Increasingly, whole-genome sequencing of individuals is being done to help identify and treat medical conditions. Genome sequencing invariably identifies a number of variations, some common and some rare, that might be clinically relevant. For example, suppose a person had their genome sequenced to help determine their risk for cardiovascular disease and, just by chance, the sequence revealed that they carry one or more variants that predispose them to cancer or Alzheimer disease. Does the sequencing laboratory or physician have an obligation to report this finding, which was not the purpose of the sequencing and which the patient did not request? What about reporting variants for which no or limited information can be provided about their clinical significance? Does the answer to this question differ for sequencing done on children?

Q: List at least two ways in which computerized analysis oftranscriptomes aids genetic research.

A: Genetic research refers to the study of human deoxyribonucleic acid (DNA) to order to know the genes…

Q: Describe the mechanistic steps through which gene therapy might be used to cure a disease that is…

A: Gene therapy is a technique that uses genes to treat or prevent disease. Genes are the instructions…

Q: Genome Wide Associated Studies:   Question 7 options:   use SNP arrays to…

A: Approach to solving the question: a thorough way of answering. I hope this helps! Detailed…

Q: Being able to understand the relationship between DNA, mRNA, tRNA, ribosomes and proteins, is…

A: Sickle Cell Disease is an inherited blood disorder that affects the shape and function of red blood…

Q: Define deletion-insertion polymorphisms (DIPs)

A: Insertion is a mutation in which one or more nucleotide base pairs are added into a DNA sequence.…

Q: What is the ultimate goal of genetic engineers, describe (in detail) the methods used to achieve…

A: Genetic engineering is the science of manipulating the genetic material of an organism. The first…

Q: treat every genetically related health problem and to keep people alive at all cost. If this…

A: Each new genetic test conducted raises serious medical, public health, and social policy issues…

Q: Evaluate the complexity of the technical issues related to managing and utilizing genomic data as…

A: Genomic information relates to the composition and operation of the genome of an organism.  The…

Q: If companies like 23 and me should be allowed to sequence your DNA and give you the results instead…

A: 23andMe is a privately held personal genomics and biotechnology company based in Sunnyvale,…

Q: Mother = 2) Child ||| 16. 'Dad' 1 'Dad' 2 || 9) FAC 9) 'Dad' 3 Source:…

A: DNA fingerprinting or profiling refers to any DNA-based technique that identifies DNA from a…

Q: In 2003, the Human Genome Project was successfully completed, determining the exact sequence of the…

A: The Human Genome Project was an international scientific research project which efforts to determine…

Q: Sequencing the human genome, the development of microarray technology, and understanding of complex…

A: Proteomics is the large-scale study of proteins.Proteomics has enabled the identification of ever…

Q: Suppose a 10-year old patient has come to your office with a very rare disease. One so rare that…

A: The central dogma theory is an important concept in molecular biology that explains the flow of…

Q: you encounter an unknown disease  in humans and would like to understand the genetic mechanism for…

A: If a disease is genetic, this means that the gene or the DNA is not in a proper order. It is very…

Q: Genetic information from the Human Genome Project may be used to develop screening procedures which…

A: The Human Genome Project was an international, collaborative research project whose aim was to map…

Q: Which of the following describes forward genetics? Utilizing consensus regions within a genome to…

A: Genetics is the branch of biology that deals with the study of genes, their inheritance patterns,…

Genomic studies

Genomic studies (genomics) is the study of the whole genome of an organism. Using bioinformatics and high-performance computing, genomic researchers examined massive amounts of deoxyribonucleic acid (DNA)-sequence data to discover variations or mutations that affect drug response, health, or disease. Genomics is a much younger discipline than genetics, having only emerged in the last few decades as a result of technological advancements in DNA sequencing and computational biology.