Yes.
Of course, the bgen files are not in the current directory, I just changed the log.
Anyway, the error actually occurs AFTER reading the bgen files, here is the complete log
PRSice 2.3.3 (2020-08-05)
(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)
2020-11-11 22:03:49
--cov ./braincohort_sample/cov_brainprscohort_prsice \
--extract ./braincohort_sample/wbgen.valid \
--interval 5e-05 \
--keep ./braincohort_sample/prs.brain.cohort.list \
--lower 5e-08 \
--num-auto 22 \
--out braincohort_sample/wbgen \
--pheno ./braincohort_sample/pheno_only_wbnj2 \
Initializing Genotype file:
/UKBB_GeneticData/bgen_files/ukb_imp_chr#_v3
(bgen)
With external fam file:
/UKB/sam_files/ukb_imp_chr2_v3_s222.sample
Start processing wbnojobstat.clean
==================================================
SNP extraction/exclusion list contains 5 columns, will
assume first column contains the SNP ID
Base file:
/scratch/wbnojobstat.clean.forprscs
Header of file is:
SNP A1 A2 BETA P
8103178 variant(s) observed in base file, with:
44875 variant(s) excluded based on user input
8058303 total variant(s) included from base file
Loading Genotype info from target
==================================================
487409 people (222994 male(s), 264301 female(s)) observed
15213 founder(s) included
7565465 SNPs processed in /UKBB_GeneticData/bgen_files/ukb_imp_chr1_v3.bgen
.
.
.
2565465 SNPs processed in /UKBB_GeneticData/bgen_files/ukb_imp_chr22_v3.bgen
85027610 variant(s) not found in previous data
9710 variant(s) with mismatch information
8058303 variant(s) included
Phenotype file: ./braincohort_sample/pheno_only_wbnj2
Column Name of Sample ID: FID+IID
Note: If the phenotype file does not contain a header, the
column name will be displayed as the Sample ID which is
expected.
There are a total of 1 phenotype to process