PhenomeXcan: Mapping the genome to the phenome through the transcriptome

Data generated as part of the PhenomeXcan project, which contains processed results for S-MultiXcan, S-PrediXcan, fastENLOC and the integration of S-MultiXcan results with ClinVar. Please, refer to the Github repository for documentation on these files and related source code (https://github.com/hakyimlab/phenomexcan). This latest version of the dataset contains the fixed results for fastENLOC (with shrinkage of alpha1 values). bioRxiv preprint: https://doi.org/10.1101/833210本数据集为PhenomeXcan项目的产出数据，包含S-MultiXcan、S-PrediXcan、fastENLOC的处理后结果，以及S-MultiXcan分析结果与临床变异数据库（ClinVar）的整合内容。相关文件及源代码的文档说明，请参阅其GitHub仓库：https://github.com/hakyimlab/phenomexcan。本数据集的最新版本包含了针对fastENLOC的修正结果（已对alpha1值进行收缩处理）。相关预印本已发布于bioRxiv：https://doi.org/10.1101/833210