Quantum Testing

The quantum testing is based on the use of spectral analysis of eddy magnet fields which every biological organism has. These fields are commonly known as ‘bio-fields’. It is the bio-field which carries information inside the cell as well as among different cells or groups of cells in the living organism as a whole.

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Quantum DNA Analysis

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About genes

Genes are specific segments of DNA code which if decoded correctly by the proteins in our body, give specific and significant instructions about its right function.

Up till now scientists have calculated that there are about 22,000 genes contained in our genome. Although genes are of paramount importance, they represent but a small percentage of the whole DNA in the genome. Each gene has a concrete location on one of our 23 chromosomes and is inherited from generation to generation as a unit.

We have got two copies of each chromosome and hence two copies for each gene. We inherit one copy from each of our parents and we in turn give one of our two copies to each of our children.

What is a genetic disease?

Although genetic factors play a role in almost all health characteristics, there are a few conditions which are almost entirely caused by genetic transformations. Those are called genetic malformations or congenital disorders. Since genes are passed on from parent to child, all changes in the gene are also passed on. The changes in the DNA can crop up spontaneously, too, by occurring for the first time in a child of healthy parents. This is being recorded as a new mutation, where the word “mutation” means change. Sometimes this change can result in errors in the instructions for protein and this leads to the production of protein which does not work correctly or fails to form altogether. When one kind of protein is missing or not working properly, this can cause a genetic disorder.

When do congenital diseases occur?

Genetic disorders are passed on either by dominant or recessive way. When the disorder is dominant, the disease can occur when there are errors in one the two copies of the gene. This means that if the parent has got a change in their DNA, there is a 50% chance to pass it on to each child.

When the disorder is recessive, there must be errors in both copies of the gene to show a malfunction. That means that both parents must carry at least one copy of the specific change in the gene in order to give birth to an affected child. In this case the risk of having a genetic disorder in the child is 25%. The parents who have only one mutated genetic copy usually do not show any symptoms of the disorder and may even be unaware that they are carrying a mutated gene. Researchers reckon that each of us carries 6-10 recessive mutations.