Problem merging plink files for somatic variants.
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8 months ago
Palgrave ▴ 130

I have 5000 somatic vcf files converted to plink format that I try to merge using this command

plink --bfile file1 --merge-list files.bed.txt --make-bed --out Merged.Plink

However, the output looks strange and I get several errors (1107578 to be exact) like below: Any ideas?

...
Warning: Multiple chromosomes seen for variant 'gridss335fb_1314h'.
Warning: Multiple chromosomes seen for variant 'unbalanced_22'.
Warning: Multiple chromosomes seen for variant 'gridss1070bb_15h'.
Warning: Multiple chromosomes seen for variant 'gridss584ff_92h'.
Error: 797428 variants with 3+ alleles present.
* If you believe this is due to strand inconsistency, try --flip with
  Merged.Plink-merge.missnp.
  (Warning: if this seems to work, strand errors involving SNPs with A/T or C/G
  alleles probably remain in your data.  If LD between nearby SNPs is high,
  --flip-scan should detect them.)
* If you are dealing with genuine multiallelic variants, we recommend exporting
  that subset of the data to VCF (via e.g. '--recode vcf'), merging with
  another tool/script, and then importing the result; PLINK is not yet suited
  to handling them.
See https://www.cog-genomics.org/plink/1.9/data#merge3 for more discussion.

End time: Sat Mar  9 08:19:15 2024

The output:

head Merged.Plink-merge.fam
ACTN01020001R   ACTN01020001R   0   0   0   -9
ACTN01020001T   ACTN01020001T   0   0   0   -9
ACTN01020002R   ACTN01020002R   0   0   0   -9
ACTN01020002T   ACTN01020002T   0   0   0   -9
ACTN01020003R   ACTN01020003R   0   0   0   -9
ACTN01020003T   ACTN01020003T   0   0   0   -9
ACTN01020005R   ACTN01020005R   0   0   0   -9
ACTN01020005T   ACTN01020005T   0   0   0   -9
ACTN01020006R   ACTN01020006R   0   0   0   -9
ACTN01020006T   ACTN01020006T   0   0   0   -9


 wc Merged.Plink-merge.missnp
  797428   797428 12522503 Merged.Plink-merge.missnp
plink somatic vcf • 583 views
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Sorry, finxed now.

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