Why do you need dna and genetic test?

DNA test in India is one of the genetic tests that is not only used as a dna detector as it goes beyond just tracking your genetic lineage. It is also efficient and productive in testing a genetic disorder that can affect you, and further, can pose a risk of passing on the same to your child. In order to find out chromosomal disorders during pregnancy, your doctor will advise you to go for a chromosome test or DNA test ancestry to rule out the possibility, address the risks if suffering from one and the measures or treatment plans to deal with its challenges. DNA ancestry test India is a widely common genetic test as it determines your past and digs your roots to find out more about your ancestors, their habitat, what kind of people they were and where they dwell all through their life, etc. 

What is the process of DNA test and genetic tests?

As there are different types of dna test available in today’s day and age, it is very important to understand how dna test is done and what is the significance of different genetic tests that exist in the medical sphere. You can opt for direct-to-consumer genetic and dna tests from Newmi or if you want to have your gene screening test done, then genetic ancestry test or Dna test online will offer wide scope of information like range of characteristics that your ancestry holds by studying the dna patterns and through them does mutation detection to identify the mutation in genes if any. The process of genetic test is very simple. A sample of your blood, hair, amniotic fluid or skin, and any other tissue in your body is assessed and studied by the lab. Post which, if the test results show a chance of genetic disorders, then further screening is recommended. 

Newmi offers specialised set of dna tests:

Cervical gland area marker: Ultrasound cga in pregnancy is advised to predict preterm birth. This sonographic marker identifies the relationship between absence of cga and preterm labor and research found that presence of cga in pregnancy is important to rule out the possibility of perinatal mortality which happens due to preterm labor.  

Whole Exome sequencing: Mitochondrial screening test checks for all clinically relevant 22000 genes plus 37 mitochondrial genes to check for any mitochondrial disorders. 

Factor V mutation detection: FVL or factor V mutation can give rise to preeclampsia and placental abruption, and is also a cause for miscarriages in pregnant women. Screening to find out mutation detection and is prescribed blood thinner treatment. 

Clinical Exome sequencing: This molecular diagnostic test checks for all clinically relevant 5900 genes including CNV and detects disease causing genetic mutation.

Genexpert ultra test: A molecular test that offers detection of MTB and rifampin resistance mutations.

There are other dna and genetic tests like carrier screening which studies gene panel of 2000 genes in couples to find out whether they are holding risk of passing inherited disorders to their children, or warfarin sensitivity testing to find out if you are sensitive to drug warfarin. Chromosome test like karkotyping analysis involves mode detailed analysis of your chromosomes like unique traits, your physical characteristics like eye color etc.