International groundbreaking genetic ALS research

To understand the genetic basis of ALS and to ultimately find a cure for this devastating, fatal neuromuscular disease, Project MinE aims to analyse the DNA of at least 15,000 ALS patients and 7,500 controls. The resulting 22,500 DNA profiles will be compared.

33%
10,904 / 22,500
DNA profiles collected
Make it yours. Donate now
Project MinE: a unique worldwide collaboration! Read more
Our initiators explain Project MinE. Watch video
Two new ALS genes Read here
Start a campaign! Start here
Project MinE meeting: >10,000 DNA profiles Read here

Make a donation today

100 percent of all donations to Project Mine will go directly towards the mapping and analysis of DNA profiles.

Project MinE: Make it yours!

Help us raise more funds by starting your own campaign. Need inspiration? Check out the current campaigns.

Milestones

Project MinE twitter

today
  • 04.12.2020
    5th Project MinE Science Meeting – virtual
    04.12.2020
    5th Project MinE Science Meeting – virtual

    Researchers meet and discuss their progress on data mining activities in Project MinE with the genomes so far.

    ×
  • 09.12.2020
    31st International Symposium on ALS/MND virtually, 9-11 December 2020
    09.12.2020
    31st International Symposium on ALS/MND virtually, 9-11 December 2020

    Researchers from all over the world meet virtually to discuss their latest results, share ideas and start up more collaborations.

    More information: symposium.mndassociation.org

    ×
  • 11.12.2020
    2020 Healey Center International Prize for Innovation in ALS awared to Project MinE
    11.12.2020
    2020 Healey Center International Prize for Innovation in ALS awared to Project MinE

    This global prize recognizes excellence in research for a team whose efforts have catalyzed exceptional discoveries leading to a transformative advance in therapy development in ALS, collectively making an impact in ALS.

    ×

Our partners