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Error: No valid variant remaining #352
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P values are NA or invalid.
Sam
…On Tue, Feb 27, 2024 at 6:47 PM Shrishtee kandoi ***@***.***> wrote:
Assigned #352 <#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: |
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 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. |
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?
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