This nonfiction book is both more and less than I expected it to be. The authors cover the use of genomic testing (DNA seqyencing) for medical screening. But they also talk of a future when everyone will have a genomic analysis in their medical records. In addition, they talk about prenatal genetic testing for many more diseases or predispositins for disease. They dicuss the ethics of all the screening and the need for informed consent.
This book should focus on the meaning of informed consent, the history of informed consent, and the current Federal Requirements for informed consent for research. They seem to assume a working knowledge of genetics and yet give general background on many aspects of the testing. i found it to be too technical to be focused on the general population. But I did not see anything to indicate that it was geared towards more experienced readers.
I have a good background in genetics and DNA testing as well as the requirements for informed consent in the USA. However, the sections on future testing and the ethics of creating large databases without proper consent to be interesting and unexpected in this book.
I believe this is an important addition to the topic for the general population, but perhaps too much for a lay person to plough through. Still I rated it at a 4 because it kept me engaged throughout and added ideas I had not thought about before.