Hi all,
I'm relatively new to analyzing sequence data, and have a question about using samtools for SNP calling from exome data. When going from a bcf file to a vcf file, is there a way to set a limit that it will only make the SNP calls at base positions that have a minimum read depth. For example, if I only want SNPs to be called when a base has a read depth of 10x or greater, is there a specific flag for this, or would this be done by filtering through the vcf file afterwards? The samtools documentation is not completely clear to me.
Thanks for your help...
I'm relatively new to analyzing sequence data, and have a question about using samtools for SNP calling from exome data. When going from a bcf file to a vcf file, is there a way to set a limit that it will only make the SNP calls at base positions that have a minimum read depth. For example, if I only want SNPs to be called when a base has a read depth of 10x or greater, is there a specific flag for this, or would this be done by filtering through the vcf file afterwards? The samtools documentation is not completely clear to me.
Thanks for your help...
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