MutationForecaster
The Shannon pipeline software is used for high throughput interpretation of genomic variation. Other programs in this suite include the CytoVa database, and Veridical for validating splicing mutations with RNASeq evidence.
High accuracy prediction of non-coding mutations, such as those affecting mRNA splicing. Proven approach based on information theory.
ADCI
The Automated Dicentric Chromosome Identifier and Dose Estimator analyzes human metaphase images to determine levels of absorbed ionizing radiation from blood samples. See our wiki.
Single Copy (sc) technology: precise, sensitive, and informative genomic hybridization tools for genetic disease management
Molecular cytogenomic products include:
- Fluorescent in-situ hybridization scFISH probes from our catalog or custom synthesized,
- Microarray designs for comparative genomic hybridization, and
- Targeted solution capture arrays for hybridization enrichment in deep sequencing. (DISCONTINUED)
The FISH probes offer the highest resolution available on the market. The genomic microarrays use sc technology to increase reproducibility and reduce cost per sample. The solution capture arrays offer the highest genomic coverage available on the market for next generation sequencing.
