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About the Open Targets Genetics FAQs category
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0
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345
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25 April 2021
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What is the best way to query pheWAS traits for multiple variants?
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5
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623
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10 August 2023
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Why does Open Targets Genetics display partial L2G scores on Locus pages when there is no evidence of colocalization?
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0
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503
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3 November 2021
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Why are beta and odds ratios not always displayed in Open Targets Genetics?
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0
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1313
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26 August 2021
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In the “tag variants” section of variant summary pages in Open Targets Genetics, why do some SNPs have a posterior probability and others don’t?
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0
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443
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23 August 2021
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How can I download data from Open Targets Genetics?
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0
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1303
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4 August 2021
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How often is Open Targets Genetics updated?
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0
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461
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29 July 2021
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In Open Targets Genetics, what is the “credible set overlap”?
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0
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900
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22 July 2021
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How to interpret Variant-to-Gene (V2G) and Locus-to-Gene (L2G) scores in Open Targets Genetics
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0
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1311
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19 July 2021
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What fine-mapping and colocalisation software does Open Targets Genetics use?
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0
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505
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14 July 2021
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How are tag variants identified in Open Targets Genetics?
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0
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536
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12 July 2021
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How are UK Biobank study traits identified in Open Targets Genetics?
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0
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441
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7 July 2021
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What do scores represent in downloaded tables of eQTL data for query variants
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1
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231
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4 January 2023
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Beta values in study colocalisation table of study locus page
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2
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339
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17 November 2022
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Conserved regions variants
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2
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327
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27 July 2022
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Which version of GTEx does Open Targets Genetics use for colocalization analysis?
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1
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433
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20 May 2022
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How was LD clumping performed to select eQTLs for candidate gene?
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3
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345
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11 May 2022
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Where to find eQTL information regarding a SNP in Open Targets Genetics?
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1
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432
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21 March 2022
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Empty results pages
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6
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326
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10 March 2022
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How are rsIDs mapped to unique variants in Open Targets Genetics?
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1
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694
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1 March 2022
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