Chris Ponting – Datasets — University of Edinburgh Research Explorer

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Disease-causal DNA variants; ME/CFS genetics; machine learning; thymus single cell biology

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Protein genome-wide associations from the paper 'Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits'.
Vitart, V. (Creator), Hayward, C. (Creator), Wilson, J. (Creator), Tenesa, A. (Creator), Ponting, C. (Creator), Baillie, K. (Creator), Haley, C. (Creator), Amador, C. (Creator), Bretherick, A. (Creator), Canela Xandri, O. (Creator), Joshi, P. (Creator), Clark, D. W. (Creator), Rawlik, K. (Creator), Boutin, T. (Creator), Zeng, Y. (Creator), Navarro, P. (Creator), Rudan, I. (Creator), Wright, A. F. (Creator) & Campbell, H. (Creator), Edinburgh DataShare, 16 Jun 2020
DOI: 10.7488/ds/2838, https://doi.org/10.1371/journal.pgen.1008785
Dataset
DecodeME Questionnaire
Ponting, C. (Creator), Baker, T. (Creator) & Garcia, D. (Creator), Edinburgh DataShare, 7 Apr 2023
DOI: 10.7488/ds/3836, https://doi.org/10.1186/s12883-022-02763-6
Dataset