![Centogene’s CentoMD® rare disease variant database will be integrated into Qiagen’s bioinformatics suite in a rare disease bioinformatics collaboration by the companies. [Source: alengo/Getty]](https://www.clinicalomics.com/wp-content/uploads/2019/01/1291-218x150.jpeg "Illumina Intros Genomic Analysis Workflow Software to Speed Diagnosis of Genetic Conditions")
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Molecular Dx
- RNA Sequencing
- Assay Development
- Cancer Testing
- Biodefense/Bioterrorism
- Cardiovascular Testing
- Cancer Transcriptome
- Liquid Biopsies
- Companion Diagnostics
- Cell-Based Assays
- Direct to Consumer Testing
- Comparative Genomic Hybridization
- Drugs of Abuse Testing
- DNA
- Genetic Disease Testing
- Infectious Disease Diagnostics
- Flow Cytometry
- Inherited Disease Diagnostics
- Laboratory Developed Tests (LDTs)
- Noninvasive Diagnostics
- Genotyping
- Point of Care Testing
- Immunoassay
- Prenatal/Postnatal Testing
- Immunochemistry
- Lab Equipment
- Metabolites
- Microarrays
- Microbiology
- Microfluidics
- Molecular Biology
- Molecular Diagnostics/In vitro Diagnostics
- PCR
- Pharmacogenomic Testing
- Pharmacokinetics
- RNA
- Reagents
- Sample Preparation
- Sequencing
- Single Cell Technology
- Single-Cell Genomics
- Toxicogenomics