Oncopro iMSI - Book Test at Low Cost

This examination helps evaluate the hazard of hereditary cancer. The examination encircles 98 genes targeting 25 hereditary cancer genes. The cancers encircled are Breast, Ovary, Uterine, Stomach, Endocrine Pancreas, Oesophagus, and other parts of body.

The Test

It is a next-era sequencing established examination for hereditary cancer exposure genes. The assay employs next-generation sequencing (NGS) to understand the coding sequences and intron/exon perimeters for the genes of the draw. The test has an elevated degree of analytical sensitivity and particularity. Confirmation capitalizing on industry-standard procedures resulted in an accuracy of >99.99%.

The Procedure

The sampling boxes will be shipped to the lab to investigate the DNA of precise genes to look for modifications in 98 genes linked with hereditary cancer hazards.

Benefits of the Test

Your outcomes may demonstrate you have modifications in certain areas of your DNA that boost your chance for specific kinds of hereditary cancer. Understanding that you have modifications in one or more of the

gene determination may assist you and your doctor make more knowledgeable healthcare determinations to stave off or see cancer situations at an early and potentially better treatable phase.

The designation of gene modifications in a family assists other blood families to specify whether or not they claim identical hereditary cancer chances. If testing examines that you retain genetic modifications, you should talk with your healthcare doctor

Risks of the Test

Some of the knowledge from the Test may be significant to your existing or fortune health. A genetic examination can indicate medically sensitive knowledge about you, containing the modifications that may induce chances of cancer for you or fellows of your family. The data may indicate that you may be at chance for specific cancer(s) or if you are a porter of cancer-associated modifications.

Boundaries of the Test

The procedure panel was scheduled to document SNV and Indels in coding areas. However, some structural deviations may not be seen. For a complete index of the current genes contained. The Test is aimed at detecting inherited genetic modifications on assigned genes known to be related to a raised chance for specific kinds of cancer.

Possible Test Outcomes

A positive outcome implies that a modification was specified in a particular gene that boosts your lifetime chance of expanding certain cancers. An optimistic outcome implies that you have inherited the modification from one or both of your parents. This outcome does not imply that you harbour cancer or that you will formulate cancer in your lifetime.

An unfavourable result implies that no modifications associated with a raised chance of evolving specific cancers were determined in the genes examined. This outcome does not wipe out your chance of evolving cancer.