Science has a history of treating Black Americans and other minority ancestry groups badly. We, as genetics scientists, are working hard to make it right & ensure research also benefits ancestry minorities. a thread #BlackLivesMatter #blackinstem #IndigenousLivesMatter
To do that, we are asking and inviting minority ancestry groups to join genetics research studies (that also include majority ancestry groups fyi). We are dedicated to (and good at) protecting confidentiality and ensuring anonymity. 2/6
But we can't study diseases present in minority ancestry groups if we don't recruit research participants who have these diseases. And we also need to study people without these diseases for comparison. 3/6
We also can't do a good job of predicting and preventing disease in minority ancestry groups if we haven't recruited these individuals for research. 4/6
Help us prevent disease in all people (and not just majority ancestry groups). Join research studies. Donate your DNA to help others (which will especially help others from your own ancestry) 5/6
If you are a University of Michigan @umichmedicine patient, contact us to donate a blood sample to help others, and help us prevent disease. umcvc.org/cardiovascular… #CHIPstudyUM /end
I should add that we are also improving representation of diverse ancestries in the trainees and research team who work on these studies. The recruitment team develops clinical research experience, typically before going to med school. Important that all have access.

• • •

Missing some Tweet in this thread? You can try to force a refresh
 

Keep Current with Cristen Willer, PhD

Cristen Willer, PhD Profile picture

Stay in touch and get notified when new unrolls are available from this author!

Read all threads

This Thread may be Removed Anytime!

PDF

Twitter may remove this content at anytime! Save it as PDF for later use!

Try unrolling a thread yourself!

how to unroll video
  1. Follow @ThreadReaderApp to mention us!

  2. From a Twitter thread mention us with a keyword "unroll"
@threadreaderapp unroll

Practice here first or read more on our help page!

More from @cristenw

Mar 23
If you see saddlepoint approximation used in genomics, @weizhouw introduced the concept to fellow @UMich grad student @ellenmschmidt ~2012/2013 when we developed GREGOR - a method for assessing significance of enrichment of overlap between a genomic feature and GWAS hits
This allowed us to avoid deep permutation to estimate really small (significant) p-values
SPA was introduced by Daniels 1954, building on the work of steepest descent by Debye, Watson, Darwin (the grandson) & Fowler
projecteuclid.org/journals/annal…
Read 7 tweets

Did Thread Reader help you today?

Support us! We are indie developers!


This site is made by just two indie developers on a laptop doing marketing, support and development! Read more about the story.

Become a Premium Member ($3/month or $30/year) and get exclusive features!

Become Premium

Don't want to be a Premium member but still want to support us?

Make a small donation by buying us coffee ($5) or help with server cost ($10)

Donate via Paypal

Or Donate anonymously using crypto!

Ethereum

0xfe58350B80634f60Fa6Dc149a72b4DFbc17D341E copy

Bitcoin

3ATGMxNzCUFzxpMCHL5sWSt4DVtS8UqXpi copy

Thank you for your support!

Follow Us on Twitter!

:(