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Autor:
Charles E. Breeze, Eric Haugen, Alex Reynolds, Andrew Teschendorff, Jenny van Dongen, Qing Lan, Nathaniel Rothman, Guillaume Bourque, Ian Dunham, Stephan Beck, John Stamatoyannopoulos, Nora Franceschini, Sonja I. Berndt
Publikováno v:
Genome Biology
Genome Biology, Vol 23, Iss 1, Pp 1-22 (2022)
Genome Biology, 23:13, 1-22. Springer Verlag
Breeze, C E, Haugen, E, Reynolds, A, Teschendorff, A, van Dongen, J, Lan, Q, Rothman, N, Bourque, G, Dunham, I, Beck, S, Stamatoyannopoulos, J, Franceschini, N & Berndt, S I 2022, ' Integrative analysis of 3604 GWAS reveals multiple novel cell type-specific regulatory associations ', Genome Biology, vol. 23, 13, pp. 1-22 . https://doi.org/10.1186/s13059-021-02560-3
Genome Biology, Vol 23, Iss 1, Pp 1-22 (2022)
Genome Biology, 23:13, 1-22. Springer Verlag
Breeze, C E, Haugen, E, Reynolds, A, Teschendorff, A, van Dongen, J, Lan, Q, Rothman, N, Bourque, G, Dunham, I, Beck, S, Stamatoyannopoulos, J, Franceschini, N & Berndt, S I 2022, ' Integrative analysis of 3604 GWAS reveals multiple novel cell type-specific regulatory associations ', Genome Biology, vol. 23, 13, pp. 1-22 . https://doi.org/10.1186/s13059-021-02560-3
Background Genome-wide association study (GWAS) single nucleotide polymorphisms (SNPs) are known to preferentially co-locate to active regulatory elements in tissues and cell types relevant to disease aetiology. Further characterisation of associated