Dear all,
I am really a newbie in NGS analysis, so I am really sorry if I am wrong.
I have 4 vcf files and I would like to merge them.
The problem is that 3 of them contain not only the variants but every position from ~60k to ~130M bp (http://cdna.eva.mpg.de/denisova/VCF/human/) and 1 files in bam format. What I have done is to call the variants with mpileup and created the vcf files from the unique bam file that i had.
Which is in your opinioon the best way to merge all this 4 files? vcf-merge in vcftools could be an option but create a huge files, what i would like to have is a vcf file with the mutations for my 4 samples.
In addition I would like to add ID information fpr each SNP, is it vcf annotate a good option?
Thank you very much in advanc for four help.
Have a nice day
Francesco
I am really a newbie in NGS analysis, so I am really sorry if I am wrong.
I have 4 vcf files and I would like to merge them.
The problem is that 3 of them contain not only the variants but every position from ~60k to ~130M bp (http://cdna.eva.mpg.de/denisova/VCF/human/) and 1 files in bam format. What I have done is to call the variants with mpileup and created the vcf files from the unique bam file that i had.
Which is in your opinioon the best way to merge all this 4 files? vcf-merge in vcftools could be an option but create a huge files, what i would like to have is a vcf file with the mutations for my 4 samples.
In addition I would like to add ID information fpr each SNP, is it vcf annotate a good option?
Thank you very much in advanc for four help.
Have a nice day
Francesco
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