Genetic Diagnostics

Enabling Precision Medicine

GeneComplete is the New Generation Genetics based diagnostic test for precision diagnosis.

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GeneComplete is a customizable Next Generation Sequencing (NGS) based Exome analysis. The cost effectiveness, advanced analytics, accuracy and expert counseling has made GeneComplete the popular choice among clinicians as a holistic genetic diagnostic solution.

Functional Areas

Diagnostics

Screening

Neurology Icon

Neurology

Muscular Dystrophy | Myopathy | Motor Neuron Disease | Neuropathy | Leukodystrophy | Epilepsy | Parkinson Disease | Dystonia

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Paediatrics Icon

Pediatrics

Inborn Errors of Metabolism | Musculoskeletal Disorders | Cranio-synostosis | Multisystem Syndromic Disorders| Disorders of Sexual Differentiation

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Oncology Icon

Oncology

Cancer screening

Oncology Icon

Oncology

Hereditary Cancer Syndromes | Gynecological Cancers | Gastro-Intestinal Cancers | Cancers of the Genito-urinary system | Cancers of the respiratory tract | Endocrinal Cancers

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Ophthalmology Icon

Opthalmology

Retinitis Pigmentosa | Glaucoma | Pediatric Cataracts | Corneal Dystrophies | Cone Rod Dystrophies | Norrie Disease | Retinoschisis | Keratoconus

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Endocrinology Icon

Endocrinology

Maturity-Onset Diabetes of the Young | Hyperinsulinemia and hypoglycemic syndromes | Hypogonadism and disorders of sexual differentiation | Pseudo hypo-aldosteronism

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Cardiology Icon

Cardiology

Dilated Cardiomyopathy | Hypertrophic Cardiomyopathy | Long QT Syndrome | Brugada Syndrome | Noonan Syndrome | Arrhythmias

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Gastroenterology Icon

Gastroenterology

Hemochromatosis | Wilsons Disease | Gilbert’s syndrome and Crigler Najjar syndrome | Prophyrias | Glycogen Storage Diseases | Familial GI Cancer syndromes | Congenital Hepatic Fibrosis | Hirschsprung disease

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Other Specialities Icon

Other Specialties

Albinism | Dyskeratosis | Epidemolysis Bullosa | Autism | Congenital Hearing Loss | Cystic Lung Disease | Bronchiectasis

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We use advanced Science & Technology

Next Generation Sequencing

Next Generation Sequencing is a technology to sequence the Genome (DNA) for determining the precise order of nucleotides (Adenine, Guanine, Cytosine, and Thymine) within a DNA molecule. It has greatly accelerated biological and medical research and discovery as the Knowledge of DNA sequences has become indispensable for medical diagnosis.

Whole Exome Analysis

The human genome consists of 3 billion nucleotides or “letters” of DNA. But only a small percentage — 1.5 percent — of those letters are actually translated into proteins, the functional players in the body. The “Exome” consists of all the genome’s exons, which are the coding portions of genes. Exome sequencing is a technique to sequence all the expressed genes in the genome.

Advanced Analytics

Transforming raw Genomics (DNA) data into accurate and actionable insights that are clinically relevant and useful to people’s life.

Sequencing

GeneComplete Advantage

Customization

GeneComplete offers a flexibility suite for analysis of gene(s) of interest, in addition to the well – established genes associated with the disease in question.

Disease-Gene Association

Panel of experts working on GeneComplete ensure an up – to – date and ready – to – use list to assist the clinician with the set of genes that need to be evaluated in various diseases.

High Sequencing Depth

Performed at a high sequencing depth for evaluation of various disease entities rendering a sensitivity and specificity of >99%, which is on par with other routine clinical diagnostics.

Advanced Analytics

Panel of experts working on GeneComplete ensure an up – to – date and ready – to – use list to assist the clinician with the set of genes that need to be evaluated in various diseases.

Intuitive Reports

The raw DNA data generated is interpreted by our team of experts and enriched with clinically relevant findings using authentic information from literature.

