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bcftools mpileup create an empty output file

I try to run bcftools to create a vcf file of my data, but I keep getting empty output files

The command I use are 

bwa mem -t14 -M ~/genomes/Sce.R64-1-1/bwaIndex/Sce.R64-1-1 HHgDNA1.R1.fastq.gz HHgDNA1.R2.fastq.gz | samtools view -buh - | samtools sort -@ 14 -o bamFiles/bwa/HHgDNA1.sorted.bam
samtools index bamFiles/bwa/HHgDNA1.sorted.bam
bcftools mpileup -A  -t 10 -Ou -f $REF_FASTA bamFiles/bwa/HHgDNA1.sorted.bam

while $REF_FASTA is the fastA file also used to create the bwa indexed genome. I know the output goes to STDOUT, but I'm still trying to figure it out. looking at the bam files i have ~99% mapped and properly paired reads.

All I get is the header of the file, but nothing more.

any ideas what is going on?

thanks

bcftools mpileup samtools bwa bam
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written by Assa Yeroslaviz Assa Yeroslaviz

I think I do. I have removed it after I got nothing from the bcftools call command to see why the output file is empty. This is also, why I output it to the STDOUT, but all I get is the header. From what I remember from the samtools mpileup one can also get an output file from calling only the mpileup. But here I get nothing.

• 0 views • link
written by Assa Yeroslaviz Assa Yeroslaviz

So, it functions correctly but just calls nothing / no variants. Are your contigs named correctly?, e.g., 'chr1' versus '1'? Check, also, the header that's produced, as it should record commands that were used during processing - check for anything unusual.

Is $REF_FASTA being expanded correctly in your shell?

• 0 views • link
written by Kevin Blighe Kevin Blighe

Are your contigs named correctly?, e.g., 'chr1' versus '1'? yes as far as I can tell

the header of my bam file

samtools view -H bamFiles/bwa/HHgDNaaA1.sorted.bam 
@HD     VN:1.5  SO:coordinate
@SQ     SN:I    LN:230218
@SQ     SN:II   LN:813184
@SQ     SN:III  LN:316620
@SQ     SN:IV   LN:1531933
@SQ     SN:V    LN:576874
@SQ     SN:VI   LN:270161
@SQ     SN:VII  LN:1090940
@SQ     SN:VIII LN:562643
@SQ     SN:IX   LN:439888
@SQ     SN:X    LN:745751
@SQ     SN:XI   LN:666816
@SQ     SN:XII  LN:1078177
@SQ     SN:XIII LN:924431
@SQ     SN:XIV  LN:784333
@SQ     SN:XV   LN:1091291
@SQ     SN:XVI  LN:948066
@SQ     SN:Mito LN:85779
@PG     ID:bwa  PN:bwa  VN:0.7.17-r1188 CL:bwa mem -t14 -M bwaIndex/Sce data/HHgDNA1.conc.R1.fastq.gz data/HHgDNA1.conc.R2.fastq.gz

the fastA file contains the chromosomes 

$ grep ">" Sce.R64-1-1.fa
>I dna:chromosome chromosome:R64-1-1:I:1:230218:1 REF
>II dna:chromosome chromosome:R64-1-1:II:1:813184:1 REF
>III dna:chromosome chromosome:R64-1-1:III:1:316620:1 REF
>IV dna:chromosome chromosome:R64-1-1:IV:1:1531933:1 REF
>V dna:chromosome chromosome:R64-1-1:V:1:576874:1 REF
>VI dna:chromosome chromosome:R64-1-1:VI:1:270161:1 REF
>VII dna:chromosome chromosome:R64-1-1:VII:1:1090940:1 REF
>VIII dna:chromosome chromosome:R64-1-1:VIII:1:562643:1 REF
>IX dna:chromosome chromosome:R64-1-1:IX:1:439888:1 REF
>X dna:chromosome chromosome:R64-1-1:X:1:745751:1 REF
>XI dna:chromosome chromosome:R64-1-1:XI:1:666816:1 REF
>XII dna:chromosome chromosome:R64-1-1:XII:1:1078177:1 REF
>XIII dna:chromosome chromosome:R64-1-1:XIII:1:924431:1 REF
>XIV dna:chromosome chromosome:R64-1-1:XIV:1:784333:1 REF
>XV dna:chromosome chromosome:R64-1-1:XV:1:1091291:1 REF
>XVI dna:chromosome chromosome:R64-1-1:XVI:1:948066:1 REF
>Mito dna:chromosome chromosome:R64-1-1:Mito:1:85779:1 REF

