Mutation of the human genome ranges from single base-pair changes to whole-chromosome aneuploidy. Mutations are associated with a wide range of clinical problems, including cancer.
SNPs
Chromosome Abnormalities
Gene Fusions
Cancer Research Services
LC Sciences offers a range of services applicable to
clinical cancer research. Contact us to find out more.
The VariantPro system is an innovative multiplex PCR based targeted sequencing method that accomplishes target selection, library preparation and molecular tagging in a simple one-step workflow. [learn more…]
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. [learn more…]
The additional knowledge gained by studying the response to antigens at the epitope level will help us further understand anti-tumor immunity and may also help us to monitor cancer progress and cancer vaccine efficacy in the future. [learn more…]
Systems Biology has emerged as an effective approach to studying complex interactions within biological systems. By studying entire networks or pathways, we can better understand the underlying structure of cell signaling networks. [learn more…]
microRNAs are small noncoding RNA molecules that function broadly as negative regulators of gene expression to control a wide range of cellular processes. [learn more…]
Our comprehensive sequencing services make use of the latest in next-gen sequencing technologies. Illumina’s industry-leading RNA sequencing methods enable discovery [learn more…]