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Whole_genome_sequencing_of_Crohn_s_disease_patients

Population based sequencing of whole genomes of Crohn's disease patients.

Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data

Dataset ID Description Technology Samples
EGAD00001000117 Illumina Genome Analyzer II Illumina HiSeq 2000 152
EGAD00001000401 Illumina HiSeq 2000 2926
Publications Citations
Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7.
Nat Genet 49: 2017 186-192
88
Leveraging functional annotations in genetic risk prediction for human complex diseases.
PLoS Comput Biol 13: 2017 e1005589
89
Joint modeling of genetically correlated diseases and functional annotations increases accuracy of polygenic risk prediction.
PLoS Genet 13: 2017 e1006836
39
Identifying Crohn's disease signal from variome analysis.
Genome Med 11: 2019 59
13
Leveraging effect size distributions to improve polygenic risk scores derived from summary statistics of genome-wide association studies.
PLoS Comput Biol 16: 2020 e1007565
21