Closed JAYRJPT closed 1 year ago
Hey Jay, I've solved this issue by renaming the chromosomes via 'bcftools annotate --rename-chrs RenameTable.txt old.vcf > new.vcf'. The table for renaming the chromosomes only consists of two space-separated columns with the 'old' names and the new names (without header). chr1 1 chr2 2 etc ...
Hope it helps, Mathias
Hey Jay, I've solved this issue by renaming the chromosomes via 'bcftools annotate --rename-chrs RenameTable.txt old.vcf > new.vcf'. The table for renaming the chromosomes only consists of two space-separated columns with the 'old' names and the new names (without header). chr1 1 chr2 2 etc ...
Hope it helps, Mathias
Hi Mathias, Thanks for your suggestion. My issue is resolved. I have removed the first line of the vcf file in which AD information was not available.
Hello Jan, I have generated the VCF files using GATK pipeline for RNAseqCNV analysis. However, one of my vcf file showing error in RNAseqCNV tool. Here is my command and error.
> RNAseqCNV_wrapper(config = "/media/deepak/jay_doc/MERCILENA/RNASEQCNV_F_G_H/RNASEQCNV/config_file", metadata = "/media/deepak/jay_doc/MERCILENA/RNASEQCNV_F_G_H/RNASEQCNV/snv_metadata.csv", snv_format = "vcf", batch = FALSE, genome_version = "hg38")
[1] "Analysis initiated" [1] "Normalization for sample: F9 completed" [1] "Preparing file with snv information for: F9" Reading in vcf file.. Incorrect vcf file format. No allele depth (AD) in FORMAT columnI have checked the file and it look similar with the other which ran without any error in the tool. Kindly look at the vcf file
Thanks and Regards, Jay