Genomics for Aotearoa New Zealand

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Where society and genomics science meet!

Genomics for Aotearoa New Zealand is a charitable incorporated society focused on the benefits of genomics for everyone. Genomics is the study of all or most of the DNA of living things. This kind of science has broad reach including: human health, ecology, agriculture, horticulture, climate change monitoring, and more.

Our purposes:

  1. To promote, research, develop, and apply genomics for the benefit of all society;
  2. To promote and support Te Ao Māori and Te Tiriti o Waitangi as innate to New Zealand genomics;
  3. To promote and support collaboration on genomics within New Zealand and internationally, cognisant of the 61/295 United Nations Declaration on the Rights of Indigenous Peoples;
  4. To promote and support education and public engagement in the field of genomics;
  5. To promote and support collaboration between genomics and a variety of disciplines;
  6. To provide guidance to stakeholders in regards to genomics.

Our History:

The ideas behind GFANZ were put together in a concept business plan for MBIE's call for an Advanced Genomics Research Platform in 2016. The team expected MBIE to go with the big incumbents, so their aim was different. It was to put forth a modern, nimble, Aotearoa specific proposal with ideas that anyone could then use. With that in mind the team published it under a CC-BY license at their first web site. You can see that archived work here:

GFANZ founders recognised that many of the ideas in that concept business plan could be made real without funding. They then took the steps necessary to start the incorporated society as described in the document they wrote for MBIE. The society launched in late 2017 and became a charitable organisation in 2020.

GFANZ has been about addressing big challenges from the beginning. We often find that the things that really need doing have been put in the too hard basket. Things like suitable career pathways for early career researchers and opportunities for equitable participation in the review and renewal of the national research, science, and innovation system. The council's decision to put our name and effort into this community is one way we are working to affect positive, impactful change in Aotearoa.

We collaborate with other like minded organisations, such as the Indigenous Genomics Institute and the New Zealand Association of Scientists, knowing that we can do more together, and learn so much from one another.

To find our more about GFANZ or to become a member, visit our website at

The safety and control of human genetic / genomic data is critically important. The for profit corporate model has some issues as this article discusses. GFANZ is preparing to look at the current state of law around this kind of data in Aotearoa. This way we can help inform people as they choose whether or not / how / with whom to trust their data.

Running a not-for-profit or charitable society? Wondering were to find official guidance regarding income and taxes? Below is the go to site by the IRD for these things.‍

Genomics for Aotearoa New Zealand (GFANZ) is the parent organisation of Te Ara Paerangi Community.

We had our AGM last night. It all went smoothly. How could it not with this great group of people! In addition to the usual required agenda items, we voted to accept the updated constitution. This is brings us up to date with the Incorporated Societies act of 2022 and adds one more object:

To promote and support collaboration between genomics and a variety of disciplines;

We are well aware of how broadly genomics touches peoples lives and the world around us. As a research discipline, genomics can inform what we can do. But can and should are different things. The should needs to be determined by societal discussions deeply informed by other disciplines and epistemologies. While GFANZ has always been a collaborative organisation, we wanted to make that explicit in our core objectives.

Now we have.

Along with updating our constitution, we have just launched a new membership management system and web site. It is now super easy to join with a range of affordable subscription options.

If you appreciate what we do here, please join now.

Better technology is making it easier and cheaper to access biodiversity genomic data. Managing this data properly is important, but there's still confusion about the best way to do it. The authors offer guidance on how to handle this data well.

Incorporated Societies and Charitable Trusts may find this resource helpful.

The Societies Act of 1908 has been updated to the Societies Act of 2022. We have been going through the process of updating our constitution and operating processes to comply with the new act. We collected the list of resources below as we did that work. Your society might find them helpful as you update your society to comply with the new act.

Those who have already made the transition to using AI are reaping the benefits of vastly accelerated workflows and targeted decision-making in data analysis. But for bioinformaticians who remain on the fence, there are challenges to consider when taking the leap.

‍ Using AI in bioinformatics is on the agenda for a Palmy Bioinfo meeting next year. Lots to discuss, from the practical 'How do you do this' to the ethics of code scraping against software licenses. Quite interesting the Nature is suggesting that people get on the bandwagon or experience FOMO.

Jonathan Pritchard of Stanford University has released the first half (still writing the second) of his textbook on human genomics. It is licensed under CC-BY-4.0 Creative Commons License.

Quote from his site:

In this book I describe the forces that govern genetic variation including mutation, drift, recombination and selection, as well as what genetics teaches us about human history, and the role of genetic variation in human phenotypes and diseases. When complete, the book will combine the three pillars of human population genetics - population genetics, population history, and trait genetics - under a single umbrella, with a focus on examples and applications in human genetics. Moreover, each section emphasizes the essential interplay between theory, statistical methods, and biological applications, with a focus on building intuition while avoiding heavy technical detail where possible.
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