Pre / Post Test Clinical Support

Our medical experts verify the clinical relevance of the reports generated. Similarly, our R&D team also provides the most appropriate genetic testing method and also the clinical utility of various testing methods.

Additional Analysis

GeneComplete provides a unique advantage for rapid genetic analysis. For a patient previously evaluated with GeneComplete, any additional analysis of evolving clinical pattern or novel disease can be rapidly analyzed at nominal cost.

Functional Areas

GeneComplete is designed to understand and diagnose complex diseases in Neurology, Oncology, Cardiology, Pediatrics, Ophthalmology, Gastroenterology, Endocrinology, Metabolic and Carrier disorders.

GeneComplete for Doctors

Why should I prefer GeneComplete?

Doctor

GeneComplete greatly improves the speed and accuracy with which you can diagnose genetic disorders in children and adults. The discovery could lead to better care for people with rare diseases such as spinocerebellar ataxia, Cranio – synostosis, Retinoschisis, Arrhythmias and many other conditions in various disease areas. When GeneComplete is used with a complete patient evaluation and family medical history, the approach can help you identify disorders that may have gone undiagnosed for years. GeneComplete is very efficient and less expensive than many other genetic testing that has been more commonly used in routine medical diagnosis.

GeneComplete for Patients

Why should I go for GeneComplete?

Purpose

GeneComplete can be done to:

  1. Confirm a diagnosis that is already suspected based on medical history and examination.
  2. Determine the chance a healthy person is at risk or will develop a disease or condition in the future.
  3. Determine carrier status – a change in a specific gene or genes that increases the chance of having a child with a genetic disease.

Benefits

GeneComplete can be done to:

  1. Finding an increased risk of disease could lead you to choose preventive or therapeutic medical treatments that reduce the chance of developing the disease.
  2. Knowledge can empower you and your family members to make important life planning decisions, even if a cure is not available at this time.
  3. A specific diagnosis could qualify you to enroll in research studies, which may lead to new treatments.

Risks

  1. The physical risk of testing is usually minimal, typically not more than providing a blood sample.
  2. If your test involves any other type of sample, the physician performing the procedure or a designated representative, should explain the risks before you decide to get GeneComplete done.

Genetic Information

Your medical record and genetic test results are kept confidential. The results or the raw data is not shared or released to anyone without your written consent and authorization.

What We Do

What We Do Steps

Your DNA stores information that can help your doctor make accurate diagnosis enabling better quality of treatment for you.

To analyse your DNA, a small amount of your blood sample is collected by our phlebotomists and sent to our certified genetics lab where the DNA from your blood sample is extracted and purified for further processing.

The components of your DNA are now read using high end instruments known as Sequencers. Your DNA is read about a 100 times in short stretches thereby minimizing any chance of error.

Using advanced computing and bioinformatics tools your DNA is analysed and compared with DNA’s from 1000s of normal individuals. This enables our expert scientists to pinpoint to the location with likely abnormality in your DNA for a specific condition.

Finally your personalized genetic report is prepared by our Medical Scientists with suggested guidelines.

Your report is then ready to be used by your doctor to enable a more effective and precise management of your medical condition.

How it Works

How GeneComplete Works

  • Doctor-Patient Interaction

    You discuss the option of GeneComplete genetic test with your doctor.

  • Patient-InterpretOmics Discussion

    Talk to InterpretOmics Medical Geneticists (+91 8022535500) on GeneComplete test.

  • Order GeneComplete

    Please call to +91 8022535500 and request for sample collection from your home or hospital.

  • Whole Exome Sequencing

    We will sequence your DNA at our certified and accredited genetics lab.

  • Analysis and Interpretation

    Your DNA is analysed and interpreted for variants associated with your condition by our expert bioinformaticians, medical geneticists, and genetic counselors.

  • Reporting

    Your clinical diagnostics report is shared with your doctor.

  • Doctor-Patient Consultation

    You discuss your report with your doctor for next steps.

Order

Mail

Please talk to your doctor to know how you can get your GeneComplete done.

Phone

+91 8025212202

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