What is the purpose of Genomics and Cytogenetics testing?

Genomics testing analyzes your genetic makeup to identify mutations or variations that may cause diseases, while Cytogenetics focuses on detecting chromosomal abnormalities linked to genetic disorders or cancers.

What conditions can be diagnosed with Genomics and Cytogenetics testing?

These tests help diagnose inherited disorders, chromosomal abnormalities, cancers, and other genetic conditions. They are also useful in pre- and post-transplant immunology and prenatal screening.

How is Genomics and Cytogenetics testing performed?

Genomics testing typically involves blood, saliva, or tissue samples for DNA analysis, while Cytogenetics often uses blood or bone marrow samples to study chromosomes under a microscope.

Who should consider Genomics and Cytogenetics testing?

Individuals with a family history of genetic disorders, couples planning pregnancy, cancer patients, or those requiring organ transplants may benefit from these tests.

How do genetic testing services help in healthcare?

Genetic testing identifies specific mutations or variations in your DNA that can predict your risk for certain diseases, help in diagnosing conditions, and guide personalized treatment plans.

Why is chromosomal analysis important?

Chromosomal analysis detects structural or numerical abnormalities in chromosomes, which can be linked to genetic disorders, infertility, miscarriages, or certain cancers.

When is HLA typing required?

HLA typing is crucial for organ and bone marrow transplants to match donors and recipients, ensuring compatibility and reducing the risk of rejection.

How accurate are DNA analysis labs for genetic testing?

Reputed labs use advanced technologies like PCR and next-generation sequencing to ensure highly accurate results, minimizing errors in genetic evaluations.

What role does genetic testing play in diagnosing inherited disorders?

Genetic testing can confirm or rule out the presence of inherited disorders by identifying mutations passed down through generations, aiding in early intervention and management.

Can cytogenetic abnormalities be treated?

While cytogenetic abnormalities cannot be cured, early detection allows healthcare providers to manage associated conditions effectively and improve the patient's quality of life.

How long does it take to get the results for these Genomics and Cytogenetics tests?

The turnaround time varies depending on the test, ranging from a few days to a few weeks. Specific timelines can be confirmed during consultation.

Why choose Sprint Diagnostics for Genomics and Cytogenetics testing?

Sprint Diagnostics is the best genetic labs near you offering state-of-the-art technology, including LUMINEX for HLA typing and advanced molecular biology platforms, ensuring accurate and timely results.

Genetic Tests Diagnostic Center | Best Genetic Test Centers near me Hyderabad

Genetic and Cytogenetics

Genomics:

Genomics is the study of all of a person's genes (the genome), including interactions of those genes with each other and with the person's environment.

The genomics data helps in identifying variations that affect health, disease or drug response.

Techniques used here are:

1Next Generation Sequencing (NGS)
2Microarray etc.

Cytogenetics:

Cytogenetics involves testing of samples of tissue, blood or bone marrow to look for changes in chromosome including broken, missing, rearranged or extra chromosomes.

Techniques used here are karyotyping, banding, FISH etc

Common tests incude:

1Chromosomal analysis
2BCR/ABL gene
3Various AML mutations

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