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This document outlines the proposal by the National Human Genome Research Institute (NHGRI) to collect public feedback regarding genomics and its societal implications through surveys at the Smithsonian
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How to fill out Proposed Collection; Genomics and Society Public Surveys

01
Start by reviewing the purpose of the Genomics and Society Public Surveys to understand the context.
02
Gather all necessary documentation and guidelines related to the Proposed Collection.
03
Identify the target population for the surveys and establish the method of data collection.
04
Develop specific questions that will gather relevant genomic and societal insights.
05
Ensure that the surveys comply with ethical standards and obtain necessary approvals.
06
Pilot test the surveys with a small group to identify and correct any issues.
07
Finalize the survey design based on feedback from the pilot test.
08
Submit the Proposed Collection for review, including all relevant materials and documentation.

Who needs Proposed Collection; Genomics and Society Public Surveys?

01
Researchers in genomics and social science fields looking to gather public opinions.
02
Policy makers interested in understanding public attitudes towards genomics.
03
Healthcare professionals aiming to inform patients about genomic issues.
04
Advocacy groups seeking to represent public viewpoints on genomic technologies.
05
Educational institutions focusing on genomics as part of their curriculum.
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It refers to a set of public surveys designed to gather information and insights about public attitudes and perceptions regarding genomics and its impact on society.
Entities or individuals conducting research or assessment related to genomics and society may be required to file these surveys to comply with data collection protocols.
To fill out the surveys, respondents must follow the provided instructions carefully, ensuring all sections are completed with accurate and truthful information.
The purpose is to understand public perspective on genomics, facilitate informed decision-making, and contribute to policies that address the ethical, legal, and social implications of genomic research.
Respondents must report demographic information, opinions on genomics, personal experiences, and any relevant insights related to the broader societal implications of genomic advancements.
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