About Us

Helix GenoCare is a Genetic Testing Service Provider, emphasizing comprehensive pre- and post-test genetic counseling to ensure accurate test selection and meaningful results. A dedicated team of specialists performs a secondary review of every report, aligning outcomes with the patient's clinical history for maximum accuracy. Helix also serves as a knowledge-sharing platform for clinicians, helping them address genetic queries and enhancing awareness about test utility. The company focuses strongly on screening for common yet impactful conditions where early detection makes a difference—such as prenatal screening for hemoglobinopathies and trisomies, newborn screening, and screening for breast and cervical cancer. Through its SCoPE initiative (Screening, Counseling, and Preventing by Early Diagnosis of Hemoglobinopathies), Helix targets newborns, students, premarital, and prenatal populations. The introduction of Gazelle, an automated point-of-care tool for Beta Thalassemia and Sickle Cell Disease, enhances accessibility. Helix also has a special focus on Molecular Allergology, the 4th Generation In-vitro test for Allergy Diagnostics. Providing CRD based test reports enables a better endo-typing of patients, resulting in personalized care.



Our Mission

At Helix GenoCare, our mission is to provide high-quality healthcare services to our patients. We strive to make our patients feel comfortable and cared for during every visit.



Our Services

We offer a wide range of services to meet the healthcare needs of our patients. From routine check-ups to specialized treatments, we've got you covered.



Our Team

Our team consists of highly skilled and experienced healthcare professionals who are dedicated to providing the best possible care to our patients.



Careers

At Helix Genocare, we are building a global team of amazing people who want to change the way companies hire. If you are curious and ready to grow your career with us, we would like to meet you.

Tests and Services



QFPCR (for Prenatal samples)


Trio Whole Exome Sequencing


Spinal Muscular Atrophy (SMA1 & SMA2)- MLPA


DMD (Duchenne muscular dystrophy)- MLPA Based 79 exons


MS-MLPA for Beckwith-Wiedemann syndrome (BWS)


MS-MLPA for Angelmann Syndrome


MS-MLPA for Prader-Willi Syndrome (PWS)


Sanger Sequencing for single & multiple variants


Non-Invasive Prenatal Screening (NIPS)


Whole Exome Sequencing


Newborn Screening Tests


Autism Spectrum Panels


Chromosomal Microarray LD (315k)


Chromosomal Microarray HD (750k)


Single gene testing by NGS


Mitochondrial Genome Sequencing


Neuro Genetic Panels


Whole Genome Sequencing


Prenatal Screening Tests


Allergy Specific Tests


Pathology Routine Tests


Endocrinology Genetic Panels


Gastroenterology Genetic Panels


Karyotyping/Couple Karyotyping


Cardiac Genetic Panels


Thalassemia Mutation testing


Hereditary Cancer Panels


BRCA1/2 Gene Sequencing


Basic 7 Newborn Conditions


TMS/GCMS


Y Chromosome Microdeletion (YCMD)


Fragile X by TP-PCR

Why is genetic testing so important?

Genetic testing holds significant importance in India due to the country's diverse genetic landscape and high prevalence of genetic disorders. Here are key reasons why genetic testing is crucial in India:

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High Prevalence of Genetic Disorders:

India has a high incidence of genetic disorders such as thalassemia, sickle cell anemia, cystic fibrosis, and hemophilia, among others. Genetic testing helps in early identification of these conditions, enabling timely intervention.

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Carrier Screening:

Many genetic disorders are inherited in an autosomal recessive manner, meaning that carriers are typically asymptomatic. In regions with a high prevalence of certain genetic conditions, carrier screening can identify individuals at risk of passing these disorders to their offspring.

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Personalized Medicine:

Genetic testing allows for personalized treatment plans based on an individual's genetic makeup. This is particularly relevant for conditions like cancer, where targeted therapies can be more effective.

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Prevention of Genetic Disorders:

Prenatal and preconception genetic testing can help in preventing the birth of children with severe genetic conditions. This is especially important in communities where consanguineous marriages are common.

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Public Health Planning:

Genetic testing data can inform public health policies, helping to allocate resources effectively and develop targeted screening programs in regions with high prevalence of specific genetic disorders.

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Family Planning:

Couples can make informed decisions about family planning based on genetic testing results, reducing the risk of transmitting genetic disorders to their children.

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Awareness and Education:

Genetic testing can raise awareness about genetic disorders and encourage people to seek early testing and counseling, reducing the stigma associated with genetic diseases.

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Research and Development:

Genetic testing contributes to research in genomics and personalized medicine, helping India to develop its capabilities in biotechnology and healthcare.

Better yet, see us in person!

We love our patients, so feel free to visit during normal business hours.

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