What is Exome Sequencing? Exome sequencing, which sequences the protein-coding region of the genome, has been rapidly applied to variant discovery in research settings, and recent increases in the accuracy have enabled the development of clinical exome sequencing (CES) for mutation identification in patients with suspected genetic diseases. Exome sequencing, also known as whole-exome sequencing […]
Whole Exome Sequencing (WES) is revolutionizing how genetic disorders are diagnosed and understood. If you or your child has a complex or unexplained medical condition, WES could provide the answers you’ve been looking for. In this blog, you’ll learn: Quick Overview of WES Feature Details Test Name Whole Exome Sequencing (WES) Technology Next-Generation Sequencing (NGS) […]
What is the BRCA Gene Mutation? BRCA1 and BRCA2 are tumor suppressor genes that help control cell growth. When these genes are mutated, they cannot prevent abnormal cell growth, leading to an increased risk of cancer. Who Should Consider BRCA1/2 Genetic Testing? You may need BRCA testing if you have: 👉 Speak to a genetic […]
What Is HIV? HIV ( human immunodeficiency virus ) is a virus that attacks cells that help the body fight infection, making a person more vulnerable to other infections and diseases. It is spread by contact with certain bodily fluids of a person with HIV (human immunodeficiency virus), most commonly during unprotected sex, or through […]
What is an allergy? An allergy is an exaggerated reaction by the immune system in response to exposure to certain foreign substances. The response is exaggerated because these foreign substances usually are seen as harmless by the immune system in nonallergic individuals and do not cause a reaction in them. In allergic individuals, the body […]
What is a Sibling DNA Test? A sibling DNA test analyzes the genetic profiles of two or more individuals to determine if they are full siblings, half-siblings, or unrelated. 👉 This test is often used when the alleged father or mother is unavailable for direct paternity or maternity testing. Why Take a Sibling DNA Test? […]
A Maternity DNA Test in India is a highly accurate genetic test used to determine whether a woman is the biological mother of a child. While paternity testing is more common, maternity DNA testing plays a vital role in adoption cases, IVF confirmations, and legal disputes. In this guide, we’ll explain: What is a Maternity […]
Human Leukocyte Antigen (HLA) typing is a vital test used to match patients with compatible donors for organ, bone marrow, or stem cell transplants. At DNA Labs India, we offer accurate and reliable HLA Typing tests using advanced molecular techniques to ensure the best outcomes for transplant procedures. In India, the cost of an HLA […]
What is a Sibling DNA Test? A Sibling DNA Test determines whether two individuals share one or both biological parents. This genetic analysis helps confirm full-sibling, half-sibling, or unrelated relationships—especially when the alleged father is unavailable for paternity testing. Sibling DNA tests are widely used for personal peace of mind, property disputes, legal evidence, and missing child […]
Karyotyping: Karyotyping is a laboratory technique used to culture dividing cells and prepare their chromosomes for analysis. A karyotype refers to the arranged visual profile of chromosomes, organized by size, shape, and banding pattern, using either manual or computer-assisted methods. Karyotype analysis involves growing viable cells in culture and arresting them at the metaphase stage […]
DNA Labs India is renowned for utilizing cutting-edge technology to ensure the highest levels of accuracy and precision in their testing results. Their advanced laboratories and equipment guarantee that your DNA analysis is conducted with the utmost rigor.
