I'm conducting a survey for a research project about genome sequencing, if you have time to answer some or all of these questions I would really appreciate it. Feel free to add any additional information or questions you feel relevant. This is an open forum for all thoughts and ideas regarding this topic.
As some or all of you may know in 2003 the human genome project was completed. It took 10 years and cost 3 billion dollars. Today a collection of companies offer personal DNA sequencing from $800-1000 US dollars. Scientists and research companies are creating large open-source public DNA data pools online for anyone to access. Volunteers are donating their DNA data to be studied by genomic scientists and researches around the world.
1. Do you agree with public / open-source DNA databases, yes or no? Why?
2. What do you think are the biggest risks associated with an individual publishing their DNA sequence online?
3. How do you feel about genetic discrimination?
4. Do you agree with GINA - Genetic Information Nondiscrimination Act?
5. Currently GINA protects genetic discrimination regarding some types of health insurance, it does not restrict life insurance and long-term disability insurance companies from using an individual's genetic sequence to determine coverage. How do you feel about this?
6. Personal DNA sequence tests are rapidly becoming cheaper and more accessible, what kind of predictions do you imagine in the future when all people will know and understand their DNA sequence? Examples: - Advantage - healthcare will become more personalized, doctors will examine your DNA sequence and formulate personalized vitamins, regiments, and medications specific to each patient's needs. Disadvantage - DNA sequence accessibility could lead to a dystopian future where their DNA sequence could cause lose of employment opportunities, insurance plans, etc.
If you're interested please answer as many of the questions as you like. Thank you!
As some or all of you may know in 2003 the human genome project was completed. It took 10 years and cost 3 billion dollars. Today a collection of companies offer personal DNA sequencing from $800-1000 US dollars. Scientists and research companies are creating large open-source public DNA data pools online for anyone to access. Volunteers are donating their DNA data to be studied by genomic scientists and researches around the world.
1. Do you agree with public / open-source DNA databases, yes or no? Why?
2. What do you think are the biggest risks associated with an individual publishing their DNA sequence online?
3. How do you feel about genetic discrimination?
4. Do you agree with GINA - Genetic Information Nondiscrimination Act?
5. Currently GINA protects genetic discrimination regarding some types of health insurance, it does not restrict life insurance and long-term disability insurance companies from using an individual's genetic sequence to determine coverage. How do you feel about this?
6. Personal DNA sequence tests are rapidly becoming cheaper and more accessible, what kind of predictions do you imagine in the future when all people will know and understand their DNA sequence? Examples: - Advantage - healthcare will become more personalized, doctors will examine your DNA sequence and formulate personalized vitamins, regiments, and medications specific to each patient's needs. Disadvantage - DNA sequence accessibility could lead to a dystopian future where their DNA sequence could cause lose of employment opportunities, insurance plans, etc.
If you're interested please answer as many of the questions as you like. Thank you!