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Data_science_notes[1]
Data_science_notes[1]
Data scientists must have an in-depth knowledge and respect for data ethics for
several reasons. First, they work with large amounts of sensitive and personal
data which must be handled responsibly to avoid privacy breaches that
compromise individuals. Second, data scientists often create models which impact
key decisions in various domains like healthcare, finance and criminal justice -
biased models may perpetuate discrimination and social injustices.
(i) Improved Data Quality: By setting standards and processes defined in this
framework it improves data accuracy and reliability resulting in better decision-
making.
(iii) Strengthened Data Security: The framework provides controls and protection
measures that safeguard sensitive information against unintended access or
breaches.
(v) Trust and Credibility: Reliable data and ethical practices help build trust
among customers, stakeholders and partners of an organization and improve its
credibility.
(vi) Improved Decision-Making: Accessing accurate and timely data allows leaders
to make more informed and strategic decisions.
When engaging in research that involves dealing with data belonging to another,
several ethical principles should guide its conduct to protect individuals' rights,
privacy, and well-being. Some key ethical guidelines include the following.
(i) Data Anonymity and Privacy: Researchers should take great care in protecting
individual identities while anonymizing data to avoid identification of specific
participants. Adequate security measures must also be implemented to protect
against unauthorized access and breaches in security.
(ii) Beneficence: Researchers should prioritize participant welfare and ensure that
potential benefits outweigh risks when it comes to research projects, which
should strive to contribute positively while minimising harm.
(iii) Nonmaleficence: Researchers must take steps to avoid inflicting physical and
emotional harm on participants through research; this includes conducting
studies that reduce distress while protecting participant safety.
(iv) Transparency and Honesty: Researchers should always be open about their
methods, data collection procedures and any potential conflicts of interest that
might exist in their research. Honest reporting and disclosure of findings is crucial
in maintaining research integrity.
(vi) Social Responsibilty: Researchers should carefully consider the wider social
ramifications of their research, with an aim of meeting society's challenges
responsibly.
(i) Privacy Concerns: Online data collection often involves tracking user behavior
and collecting vast quantities of personal information about them, which may
raise privacy concerns among individuals, necessitating enhanced data protection
measures as well as clear consent mechanisms.
(ii) Data Security: Given the risk of hackers and unauthorized access, strong data
protection in an online environment is of critical importance.
(iv) Scope and Scale: Online research can reach an expansive and wide-reaching
audience, potentially impacting multiple individuals at once. Researchers should
carefully consider their studies' scale as well as any unforeseen outcomes or
implications that may result from them.
(v) Global Reach: Internet research can reach beyond geographical borders to
attract a more diverse participant pool. Researchers must be mindful of cultural
diversity as well as legal considerations that might differ between jurisdictions.
• Consent
• Clarity
• Consistency
• Control
• Consequences
One of the important concepts of ethics in data science is that the individual has
some data ownership. Collecting someone’s personal data without their
agreement is illegal and immoral .As a result, consent is required to acquire
someone’s data.
Voluntary participation
Informed consent
Anonymity
Confidentiality
Potential for harm
Result communication
10. What are the 4 fundamentals of ethics? Or what are the 4 pillars of
ethics?
Beneficence
Nonmaleficence
Autonomy
Justice
Consent is the foundational principle of data ethics. It refers to the idea that
individuals should have the right to provide informed and voluntary consent
before their data is collected, processed or used in any way.