Check, also, the header that's produced, as it should record commands that were used during processing - check for anything unusual.

This is the output I get from the bcftools mpielup call 

bcftools mpileup -A -t 10 -Ou -f /home/yeroslaviz/poolFolders/pool-bcfngs/genomes/Sce.R64-1-1.fa bamFiles/bwa/HHgDNaaA1.sorted.bam 
[mpileup] 1 samples in 1 input files
BCFa
##fileformat=VCFv4.2
##FILTER=<ID=PASS,Description="All filters passed",IDX=0>
##bcftoolsVersion=1.8+htslib-1.8
##bcftoolsCommand=mpileup -A -t 10 -Ou -f /home/yeroslaviz/poolFolders/pool-bcfngs/genomes/Sce.R64-1-1.fa bamFiles/bwa/HHgDNaaA1.sorted.bam
##reference=file:///home/yeroslaviz/poolFolders/pool-bcfngs/genomes/Sce.R64-1-1.fa
##contig=<ID=I,length=230218,IDX=0>
##contig=<ID=II,length=813184,IDX=1>
##contig=<ID=III,length=316620,IDX=2>
##contig=<ID=IV,length=1531933,IDX=3>
##contig=<ID=V,length=576874,IDX=4>
##contig=<ID=VI,length=270161,IDX=5>
##contig=<ID=VII,length=1090940,IDX=6>
##contig=<ID=VIII,length=562643,IDX=7>
##contig=<ID=IX,length=439888,IDX=8>
##contig=<ID=X,length=745751,IDX=9>
##contig=<ID=XI,length=666816,IDX=10>
##contig=<ID=XII,length=1078177,IDX=11>
##contig=<ID=XIII,length=924431,IDX=12>
##contig=<ID=XIV,length=784333,IDX=13>
##contig=<ID=XV,length=1091291,IDX=14>
##contig=<ID=XVI,length=948066,IDX=15>
##contig=<ID=Mito,length=85779,IDX=16>
##ALT=<ID=*,Description="Represents allele(s) other than observed.">
##INFO=<ID=INDEL,Number=0,Type=Flag,Description="Indicates that the variant is an INDEL.",IDX=1>
...
#CHROM  POS     ID      REF     ALT     QUAL    FILTER  INFO    FORMAT  bamFiles/bwa/HHgDNaaA1.sorted.bam

I can't see anything out of the ordinary.

Is $REF_FASTA being expanded correctly in your shell?

yes, but I have tried it with both the full path and the variable with no differences in the results

• 0 views • link
written by Assa Yeroslaviz Assa Yeroslaviz

1 answer

ok, the problem was using the wrong threads parameter. Somehow I assumed that the threads number can be called with -t. But unfortunately this is a region parameter, and as such for a chromosome I don't have in my data set (as I have I,II,III, etc)

so calling it correctly would be 

bcftools mpileup -A --threads 10 -Ou -f $REF_FASTA bamFiles/bwa/HHgDNA1.sorted.bam
• 0 views • link
written by Assa Yeroslaviz Assa Yeroslaviz

Thanks for posting the answer. -t may have been used for threads in previous versions of bcftools or samtools - not sure.

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written by Kevin Blighe Kevin Blighe

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