Summary Statistics: Assessing the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases
Creators
Contributors
Researchers:
- Camacho, Niedzica
- Shea, Patrick
- Stopsack, Konrad
- Joseph, Vijai
- Burren, Oliver
- Dhindsa, Ryan
- Nag, Abhishek
- Berchuck, Jacob
- O'Neill, Amanda
- Abbasi, Ali
- Zoghbi, Anthony
- Alegre-Díaz, Jesus
- Kuri-Morales, Pablo
- Berumen, Jaime
- Tapia-Conyer, Roberto
- Emberson, Jonathan
- Torres, Jason
- Collins, Rory
- Wang, Quanli
- Goldstein, David
- Matakidou, Athena
- Haefliger, Carolina
- Anderson-Dring, Lauren
- March, Ruth
- Jobanputra, Vaidehi
- Dougherty, Brian
- Carss, Keren
- Petrovski, Slavé
- Kantoff, Philip
- Offit, Kenneth
- Mucci, Lorelei
- Pomerantz, Mark
- Fabre, Margarete
Description
Exome-wide gene and single variant level summary statistics associated with the Nature Communications article "Assessing the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases".
Gene Level Association Files
- gene_level_prostate_cancer_risk.txt: Gene-level summary statistics for association with prostate cancer risk (case vs controls)
- gene_level_prostate_cancer_severity.txt: Gene-level summary statistics for association with prostate cancer severity (aggressive prostate cancer vs non-aggressive prostate cancer)
- gene_level_prostate_cancer_agg_ctrl.txt: Gene-level summary statistics for association of aggressive prostate cancer vs controls
Columns
- Gene Name
- Gene ENSG - Ensembl gene ID
- CA_model - collapsing analysis qualifying variant model (as in Supplementary Data 1 of article)
- CMH_P - meta analysis P-value
- CMH_OR - meta analysis odds ratio
- CMH_OR_LCI - meta analysis odds ratio lower confidence interval
- CMH_OR_UCI - meta analysis odds ratio upper confidence interval
- Total Qual Cases - number of cases carrying a qualifying variant
- Total Unqual Cases - number of cases not carrying a qualifying variant
- Total Qual Ctrls - number of controls carrying a qualifying variant
- Total Unqual Ctrls - number of controls not carrying a qualifying variant
Single Variant Level Association File
- single_variant_prostate_cancer_risk.txt: Single variant level summary statistics for association with prostate cancer risk (case vs controls)
Columns
- chr - chromosome
- pos - genomic position
- effect_allele
- other_allele
- P - meta analysis P-value
- direction - direction of effect in individual cohorts (100KGP, MCPS, UKB_SAS, UKB_AFR, UKB_EUR, FinnGen)