Pioneering Precision Health Through Genomic Insight
From Next-Generation Sequencing to Personalized Wellness—we empower research, clinical diagnostics, and R&D.
About Us: Crystallis health innovations
We are a leading diagnostic and research lab focused on leveraging the power of genomics to transform healthcare and scientific discovery. Our mission is to provide high-quality, actionable genomic data across clinical, research, and educational domains. We believe that precision health begins with precise data.
Our team comprises world-class geneticists, bioinformaticians, and healthcare professionals dedicated to setting new benchmarks in genomic testing and analysis.
Director's Message
"The next frontier in medicine is written in our DNA. By investing in robust R&D, developing Indian-origin specific panels, and fostering the next generation of genomic scientists through our training programs, we are not just analyzing data—we are building the future of personalized medicine."
— Dr. Rajeev Kumar Pandey, CEO & Founder
Comprehensive Genomic Services
Research Services: Advancing Discovery
Sanger Sequencing
- Microbial Identification (16S/18S /ITS/26S rRNA)
- Microsatellite Genotyping
- Cattle Genotyping
Next Generation Sequencing (NGS)
Comprehensive solutions across RNA, DNA, and Microbial samples.
DNA / RNA Sequencing:
Whole Crystallis/Exome, HLA Typing, Methylation, Amplicon Sequencing, ChIP Sequencing, mRNA/Total/Small/Single Cell RNA Sequencing.
Microbial Sequencing:
WGM (Shotgun Metagenomics), 16sRNA Sequencing, WGS (Microbial Monoculture).
Gene Expression (RT-PCR)
Services include gene expression, miRNA expression, SNP genotyping, copy number variation, and absolute quantification. Supports both TaqMan and SYBR Green chemistry.
Microarray Analysis
- Infinium Genotyping
- Crystallis Wide Association Studies (GWAS)
- Methylation Assays
- Agrigenomics Consortium Arrays
Supported Organisms & Samples:
Bacteria, Virus, Protists, Fungi, Plants, Animals, Humans. Samples from Blood, Tissue, Soil, Stool, Saliva, CSF, FFPE & more.
R & D: Our Innovation Pipeline
Cost-Effective NIPT Alternatives
Developing cost-effective, high-sensitivity alternatives to current NIPT methods, particularly suited for resource-constrained settings.
Early Cancer Detection (Liquid Biopsy)
- Circulating tumor DNA (ctDNA)
- Methylation profiling
- Cancer-specific mutation panels
Indian-Origin Specific NGS Panels
Creating Next-Generation Sequencing (NGS) panels tailored to the unique genetic diversity of the Indian subcontinent.
Proprietary Technology Platforms
- Proprietary bioinformatics pipelines for variant annotation, interpretation, and clinical reporting.
- Use of machine learning algorithms for pattern detection in large genomic datasets.
- Building cloud-based platforms for clinicians to access actionable insights from genomic data.
Comprehensive Genetic Support Services
Your health journey deserves more than just test results—it deserves guidance, clarity, and care at every step. Our Comprehensive Genetic Support Services bring together advanced diagnostics, expert report interpretation, and compassionate counseling, ensuring you never navigate your genetic information alone.
Personalized Lab Insights
Some tests require specialized partner laboratories—and we manage the entire process for you. From sample coordination to reviewing the final results, we ensure your report reflects accuracy, reliability, and personalized care.
“Your sample moves through advanced labs, but the trust stays with us.”
Sample Required: As per the test (blood, saliva, or tissue).
Precision Care Reporting
Every report carries responsibility. We interpret outsourced test results through our clinical lens and present them on our letterhead with clear, actionable insights.
You receive information that’s precise, understandable, and truly useful for making the right health decisions.
Sample Required: As per the test (blood, saliva, or tissue).
Genetic Counseling
Genetic information can feel overwhelming—but it doesn’t have to. Our certified genetic counselors help you understand your risks, review your results, and explore next steps with empathy and clarity.
It’s not just counseling—it’s a safe space to ask, learn, and choose what’s best for you and your family.
Sample Required: No sample required; appointment-based service.
Join Our Team
Be a part of a mission-driven organization at the forefront of genomic diagnostics. We are looking for passionate scientists, bioinformaticians, and healthcare experts.
View Openings (Coming Soon)