Open Shrishtee-kandoi opened 8 months ago
P values are NA or invalid.
Sam
On Tue, Feb 27, 2024 at 6:47 PM Shrishtee kandoi @.***> wrote:
Assigned #352 https://github.com/choishingwan/PRSice/issues/352 to @choishingwan https://github.com/choishingwan.
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I just checked and did not find any NA values. Could you tell what the criteria for invalid p-values is?
The range of p-values is: [1] 1.937e-110 1.000e+00
7227799 variant(s) observed in base file, with: 7227799 NA stat/p-value observed
Try and see if 2.3.5 handle this better. I vaguely remember old versions have problem with scientific values. As long as the p value is more than 1e-231 then 2.3.5 should in theory handle that
Sam
On Tue, Feb 27, 2024 at 6:53 PM Shrishtee kandoi @.***> wrote:
I just checked and did not find any NA values. Could you tell what the criteria for invalid p-values is?
The range of p-values is: [1] 1.937e-110 1.000e+00
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Is there a different way to upgrade to 2.3.5? I cloned the repository from Github only a few weeks and also did it again right now but it gives me the same error.
I also had another question (may not be relevant to this): Is it possible to run a PRS without stats and/or A1,A2 values? Because a lot of GWASes don't give out those information..
We were at 2.3.5 since I left academic in 2022. Maybe you can try and download the binaries?
You meant running a PRS? You can’t run PRS without effect sizes or the effective allele
Sam
On Tue, Feb 27, 2024 at 7:07 PM Shrishtee kandoi @.***> wrote:
Is there a different way to upgrade to 2.3.5? I cloned the repository from Github only a few weeks and also did it again right now but it gives me the same error.
I also had another question (may not to relevant to this): Is it possible to run a GWAS without stats and/or A1,A2 values? Because a lot of GWASes don't give out those information..
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Yes, I meant PRS sorry! Thanks. I will try downloading that.
Dear Author,
I am trying to run PRS but keep getting this error:
Error: No valid variant remaining
PRSice 2.3.3 (2020-08-05) https://github.com/choishingwan/PRSice (C) 2016-2020 Shing Wan (Sam) Choi and Paul F. O'Reilly GNU General Public License v3 If you use PRSice in any published work, please cite: Choi SW, O'Reilly PF. PRSice-2: Polygenic Risk Score Software for Biobank-Scale Data. GigaScience 8, no. 7 (July 1, 2019) 2024-02-27 18:36:56 ./PRSice_linux \ --a1 ref \ --a2 alt \ --bar-levels 0.001,0.05,0.1,0.2,0.3,0.4,0.5,1 \ --base GWAS_file.gz \ --base-maf MAF:0.01 \ --binary-target F \ --bp pos \ --chr chrom \ --clump-kb 250kb \ --clump-p 1.000000 \ --clump-r2 0.100000 \ --interval 5e-05 \ --lower 5e-08 \ --num-auto 22 \ --or \ --out Output_file \ --pheno phenofile \ --print-snp \ --pvalue p_value \ --seed 2360945017 \ --snp rsid \ --stat beta \ --target target_file \ --thread 1 \ --upper 0.5
Warning: MAF field not found in base file. Will not perform MAF filtering on the base file
Initializing Genotype file: target_file (bed)
Start processing GWAS_file ==================================================
Base file: GWAS_file.gz GZ file detected. Header of file is:
rsid chrom pos ref alt neg_log_pvalue beta stderr_beta alt_allele_freq p_value
7227799 variant(s) observed in base file, with: 7227799 NA stat/p-value observed 0 total variant(s) included from base file
Error: No valid variant remaining
Would you please be able to help? Is there something that I'm missing?