Published January 1, 2022
| Version Version 2.0
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Functional genomics analysis to disentangle the role of genetic variants in major depression - Supplementary Tables
Authors/Creators
- 1. 1 Research Programme on Biomedical Informatics (GRIB), IMIM (Hospital del Mar Medical Research Institute), UPF (Pompeu Fabra University), Dr. Aiguader, Barcelona, Spain
- 2. Research Programme on Biomedical Informatics (GRIB), IMIM (Hospital del Mar Medical Research Institute), UPF (Pompeu Fabra University), Dr. Aiguader, Barcelona, Spain; MedBioinformatics Solutions SL, Almogàvers 165, 08018 Barcelona, Spain
- 3. Laboratorio Internacional de Investigación sobre el Genoma Humano, Universidad Nacional Autónoma de México, Campus Juriquilla, Blvd Juriquilla 3001, Santiago de Querétaro 76230, Mexico
Description
This entry contains the data generated by the study "Functional genomics analysis to disentangle the role of genetic variants in major depression" that are part of the Supplementary information of the article describing the study.
The entry contains the following data:
Supplementary Tables S1-S7
Supplementary Table S1. Summary of resources.
Supplementary Table S2. Causal GVs for MD.
Supplementary Table S3. pGenes functional and disease enrichment analysis.
Supplementary Table S4. Fine-mapped MD causal GVs disease enrichment analysis.
Supplementary Table S5. Colocalizing GWAS-eQTLs association to disease.
Supplementary Table S6. TFBS analysis.
Supplementary Table S7. GVs state annotation.
Notes
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Additional details
Funding
- European Commission
- TransQST - Translational quantitative systems toxicology to improve the understanding of the safety of medicines - Sofia: 116030 116030
- European Commission
- ELIXIR-EXCELERATE - ELIXIR-EXCELERATE: Fast-track ELIXIR implementation and drive early user exploitation across the life-sciences. 676559
- European Commission
- eTRANSAFE - Enhacing TRANslational SAFEty Assessment through Integrative Knowledge Management 777365