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One of my GWAS sum stat files provides a frequency column for the alt allele, and the other provides the allele frequency for allele 1 (which I assume is the reference allele - I'm going to attempt to confirm that). Can I just provide both of these frequency to columns to munge_sumstats.py like I did below? Or do I need to convert the frequency column in one of the summary stats files so that is consistent with the other?
Hello,
One of my GWAS sum stat files provides a frequency column for the alt allele, and the other provides the allele frequency for allele 1 (which I assume is the reference allele - I'm going to attempt to confirm that). Can I just provide both of these frequency to columns to munge_sumstats.py like I did below? Or do I need to convert the frequency column in one of the summary stats files so that is consistent with the other?
Thank you!
python /mnt/mfs/hgrcgrid/homes/nrr2132/ldsc/munge_sumstats.py
--sumstats /mnt/mfs/hgrcgrid/homes/nrr2132/analysis/AAGWAS/11.18.22/WithIbadan/METAL/Model2/ADGC_AA_GWAS3.AGR.MODEL2.with_ibadan.annotated.METAL.20221116_TabSeparated.txt
--N 9095
--snp MarkerName
--a1 Allele1
--a2 Allele2
--p P-value
--frq Freq1
--signed-sumstats Effect,0
--out ADGC_AFR_WithIbadan_Model2_SumStats_Munge.txt
python /mnt/mfs/hgrcgrid/homes/nrr2132/ldsc/munge_sumstats.py
--sumstats /mnt/vast/hpc/reitz_lab/REITZ_LAB/VascularTrait_SummaryStat/Lipids_GWAS_SummaryStats/Global_Lipids_Genetics_Consortium/Graham_2021/African/nonHDL_INV_AFR_HRC_1KGP3_others_ALL.meta.singlevar.results
--N 99432
--snp rsID
--a1 REF
--a2 ALT
--p pvalue
--frq POOLED_ALT_AF
--signed-sumstats EFFECT_SIZE,0
--out nonHDL_Graham2021_AFR_SumStats_munge.txt
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