Hi all
I'm using galaxy and I need to know allele frequency (MAF, minor frequency allele) for each SNP or variant.
I click on "view data" but it show as frequency's value (AF=) only 1,00 or 0,50
I wonder where I'm going wrong..
Hi all
I'm using galaxy and I need to know allele frequency (MAF, minor frequency allele) for each SNP or variant.
I click on "view data" but it show as frequency's value (AF=) only 1,00 or 0,50
I wonder where I'm going wrong..
Hello,
Please see the tool "NGS: VCF Manipulation -> VCFfixup" on the public Main Galaxy instance. It is also available in the tool shed for use in a local/cloud.
Best, Jen, Galaxy team
Hello, thank you for answer.
I used "NGS: VCF Manipulation -> VCFfixup" but problem persists.
Any other suggest?
thank you in advance.
I have try to use some tools as Variant annotator or MAF exploit but it shows me these errors
Fatal error: Exit code 1 () Error: Input file does not seem to have a proper header line. Adding an artificial header..Traceback (most recent call last): File "/galaxy/main/shed_tools/toolshed.g2.bx.psu.edu/repos/boris/hetbox/8d2c4c11fd8f/hetbox/hetbox Fatal error: Exit code 1 () Error in input VCF: Incorrect variant data format (must contain a single '='). Failed on line: chrM 72 . T C 123.03 LowCoverage ABHom=1.00;AC=2;AF=1.00;AN=2;DP=4;Dels=0.00;FS=0.000;HaplotypeScore=0.0000;MLEAC=2;MLEAF=1.00;MQ=4
Is there a problem with VCF file?