How to retrieve & compare study-specific GWAS variant lists (e.g., UKB vs FinnGen) for a phenotype?
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1
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33
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8 May 2025
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Missing variant from previous Open Targets Genetics Platform
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5
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60
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24 April 2025
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25.03 Platform release now live! Open Targets Genetics data update
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2
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120
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28 March 2025
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Data sources for V2G Scoring
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5
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37
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13 March 2025
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Where to find summary statistics for QTL studies (and through API)?
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7
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434
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28 February 2025
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Single variant PheWAS result are not able to download?
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1
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26
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20 December 2024
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Full summary statistics
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3
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66
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5 December 2024
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Open Targets Genetics local setup
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1
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37
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14 October 2024
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What's the plan to integrate DepMap?
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2
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233
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20 August 2024
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Variant to Gene Query for multiple variants in OT Genetics
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4
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527
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20 August 2024
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Get V2G genes/scores from variant rsid?
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7
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670
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20 August 2024
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Manhattan data interpretation
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1
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35
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5 July 2024
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Deploying Open Targets Genetics using Terraform
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1
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59
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26 June 2024
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Inheritance model (Dominant, Recessive etc) in ClinVar and Genomics England
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0
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55
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20 May 2024
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Data source scores ot_genetics_portal vs L2G in final association score
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1
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84
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8 May 2024
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GWAS Catalog results incorporation - backlog or other issue?
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2
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146
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19 April 2024
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FH Alzheimer disease dementia custom
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0
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80
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21 March 2024
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L2G Scoring Pipeline Implementation
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5
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383
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14 March 2024
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Are OpenTargets in collaboration with All of Us?
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2
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111
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26 February 2024
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Next update for https://genetics.opentargets.org/
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1
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213
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8 December 2023
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L2G JSON download for Open Targets Genetics
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4
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276
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7 December 2023
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UKB-PPP data: UK Biobank Pharma Proteomics Project
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4
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372
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29 November 2023
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Difference between variant and gene pages
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2
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215
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23 November 2023
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Large-scale rare variant burden testing in Parkinson's disease
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1
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238
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14 November 2023
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Do you plan to integrate TWAS into Open Targets Genetics?
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3
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378
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7 November 2023
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Category variable related association from Genebass-UKB project
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0
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133
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2 November 2023
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Direction of the effect size in Associated studies: Colocalisation analysis section
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2
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226
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2 November 2023
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Open Targets Genetics 2023 data release
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1
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248
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23 October 2023
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Inferring direction of therapeutic effect implied by coding genetic evidence
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5
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293
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23 October 2023
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Getting signs of GWAS effects relative to major alleles instead of alt alleles
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5
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331
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19 October 2023
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