|
About the Open Targets Genetics FAQs category
|
|
0
|
356
|
25 April 2021
|
|
What is the best way to query pheWAS traits for multiple variants?
|
|
5
|
787
|
10 August 2023
|
|
Why does Open Targets Genetics display partial L2G scores on Locus pages when there is no evidence of colocalization?
|
|
0
|
539
|
3 November 2021
|
|
Why are beta and odds ratios not always displayed in Open Targets Genetics?
|
|
0
|
1332
|
26 August 2021
|
|
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?
|
|
0
|
459
|
23 August 2021
|
|
How can I download data from Open Targets Genetics?
|
|
0
|
1422
|
4 August 2021
|
|
How often is Open Targets Genetics updated?
|
|
0
|
489
|
29 July 2021
|
|
In Open Targets Genetics, what is the “credible set overlap”?
|
|
0
|
940
|
22 July 2021
|
|
How to interpret Variant-to-Gene (V2G) and Locus-to-Gene (L2G) scores in Open Targets Genetics
|
|
0
|
1680
|
19 July 2021
|
|
What fine-mapping and colocalisation software does Open Targets Genetics use?
|
|
0
|
540
|
14 July 2021
|
|
How are tag variants identified in Open Targets Genetics?
|
|
0
|
558
|
12 July 2021
|
|
How are UK Biobank study traits identified in Open Targets Genetics?
|
|
0
|
466
|
7 July 2021
|
|
What do scores represent in downloaded tables of eQTL data for query variants
|
|
1
|
247
|
4 January 2023
|
|
Beta values in study colocalisation table of study locus page
|
|
2
|
380
|
17 November 2022
|
|
Conserved regions variants
|
|
2
|
358
|
27 July 2022
|
|
Which version of GTEx does Open Targets Genetics use for colocalization analysis?
|
|
1
|
456
|
20 May 2022
|
|
How was LD clumping performed to select eQTLs for candidate gene?
|
|
3
|
368
|
11 May 2022
|
|
Where to find eQTL information regarding a SNP in Open Targets Genetics?
|
|
1
|
536
|
21 March 2022
|
|
Empty results pages
|
|
6
|
394
|
10 March 2022
|
|
How are rsIDs mapped to unique variants in Open Targets Genetics?
|
|
1
|
833
|
1 March 2022
|