Sequencing of a child's genomic DNA reveals that the child is a heterozygote for a new mutation. This mutation appears in all of the cells tested from a variety of tissues (including skin, blood, and hair). The mutation is not found in either the mother or the father. Most likely, this is a new ____ mutation that occurred in O germ line; one of the parents O germ line; the child O somatic; the child Osomatic; one of the parents O germ line; both of the parents

Most likely, this is a new somatic mutation that is to occur in a child which appears in all of the cells tested from a variety of tissues.

So, the correct option is C.

Using whole genome sequencing, you can examine and contrast the germline DNA of your child with the DNA of cancer or tumor cells. We may learn more about the specific diagnosis and course of treatment for your child from these, which can vary. Deciphering the genetic material found in an organism or virus is done by scientists using a process called genomic sequencing. According to scientists, the spread of a virus, how it is changing, and how those changes may affect public health can all be tracked by comparing sequences from specimens.

In genetic syndromes, two types of tests are used: molecular and cytogenetic. In general, methods such as restriction enzyme digestion, DNA hybridization, and/or direct sequencing are used to detect single-base pair mutations.

Learn to know more about Genomic DNA on

https://brainly.com/question/26266533

#SPJ4