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About the GraphQL API category
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0
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423
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25 April 2021
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List of commands and options available in OTG GraphQL for running PheWAS
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6
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121
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8 March 2024
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R script for GraphQL query: query targetDiseaseEvidence
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7
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781
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11 January 2024
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Retrieving >25 associated drugs
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2
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192
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6 September 2023
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How to modify data source weights in the API?
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3
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301
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23 August 2023
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GraphQL and API downloads
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4
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237
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14 August 2023
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Sample R script to query GraphQL API
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5
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628
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11 August 2023
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An R script to use API for fetching "Associated studies: locus-to-gene pipeline" section for a gene
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3
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376
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11 August 2023
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Can we get all Bibliography data per gene using the api?
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5
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286
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19 July 2023
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Date of access using API
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1
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185
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13 June 2023
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R script for GraphQL query: query multiple rsID and get gene IDs and Annotation information
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17
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368
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18 May 2023
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Query to retrieve studyID from variants not working
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1
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298
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11 May 2023
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Downloading variant information
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7
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719
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2 May 2023
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Data source scores
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1
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221
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2 May 2023
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Accessing locus-to-gene (L2G) and colocalisation data from Open Targets Genetics by querying the API using Python
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0
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717
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3 June 2021
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Query all snps associated with a disease
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1
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257
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20 March 2023
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Query by GeneID and Phenotype to get L2G scores
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1
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217
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15 March 2023
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BFilter does't work
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1
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184
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13 March 2023
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Number of Manhattan lead variants does not match numAssocLoci from API
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0
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165
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2 March 2023
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L2G results missing via API and web
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0
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197
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2 March 2023
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Accessing PCHi-C, DHS-promoter corr. etc. info via Open Targets Genetics GraphQL API
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2
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196
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9 February 2023
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Extensible GraphQL API Template for Serving Custom Data
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1
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212
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27 January 2023
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How to guide ... accessing drug warning and pharmacovigilance data
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1
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470
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17 January 2023
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Retrieving all targets associated with a disease using the API (pagination)
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1
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340
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11 January 2023
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Get associations from different ids
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1
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232
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4 January 2023
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Can I load my sumstats or loci to perform Locus-to-gene annotation?
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1
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243
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23 November 2022
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Issue with "studiesForGene" graphql query
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1
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271
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7 November 2022
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studiesAndLeadVariantsForGene query not working
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4
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372
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7 November 2022
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Retrieving >50 pathways from evidences
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4
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565
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22 September 2022
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PheWAS / GWAS lead variants & Tag variants query for multiple snps
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1
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434
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31 August 2022
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