What is Karyotyping Karyotyping is a genetic test used to study an individual’s chromosomes. Every individual has 23 pairs of chromosomes or 46 chromosomes in our body, if there is one less or more chromosome in an individual, it creates genetic anomalies causing various genetic diseases. Karyotyping is used to diagnose genetic diseases, some birth […]
When is Karyotyping recommended? Karyotyping is recommended to check if there are any chromosomal abnormalities, whether it is structural or numerical. There are many situations in which a karyotype may be recommended by your physician. These might include: Infants or children who have medical conditions which suggest a chromosomal abnormality that has not yet been […]
Genetic tests for birth defects? If your doctor has recommended a Genetic test for birth defects for you or your child to diagnose any birth defects, there are various tests available to go for. Mostly all the birth defects are related to chromosomes which are due to structural or numerical changes, but there other tests […]
What is a Fluorescent in situ hybridization FISH DNA test? Fluorescence In-Situ Hybridization is a method used to identify specific parts of a chromosome. FISH can be used to detect small deletions and duplications that are not visible using microscope analysis like karyotyping. It can also be used to detect how many chromosomes of a certain type are […]
What is Whole Exome Sequencing? Whole Exome Sequencing (WES) is a cutting-edge genetic test designed to identify disease-causing mutations across thousands of genes. The exome, which represents the protein-coding regions of the genome (~1% of the human genome), contains around 85% of all disease-related mutations. By focusing on these coding regions, WES provides a highly […]
What is an Ancestry DNA Test? An Ancestry DNA test helps you discover your roots and genetic origins. It traces where your ancestors came from, the migration patterns of your family, and the percentage of DNA inherited from various regions worldwide. This test provides insights into your ethnic background, historical lineage, and familial migration over […]
What is a DNA Microarray Test? A DNA Microarray Test is a cutting-edge genomic technology designed to analyze thousands of genes simultaneously with high precision and speed. Unlike traditional PCR or qPCR, which examines a limited number of genes, microarray technology can detect multiple genetic variations, gene mutations, and expression patterns on a single platform. […]
Clinical Exome Sequencing (CES) is an advanced DNA test that analyzes all clinically relevant coding regions of the genome to identify genetic variations linked to health conditions. Using Next-Generation Sequencing (NGS) technology, CES provides accurate, comprehensive, and cost-effective insights into rare genetic disorders, complex diseases, and pharmacogenomic responses. What is Clinical Exome Sequencing? Clinical Exome […]
Liquid Biopsy DNA Test is a minimally invasive genetic test that helps detect molecular biomarkers and genetic variations without the need for traditional tissue biopsies. Using just a simple blood sample, this advanced test can provide critical information about cancer or other diseases, making it a safe, fast, and reliable alternative to surgery. What is […]
What is the cost of an Ophthalmological DNA test in India? The Cost of an Ophthalmological DNA test in India varies from 20 000 Rs depending on various gene locations and the type of methodology used for testing. You can book the DNA test from any city in India. Why do a DNA test? Genetic […]
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.
