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I am planning to use Coloc for identifying shared genetic signals for two EQTL-GWAS studies.
Given that the reference genome used in EQTL data is GRCh38, while many GWAS data use GRCh37 as the reference genome, I would like to inquire whether colocalization analysis require chromosome (chr) and base pair (bp) information, and whether a uniform reference genome is needed if so.
Looking forward to your reply. Thank you for your assistance!
Russell
The text was updated successfully, but these errors were encountered:
Somehow you will need to match up the SNPs from the two studies. If you can use rs IDs, that's fine. But coloc will not do liftover itself.
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Subject: [chr1swallace/coloc] whether COLOC analysis require CHR and BP information (Issue #173)
Hi all,
I am planning to use Coloc for identifying shared genetic signals for two EQTL-GWAS studies.
Given that the reference genome used in EQTL data is GRCh38, while many GWAS data use GRCh37 as the reference genome, I would like to inquire whether colocalization analysis require chromosome (chr) and base pair (bp) information, and whether a uniform reference genome is needed if so.
Looking forward to your reply. Thank you for your assistance!
Russell
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Hi all,
I am planning to use Coloc for identifying shared genetic signals for two EQTL-GWAS studies.
Given that the reference genome used in EQTL data is GRCh38, while many GWAS data use GRCh37 as the reference genome, I would like to inquire whether colocalization analysis require chromosome (chr) and base pair (bp) information, and whether a uniform reference genome is needed if so.
Looking forward to your reply. Thank you for your assistance!
Russell
The text was updated successfully, but these errors were encountered: