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consider adding filters for sequencing quality (Phred score): with vcftools, the option --minQ can be used
explore filtering for individual genotype coverage (not average coverage across all samples): this may be done in vcftools with the option --minDP (DP FORMAT tag must be specified for all sites)
vcftools, the option--minQcan be usedvcftoolswith the option--minDP(DP FORMAT tag must be specified for all sites)