GENETIC TESTING &
MOLECULAR DIAGNOTICS
This area involves precise detection and analysis of genetic and molecular alterations that influence disease susceptibility, progression, and treatment responses. It is foundational to personalized and predictive medicine.
Key
Objectives
- Detection of inherited genetic mutations
- Genotyping for personalized therapy
- Understanding disease mechanisms at the molecular level
- SNP genotyping panels
- DNA/RNA extraction kits
- qPCR and digital PCR systems
- CRISPR-based molecular detection tools
- Bioinformatics platforms for result interpretation
Common Technologies
Typical Use Cases
- Carrier screening for genetic disorders (e.g., cystic fibrosis, BRCA mutations)
- Pharmacogenomic testing for drug response prediction
- Detection of genetic signatures in tumors
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“I greatly appreciate the communication on the very hard process, what we needed to do in terms of providing good samples, what to expect. Novalab laboratory provided tests what we needed in terms of laboratory certification that we can use with our customers.”
“I greatly appreciate the communication on the very hard process, what we needed to do in terms of providing good samples, what to expect. Novalab laboratory provided tests what we needed in terms of laboratory certification that we can use with our customers.”
“I greatly appreciate the communication on the very hard process, what we needed to do in terms of providing good samples, what to expect. Novalab laboratory provided tests what we needed in terms of laboratory certification that we can use with our customers.”