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3 votes
1 answer
120 views

How to perform liftover from 38 to 37 in R?

I have some gwas summary statistics in GRCh38 that I want to lift to GRCh37. I am trying to liftover in R using this code: ...
DN1's user avatar
  • 85
0 votes
1 answer
645 views

Identify SNP from genetic position

I am looking for a way to obtain SNP names from their coordinates (Chromosome:BP) - very much the reverse of the question answered here: (https://stackoverflow.com/questions/20251612/map-snp-ids-to-...
Gux's user avatar
  • 103
2 votes
0 answers
56 views

LD block labels annotation for GWAS summary data

I have a txt file summarising the result of a GWAS on an European population. Its structure is the next one: ...
Gero's user avatar
  • 73
3 votes
1 answer
647 views

How to estimate the phenotypic variation explained by top SNPs from a GWAS study?

I have conducted a large-scale GWAS study and got a few significantly associated SNPs. I used GEMMA with -lmm 1 options to run ...
Anik Dutta's user avatar
2 votes
1 answer
673 views

how do I convert a vcf file for a GWAS study (using R package vcfR)

I have a vcf file with individual level genetic data, that I read using the R package vcfR ...
spore234's user avatar
  • 121
6 votes
0 answers
107 views

making my own population allele frequency table for input to IADMIX from Gnomad data (population admixture)? [closed]

Hi I'm a first time user of IADMIX. I tested on one known Finnish sample from the 1000Genome project using the softwares provided frequency table hapmap3.8populations.hg19.freqs and the prediction is ...
Sam's user avatar
  • 61