What is NIPT? Noninvasive prenatal testing (NIPT), sometimes called a noninvasive prenatal screening test (NIPS), is a method of determining the risk that the fetus will be born with specific genetic abnormalities. It has been a little over two years since noninvasive prenatal testing (NIPT) was introduced as part of prenatal care to screen high-risk […]
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 […]
Genomics: Microarrays contain single-stranded oligonucleotides with sequences from the human genome to tile the area of interest specified to the surface. The relatively small scope of clinical utility and the slow early uptake can be attributed to the lack of clinical evidence supporting the use of medical genomics in multifactorial diseases. Indeed, as clinically important […]
What is the BRCA Gene Mutation? BRCA1 and BRCA2 are genes that suppress malignant tumours (cancer) in humans. When these genes change (become mutated) they do not suppress tumours as they should. BRCA1 and BRCA2 are tumour suppressor genes, which means that they keep cells from growing too rapidly. So people with BRCA1 and BRCA2 […]
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 DNA of alleged brothers or sisters to determine if they are full siblings, half-siblings or not related. This brother and sister DNA test can help prove or disprove paternity or maternity indirectly. DNA testing with siblings is the best option when the alleged […]
What is the Maternity DNA Test? A Maternity DNA test is a laboratory test in which the genetic material (DNA) of an alleged mother and child is analyzed to determine the likelihood that the tested woman is the biological mother of the child. Maternity testing is also sometimes used to confirm the biological links to […]
HLA Typing: Human leukocyte antigen (HLA) typing is a method to determine how closely a transplant recipient’s tissues match their potential donor’s tissues. Human leukocyte antigen (HLA) typing is used to match patients and donors for bone marrow or cord blood transplants. HLA are proteins, or markers, found on most cells in your body. HLA […]
The cost of a Sibling DNA test at DNA Labs India is ₹24,000. List sibling DNA test cost for sample type and relationship:- Test Name Test Cost Peace of Mind Sibling DNA Test Brother To Brother Cost: 24000.00 Peace of Mind Sibling DNA Test Brother To Sister Cost: 24000.00 Peace of Mind Sibling DNA Test […]
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.
