Smm-SV
A genome-wide approach to detect structural variants with high accuracy. Unlike long-read WGS, the detection is not limited to the DNA input size and can detect structural variants that happen over a wider range. It detects the frequency of the variants and which specific ones occurred such as deletions, translocations, or inversions.
SMM-SNV Exome
Ultra-high def sequencing focused on the coding regions only.
SMM-SNV Targeted Panels
Ultra-high def sequencing focused on custom targeted panels
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