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  • oliviajm
    replied
    Originally posted by mark.dunning View Post
    Can I ask if the vcf provided by varscan is valid though? I have used the latest version and tried to annotate with annovar (via their conversion perl script) but I get an error.

    NOTICE: for SNPs, column 6 and beyond MAY BE heterozygosity status, quality score, read depth, RMS mapping quality, quality by depth, if these information can be recognized automatically
    NOTICE: for indels, column 6 and beyond MAY BE heterozygosity status, quality score, read depth, read count supporting indel call, RMS mapping quality, if these information can be recognized automatically

    Similarly, using vcf-stats from vcftools also gives an error;

    Different number of columns at chr1:12198 (expected 10, got 9)
    Error not recoverable, exiting.


    Here is the head of my varscan vcf file

    ##fileformat=VCFv4.0
    ##source=VarScan2
    ##INFO=<ID=DP,Number=1,Type=Integer,Description="Total Depth">
    ##FILTER=<ID=str10,Description="Less than 10% or more than 90% of variant supporting reads on one strand">
    ##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
    ##FORMAT=<ID=GQ,Number=1,Type=Integer,Description="Genotype Quality">
    ##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Read Depth">
    #CHROM POS ID REF ALT QUAL FILTER INFO FORMAT Sample1
    chr1 12198 G C . PASS DP=107 GT:GQP 1/1:35:107
    chr1 12266 G A . PASS DP=53 GT:GQP 0/1:4:53


    Regards,

    Mark
    Hi Mark,

    I got a similar problem with another software when I tried to provide it with a vcf file coming from VarScan mpileup2indel. It seems that in the vcf files obtained with VarScan the QUAL column is empty. So when the file is open by another tool, the number of column is wrong and the data in the columns don't match with the name of the column. ("PASS" should be in the "FILTER" column, and here it seems to be in the "QUAL" column.)
    So you need to add a column filled with a dot under the "QUAL" name.
    In my case, I used the command :
    awk '{ if ($1 ~ "^#") { print $0} else { sub("",".\t",$6); print $1"\t"$2"\t"$3"\t"$4"\t"$5"\t"$6"\t"$7"\t"$8"\t"$9"\t"$10"\t"$11"\t"$12} }' VarScanfile.vcf > outputFile.vcf
    and it solved the problem.

    Hope it will help you.

    Olivia

    EDIT : just found this : http://seqanswers.com/forums/showthread.php?t=20000
    Last edited by oliviajm; 06-08-2012, 12:00 AM.

    Leave a comment:


  • fjrossello
    replied
    Originally posted by dkrtndhkd View Post
    what about somatic option??

    I couldn't find the vcf file output option command...
    Hi dkrtndhkd,

    You can also set --output-vcf to 1 for somatic.

    Cheers,

    Fernando

    Leave a comment:


  • dkrtndhkd
    replied
    what about somatic option??

    I couldn't find the vcf file output option command...

    Leave a comment:


  • mark.dunning
    replied
    Can I ask if the vcf provided by varscan is valid though? I have used the latest version and tried to annotate with annovar (via their conversion perl script) but I get an error.

    NOTICE: for SNPs, column 6 and beyond MAY BE heterozygosity status, quality score, read depth, RMS mapping quality, quality by depth, if these information can be recognized automatically
    NOTICE: for indels, column 6 and beyond MAY BE heterozygosity status, quality score, read depth, read count supporting indel call, RMS mapping quality, if these information can be recognized automatically

    Similarly, using vcf-stats from vcftools also gives an error;

    Different number of columns at chr1:12198 (expected 10, got 9)
    Error not recoverable, exiting.


    Here is the head of my varscan vcf file

    ##fileformat=VCFv4.0
    ##source=VarScan2
    ##INFO=<ID=DP,Number=1,Type=Integer,Description="Total Depth">
    ##FILTER=<ID=str10,Description="Less than 10% or more than 90% of variant supporting reads on one strand">
    ##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
    ##FORMAT=<ID=GQ,Number=1,Type=Integer,Description="Genotype Quality">
    ##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Read Depth">
    #CHROM POS ID REF ALT QUAL FILTER INFO FORMAT Sample1
    chr1 12198 G C . PASS DP=107 GT:GQP 1/1:35:107
    chr1 12266 G A . PASS DP=53 GT:GQP 0/1:4:53


    Regards,

    Mark

    Leave a comment:


  • dkoboldt
    replied
    Hello,

    The latest version of VarScan (v2.2.11, just posted) includes a VCF output option for somatic mutations.

    This option was already available for multi-sample germline variant calling (mpileup2snp, mpileup2cns, mpileup2indel commands).

    Just set --output-vcf to 1.

    Yours,

    Dan Koboldt

    Leave a comment:


  • dkrtndhkd
    started a topic varscan-annotation pipeline?

    varscan-annotation pipeline?

    How to connect VarScan output and annotation tools?

    is there any useful tool to directly annotate the varscan's output file?

    or I have to change the form of the output file to vcf format?

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