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Abnormal output of SAIGE step 2 with "idstoIncludeFile" parameter #393
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Hi Xiangyu, Thanks for reporting the issue. I think the current bioconda version has the query issue. Could you please try to install SAIGE locally? Thanks, |
@XiangyuYe could you provide exact package versions with build numbers from conda? I need little bit more than: Example how to list those:
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It returns me as follows:
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Hi all! The program will be maintained by multiple SAIGE developers there. Please feel free to try the version 1.0.0 and report issues if any. Thanks! |
Hi Wei,
I tried to use SAIGE to conduct a single variant association test. However, when I used the "idstoIncludeFile" parameter to focus on a subset of variants (with 10 variants for example), it returned me a confusing output with 1 variant repeating 10 times.
I conducted this analysis with R-SAIGE on bioconda, as introducted in #272. The version of SAIGE is "0.44.6.4".
My code is:
step2_SPAtests.R
--bgenFile=${BGENFILE}
--bgenFileIndex=${BGENFILEINDEX}
--idstoIncludeFile=${IDSTOINCLUDEFILE}
--chrom=${chr}
--minMAF=0.0001
--minMAC=1
--LOCO=FALSE
--sampleFile=${sampleIDindosage}
--GMMATmodelFile=${output1}.rda
--varianceRatioFile=${output1}.varianceRatio.txt
--SAIGEOutputFile=${output2}.SAIGE.bgen.genotype.txt
--numLinesOutput=1
--IsOutputAFinCaseCtrl=TRUE
My input of idstoIncludeFile looks like:
rs9617528
rs715549
rs9617160
rs2186521
rs2027649
rs4911642
rs6010418
rs140378
rs131560
rs7287144
The output file looks like (the remaining lines are all the same as this one):
CHR POS SNPID Allele1 Allele2 AC_Allele2 AF_Allele2 imputationInfo N BETA SE Tstat p.value p.value.NA Is.SPA.converge varT varTstar AF.Cases AF.Controls
22 16061016 22:16061016_T_C T C 158035.882353002 0.254201221100026 0.366613502966512 310848 -0.0079956036716851 0.0756549705372079 -1.39693540890738 0.915832196899293 0.915832196899293 1 174.712938042984 178.070185525266 0.253752956435493 0.254203081852324
I appreciate if you could help me fix this. Thank you!
Best regards,
Xiangyu Ye
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