Originally posted by figo1019
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Originally posted by Mark.hz View PostTruncated BAM file may cause this problem. You need to go back to validate your BAM files by Picard.
I ran the picard tool to validate I get an error
ERROR: Read groups is empty
Rest things are OK.
Does it make a huge difference ?
regards
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Originally posted by figo1019 View PostHi Mark.hz
Have you sorted out this problem as I am also facing the similar error while running the bcf file [bcf_sync] incorrect number of fields (4 != 5) at 15:16294867.
Regards
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Originally posted by Mark.hz View PostStill have this problem when doing bcftools view for a bcf file (mpileup generated): [bcf_sync] incorrect number of fields (6 != 5) at 7:1396330564
Any help?
Have you sorted out this problem as I am also facing the similar error while running the bcf file [bcf_sync] incorrect number of fields (4 != 5) at 15:16294867.
Regards
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Still have this problem when doing bcftools view for a bcf file (mpileup generated): [bcf_sync] incorrect number of fields (6 != 5) at 7:1396330564
Any help?
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I ran into the same problem, either with or without nohup. Does anyone know how to fix? Now I am generating the raw bcf file and try to figure out what is wrong on that specific line.
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The "incorrect number of files" can happen if the file is truncated. I see it sometimes if I want to check on a big files while it's still being made by mpileup.
What's the purpose of the cat command, and the pipe?
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Same problem
I am having the same problem, which is strange as I've used this exact pipeline/command previously with no issues. Have you figured anything out?
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bcftools error
Hello,
The command
cat all.mpileup | bcftools view -bvcg - > all.var.raw.bcf
exits with the text below
[bcf_sync] incorrect number of fields (4 != 5) at 10:1696253
[afs] 0:38509.883 1:50.388 2:38.729
before exiting it outputs this text (this pattern starts at 100000)
[bcfview] 13600000 sites processed.
[afs] 0:99814.004 1:101.247 2:84.750
[bcfview] 13700000 sites processed.
[afs] 0:99786.086 1:107.189 2:106.725
all.mpileup was generated with the following command
samtools -verbose -uf reference.fasta all.bam > all.mpileup
Does anyone know what is causing this or how to fix it? I would like to be able to call both SNPs and indels with this.
Thank you
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