Test Catalog

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What we do

FRIGE is a pioneer and leader in providing world class diagnostic and counselling services, conducting cutting edge traslational research and training the next generation of scientists and clinicians. Our three-pronged approach ensures that the highest quality healthcare is provided to every patient that walks through our door.

Diagnostics

Genetics, endocrine and pathology diagnostic test provides information on why a patient is suffering from a given disease.

Genetic and pathology diagnostic test provides information on why a patient is suffering from a given disease. At FRIGE, we pride oursleves in providing a world class diagnostic service in genetics, endocrinology and pathology since 25 years. Our diagnostic test process are certified by ISO 9001:2015 and ERNDIM, the highest quality certification a diagnostic firm can obtain.

Our test suite is divided in 5 domains:

  • Cytogenetics
  • Molecular Genetics
  • Biochemical Genetics
  • Advanced Genomic Technologies
  • Pathology

With over 400 tests on offer, we have the largest suite of genetic and pathology tests in India that are available at an affordable price.

Genetic counselling

Genetic counselling is an informed discussion involving educating patients and their family members about cause, occurrence, diagnosis, recurrence and prevention of a genetic disorder in the family.

Genetic counselling is carried out by genetics’ experts who have an in-depth knowledge of various genetic tests that are available and have expertise in providing clinical support. Genetic counselling session involves the following:

  • Discussion of the genetic basis of patient’s clinical disorder and family’s clinical history
  • Availability of appropriate genetic tests for diagnosis
  • Treatment options, recurrence risk and family planning

Genetic counselling is recommended to patients facing one or more of the following situations:

  • Family history of a known genetic condition or birth defects
  • Consanguineous couples
  • General concern of would be parents about their child’s wellbeing
  • Bad obstetric history or multiple pregnancy loss
  • Death of a child with known/ unknown genetic condition
  • Prenatal ultrasound or marker screening suggestive of a genetic disease in the foetus
  • Child with dysmosphism, development delay or intellectual disability
  • Acquired genetic conditions (eg. cancer)

We provide both pre- and post-test counselling sessions. To know more or book an appointment, contact us.

Research

Our translation research ethos is to unravel basic biological processes, address biotechnological challenges and generating knowledge to improve human health in low-middle income countries.

We have a vibrant team of junior and senior research fellows, lab technicians and bioinformaticians with an expertise in molecular geneticis and computational biology. They work closely with the clinicians, genetic counsellors and diagnostics team to tackle some of the most challenging biotechnological barriers that are faced by low-middle income countries, such as India.

Our current research interests span following domains/ diseases:

  • Cost-effective and rapid diagnosis of lysosomal storage disorders (Funded by Gujarat State Biotech Mission)
  • Cost-effective and high-throughput NGS based microsatellite instability testing and Lynch syndrome detection (Funded by Gujarat State Biotech Mission and UK- Medical Research Council)
  • Aspirin or resistant starch based cancer chemoprevention in Lynch syndrome patients (Funded by Cancer Research UK)
  • Mutation spectrum of autism spectrum disorders in India (Funded by Gujarat State Biotech Mission)
  • ICMR’s Rare Disease Registry (Funded by Indian Council for Medical Research)

We are curious, ambitious and collaborative. We use state-of-the-art technologies, spanning:

  • Microarray
  • Next generation sequencing
  • Sanger sequencing
  • Cell culture
  • Data science

To date, we have published over 120 peer-reviewed publications and 2 books. We have also obtained patents on diagnostic tests that are used to diagnose I-cell disease and microsatellite instability in colorectal cancer. Click here to see past publications of Dr. Jayesh Sheth, Dr. Frenny Sheth and Dr. Harsh Sheth.

Our translational research is carried out in collaboration with national and international collaborators.

If you would like to know more or collaborate on one or more research themes, contact us.

Public engagement

Communication of latest scientific and technological developments to clinicians and public at large is at the heart of FRIGE's philosophy.

Each year, FRIGE organises a series of hands-on workshops, seminars and conferences in close collaboration with local, national and international agencies working on disseminating knowledge on rare genetic diseases.

Yearly highlight of our public engagement activity takes place on Rare Disease Day in February, where FRIGE organises a 1-day conference on diagnosis, screening, treatment and prevention of rare genetic disorders in Ahmedabad, India.

For more information on current and past public engagement events, click here.

Scientists, whether we like it or not, have a duty to shout about our research - and not just in the echo chambers of twitter or science conferences.

Peter Bickerton

Training, internships and dissertation

We have designed a set of unique educational and training opportunities in effort to bring together talented and intellectual students in order to bridge the gap between classrooms and real world.

The uniquely designed training offers exposure in the area of clinical genomics, sequencing and genetic counselling. This training is aimed at young professionals (with BSc / MSc / MRes / PhD / MBBS / MD degrees) in biotechnology or medicine who want to learn about clinical genomics in the era of high-throughput genomic technologies. The training is based on the teaching experinece established by FRIGE over past 25 years.

This laboratory-based training will provide a comprehensive overview of the theory and practical laboratory skills required for cytogenetics, FISH, microarray, Sanger sequencing, NGS, bioinformatics and genetic counselling. Training program includes following topics:

  • Cell culture and karyotyping
  • FISH and microarray preparation and analysis
  • Sanger sequencing workflow
  • Introduction to NGS
  • Bioinformatics and statistics
  • Genetic counselling

Training program is designed to inculcate self-directed outcome-based learning through a pedagogic teaching approach. Furthermore, formal lectures and one-to-one discussions are employed to simulate a real-world working environment.

Training duration is offered in 3 varieties:

  • 1 month- for a theoretical and practical overview of cytogenetics, molecular genetics and biochemical genetics. This is perfect for those who want to brush up on the latest genetic technologies.
  • 4 months- this hands-on-training is part of FRIGE-GSBTM Finishing School Training which covers all aspects of genetics, genomics and counselling. This is ideal for those who want to gain an in-depth theoretical and practical knowledge.
  • 6 months- this is ideally suited for an M.Sc. dissertation program whereby a dissertation project will provided and a short thesis will be written at the end of the training program.
  • Diploma certificate- this 6 months certificate course is suited for clinicians with MBBS or MD degree who would like to obtain an indepth knowledge and hand-on-training in all aspects of clinical and translational genetics.

To apply for the training program, fill out the online form here.

PhD studentships

There is no higher echelon in science than the doctorate of philosophy (Ph.D.)

We offer highly competitive and sort after Ph.D. studentships to those exceptional individuals who have been able to demonstrate their ability to solve complex problems with a creative approach.

Our Ph.D. studentship is recognised by Maharaja Sayajirao University, Baroda, India and is conducted jointly by both institutions.

We offer studentship in research projects encompassing one or more of the following:

  • Rare disease diagnostic techniques
  • Novel high-throughput sequencing based technology development
  • Disease epidemiology
  • High-throughput bioinformatics and computational biology

You can find our ongoing research here for more information.

Interviewing is a crucial part of our selection process. As we get to know you better, you will get the chance to know the institute better too. Successful applicants tend to:

  • Demonstrate intellectual curiosity
  • Communicate clearly and concisely
  • Analyse problems rigorously
  • Welcomes collaboration
  • Hold themselves and others to high standards
  • Have successfully cleared NEET/ GATE/ M.S. University entrance exam

If you think you have these qualities, apply here!