Single nucleotide polymorphisms (SNPs) are the most frequent type of genetic mutation in the human genome. An SNP located within the coding sequence of a gene may lead to susceptibility to human diseases, such as cancer.

SNP Detection Solutions

LC Sciences offers both targeted and whole genome sequencing services for SNP detection.
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Ordering Instructions

VariantPro™ Targeted Sequencing

The VariantPro™ system is an innovative multiplex PCR based targeted sequencing method that accomplishes target selection, library prep…

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Exome Sequencing

Exome sequencing is an efficient strategy to selectively sequence the coding regions of the genome as a less expensive but still effective alternative to whole genome sequencing…

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Targeted Sequencing – Capture Oligos

By targeting specific genomic regions, one can take better advantage of next-gen sequencing capability; essentially, more coverage is achieved by focusing reads on your area of interest…

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CANCER
RESEARCH
NEUROLOGICAL DISORDERS
CARDIOVASCULAR DISEASE
METABOLIC DISEASES