Molecular Diagnostics
Molecular pathology solutions for clinical trials
Patients are waiting. That’s why Versiti scientists work closely to understand each specific study goal, customizing, optimizing, and implementing workflows. We provide SOPs and quality control processes needed for successful deployment and monitoring, ensuring every step brings us closer to delivering answers.
Supported Applications
Review the below sample of currently supported applications below. Contact Us to discuss your specific project needs to determine availability.
- T-cell receptor (TCR) sequencing
- Somatic mutation analysis
- RNA-Seq and miRNA-Seq
- Rare mutation detection
- Meticulously quantified molecular standards
- Sequence confirmation
- Fragment analysis
- Germ line and somatic genotyping
- Copy-number variation (DNA)
- Expression analysis of mRNA, miRNA, lncRNA
- Infectious disease assay development
- FFPE, FNA, LCM
- Whole blood, plasma, serum, PBMCs
- Stool, urine, nasal/pharyngeal, and buccal samples
- ELISA
- Immunogenicity
- Immunophenotyping
- Cell-cycle analysis
- Gene expression
- NK cell panel (quantification)
- Intra-sample NGS gene expression distribution
- Inter-sample differential gene expression (study group analysis)
- TCR repertoire analysis
High- Throughput Processing and Analysis
Versiti has the capacity to support testing and analysis at any scale. Our instrumentation and scalability, paired with highly skipped staff, can support projects ranging from small, pre-clinical research projects to large, high-throughput projects requiring tens of thousands of samples.
Our laboratories have been custom-built to accommodate good laboratory practices (GLP) and are equipped with instrumentation validated to multiple regulatory standards.
Bioproduction Quality Control (QC)
Establishing quality-control systems and reagents is a crucial step in the development of biological assays and agents for use in research and medicine. Our team has expert knowledge and experience in these systems, with professional backgrounds in both the pharmaceutical and biotechnology industries. QC services include:
- Residual DNA testing
- Synthetic assay standards
- Known-positive biological standards
- Standards for in-process checkpoints