Hi,
thanks very much for developing this repo!
I was wondering how were the negative set of variants selected for eQTLs exactly.
I downloaded the finemapping table ("GTEx_49tissues_release1.tsv.bgz") from the Finucane lab (https://www.finucanelab.org/data), and I was able to reproduce the set of positive variants, setting a PIP threshold of 0.9.
However, although all your negative variants are in the table, I cannot prioritize them:
- I consider only variants with PIP < 0.01
- I compute TSS distances to target genes of positive variants
- For each positive variant, I select the negative variant with the most similar TSS distance to the same target gene
Thanks very much in advance for your help! Best,
Miquel
Hi,
thanks very much for developing this repo!
I was wondering how were the negative set of variants selected for eQTLs exactly.
I downloaded the finemapping table ("GTEx_49tissues_release1.tsv.bgz") from the Finucane lab (https://www.finucanelab.org/data), and I was able to reproduce the set of positive variants, setting a PIP threshold of 0.9.
However, although all your negative variants are in the table, I cannot prioritize them:
Thanks very much in advance for your help! Best,
Miquel