About Us
AR Genomics – One-Stop Solution for Genetic Services
Argenomics is a name synonymous with exceptional quality and service. Since its inception 3 years ago, Argenomics has continuously evolved with the passage of time and has now grown into a 'State-of-the-Art' Medical Genetic Laboratory. Modern laboratory services, along with extensive research and development taking place in this facility, make it, one of the best in the whole country. Argenomics is now equipped with the latest Next Generation Sequencing (NGS) system and the ION-S5 XL from Thermo Scientific U.S, which in fact, is the first such installation in the whole of South Asia and the Middle East.
We provide all Genetic Services under one roof. This includes Genetic counselling, Cytogenetic Services, Molecular Genetic Services and PGD/PGS. In a short span of time, Argenomics has developed a leading centre for reproductive genetic services in India. Patients are referred for genetic counselling as well as testing from all over the country, as well as from UAE, UK, USA, and Maldives.
One of the major reasons for the recurring pregnancy losses and IVF failures is a disorder occurring in the endometrium which mainly concerns abnormal gene expressions. Now using the procedure Endometrial Receptor Gene Assay (ERGA), it is possible to...
This is the prenatal genetic testing of foetal chromosomal aneuploidies from Mother’s Blood. We have the credit of being the first centre in the Indian subcontinent to develop in-house Non-Invasive Prenatal Testing (NIPT) which is 99.9% sensiti...
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Medical Genetics Block, Craft Hospital & Research Centre,
Chandapura , Kodungallur , Thrissur -680664Kerala,India
Tel:0480 2800267
Ph : +91 7736260302, +91 9544184222
E-mail : info@argenomics.org
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cytogenetics
Cytogenetics refers to the study of chromosome content in a cell. Argenomics has a fully equipped Cytogenetics lab with automated Karyotyping and FISH software. A complete Karyotype including structural chromosomal abnormalities and micro-deletions can be obtained using this facility. FISH is only performed on selected chromosomes. Cytogenetic studies can be done on a variety of samples like Peripheral blood, Amniotic fluid, CVS, and products of conception.
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Hereditary Disease
Targeted Mutation Screening is a diagnostic tool completed through blood test that identifies the mutated gene or genes causing a genetic disease in your family. The identification of a gene mutations allows for further steps to be taken to prevent the passing on of the condition to future generations and may aid in the improvement of treatment of an affected individual. In most cases, after identifying the cause of genetic disease the couples can go with a Pre-Implantation Genetic Diagnosis (PGD) for Single Gene Disorders, a genetic test...
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REPRODUCTIVE GENETICS
Preconception genetic testing Pre-Implantation Genetic Screening (PGS) involves a process of screening of embryos in the course of In Vitro Fertilization (IVF). This helps to identify abnormalities in the chromosomes occurring due to aneuploidy. The main reason for recurrent IVF failures and in turn pregnancy losses is the higher risk of chromosomal errors that happ...