Genomics for precision & decisions
We are your partners in making precise decisions for your patients. Enabling diagnostics to discovery & research for healtcare professionals via our global netwokr of CLIA & CAP certified labs. We are present in 15 countries across the globe known for our genomic data interpretations.
Specialities we serve
Our strengths
Our state -of-art interpretation platform for accurate & precise interpretation of genomics data for clinical reports built by geneticists & bioinformaticians to provide you latest & upto date reports.
Our team
50 member team of geneticists & Bioinformaticians to decode the genomic data.
Database
Access to latest global variant classification databases for comprehensive and high-quality reports for diagnosis of genetic conditions.
Algorithm
Our platform is built & capable of interpreting Whole-exome Sequencing (WXS) & Whole Genome Sequencing (WGS) data for advanced diagnostics.
Our panels
Over 3,000 genes have been chosen from curated gene reviews, variant databases (HGMD and ClinVar), the most recent research, and customer requests for our panels. Across all of our panels, we provide increased clinical value, increased diagnostic yield, aided differential diagnosis, and analytically confirmed up-to-date genes.
Comprehensive cardiology panel
The most efficient way to subtype inherited cardiovascular disorders is through genetic testing. It serves as the foundation for determining the best treatment option and making well-informed illness management decisions.
Comprehensive neurology panel
Nuerological disorders are complex to classify without accurate diagnostic tools. Genetics is the most efficient way to subtype neurological diseases, and provides the necessary information to make confident individualized treatment and management decisions.
Comprehensive nephrology panel
A range of single-gene illnesses, chromosomal abnormalities, and several multifactorial disorders are all genetic causes of kidney disease. Although a genetic cause may be hypothesised based on known family history or the incidence of other medical disorders at the same time, disease presentation in many cases is unanticipated.
Comprehensive Haematology panel
To confirm the diagnosis of some haematological malignancies and discover the best treatment for affected patients, an accurate genetic diagnosis is required. In addition to determining the underlying genetic abnormality and inheritance pattern, family member testing can be used to identify at-risk relatives.
How we work
We offer clinicians and their patients with comprehensive and high-quality reports for determination of hereditary conditions and various other conditions which have a strong genetic component. In doing so, we have follow quality assurance practices for outcomes that are focused on treatment and individualized care for patients.
Diagnosis
Decision of future course of action for any disease and conditions depends upon the accurate Diagnostic reports. We provide you that by using state-of-art platfrom powered by global databases for accurate variant classification and reporting.
Genetic Counselling
Our in house medical geneticist can help you & your patients understand the outcomes of the report as a counselling service.
Quality Assurance
Delivering quality reports is our mission to help you with precise information which will ease your decision making for future course of action.
powered by global databases for accurate
Contact Us
Contact Information
Fill up the form and our Team will get back to you within 24 hours.
(+91) 9004484303
sales@evolutiongenomics.com
601, Corporate Centre,Nirmal Lifestyle, LBS Marg,Mulund(West), Mumbai 400080
Contact Us
Contact Information
Fill up the form and our Team will get back to you within 24 hours.
(+91) 9004484303
sales@evolutiongenomics.com
601, Corporate Centre,Nirmal Lifestyle, LBS Marg,Mulund(West), Mumbai 400080
Contact Us
