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Explanation: Thats all i got i hope it helps if not im sorry im having a bad morning
Answer:
Explanation:
Transcription takes place in nucleus in the presence of the enzyme RNA polymerase.
During transcription, the code present in DNA gets transcribed into the code in mRNA. (messenger RNA)
RNA even though is a single stranded shows base pairing.
The pre-mRNA gets created from the DNA.
DNA has two strands, one of these strands acts as coding and another non coding strand.
The DNA shows base pairing with AGTC. [A-Adenine, G- Guanine, T-Thymine and C- Cytosine]
Whereas mRNA base pairing with AGUC. [ U- Uracil ]
Here in mRNA, instead of thymine, uracil gets paired.
According to base pairing of coding strand/sense strand of DNA, complementary bases pairs in 5'---->3' direction in mRNA.
The mRNA created looks exactly like the non-coding strand/sense strand of DNA except instead of thymine, uracil gets replaced.
The pre-RNA undergoes splicing, capping and tailing to form mature mRNA.
The correct answer s act late in the disease.
Disease:
- When tumor DNA is studied from cancer patients at various stages, the mutation will be comparable in all of them. Tumor DNA is frequently identified in the blood stream.
- Disease is any adverse variation from an organism's normal structural or functional condition that is typically accompanied by a set of symptoms and is distinct from physical injury in origin.
- illnesses. An abnormal state of an organism that interferes with its normal bodily functioning, frequently causes pain and weakness, and is typically accompanied by symptoms and indicators.
- Disorders produced by organisms, infectious diseases are those caused by microorganisms such bacteria, viruses, fungi, or parasites. Numerous species live inside of our bodies. They are generally advantageous or even secure. But in specific circumstances, some bacteria have the capacity to cause disease.
Learn more about disease here brainly.com/question/19813896
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Answer:
By changing a gene's instructions for making a protein, a mutation can cause the protein to malfunction or to be missing entirely. When a mutation alters a protein that plays a critical role in the body, it can disrupt normal development or cause a medical condition.