In addition, we can assist in:
Identification of genetic variants
Identification on somatic mutations in tumors
Identification on putative disease causing variants from exomes/genomes
Identification and quantification of mutations in common tumor genes
Providing: data management for whole genome association, targeted, or linkage studies; tracking genotypic and phenotypic data in databases, with capabilities for managing phenotypes, family-structures, genotypes, samples, plates, SNP/STR, maps, output to analysis packages, and more. We manage all types of samples and associated data in customizable multi-level inventories that can be developed into laboratory workflows.