There is a Board of Certification for Genealogists and their certification is a highly sought after and difficult to obtain prize! Though I have not chosen to apply for Board Certification at this time, I do adhere to their ethics and standards. Here are the BCG ethics that you should expect from any serious genealogist.
To protect the public
There is a Board of Certification for Genealogists and their certification is a highly sought after and difficult to obtain prize! Though I have not chosen to apply for Board Certification at this time, I do adhere to their ethics and standards. Here are the BCG ethics that you should expect from any serious genealogist.
I will identify my sources for all information and cite only those I have personally used.
I will quote sources precisely, avoiding any alterations that I do not clearly identify as editorial interpretations.
I will present the purpose, practice, scope, and possibilities of genealogical research within a realistic framework.
I will delineate my abilities, publications, and/or fees in a true and realistic fashion.
I will not publish any personal, genealogical, or genetic information disclosed to me unless I have informed consent or omit personally identifying detail. I will also treat publicly available information about living people with sensitivity and will not publish any information with foreseeable potential for harm.
To protect the client (paying or pro bono)
I will reveal to the client any personal or financial interests that might compromise my professional obligations.
I will undertake paid research commissions only after a clear agreement as to scope and fee.
I will, to the best of my abilities, address my research to the issue raised by the client and report to that question.
I will seek from the client all prior information and documentation related to the research and will not knowingly repeat the work as billable hours without explanation as to good cause.
I will furnish only facts I can substantiate with adequate documentation; and I will not withhold any data necessary for the client’s purpose.
If the research question involves analysis of data in order to establish a genealogical relationship or identity, I will report that the conclusions are based on the weight of the available evidence and that absolute proof of genealogical relationships is usually not possible.
If I cannot resolve a research problem within the limitations of time or budget established by contract, I will explain the reasons why.
If other feasible avenues are available, I will suggest them; but I will not misrepresent the possibilities of additional research.
I will return any advance payment that exceeds the hours and expenses incurred.
I will not publish or circulate reports in which a client or colleague has a proprietary interest without that person’s informed consent. I will respect this interest whether my report was made directly to the client or to an employer or agent.
To protect the profession
I will act, speak, and write in a manner I believe to be in the best interests of the profession and scholarship of genealogy.
I will participate in exposing genealogical fraud; but I will not otherwise knowingly injure or attempt to injure the reputation, prospects, or practice of another genealogist.
I will not attempt to supplant another genealogist already employed by a client or agency. I will substitute for another researcher only with specific, written consent of and instructions provided by the client or agency.
I will not represent as my own the work of another. This includes works that are copyrighted, in the public domain, or unpublished. This pledge includes reports, lecture materials, audio/visual tapes, compiled records, and authored essays.
I will not reproduce for public dissemination, in an oral or written fashion, the work of another genealogist, writer, or lecturer without that person’s written consent. In citing another’s work, I will give proper credit.
To protect people who provide DNA samples
When seeking DNA from a living person for genealogical research, I will explain
a) how I would use and share their genetic information and the risks and benefits of that use and sharing;
b) the possibility and consequences of discovering unanticipated relatives, unknown medical conditions, unexpected ethnic backgrounds, and intentional misinformation about such situations;
c) options for openness and privacy, how other researchers could or could not access the data; and why complete anonymity and privacy can never be guaranteed.
After providing this information, I will request and comply with the consent, freely given by the person providing the DNA sample or that person’s guardian or legal representative.
When working with DNA test results of living people, I will not publish personally identifying information without each test taker’s consent. I will not privately share a match list without the list owner’s consent. If I have the list owner’s consent, I may privately share details of a match without the match’s consent.
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