assess_missing_data_pca |
Vizualise how missing data thresholds affect sample clustering |
assess_missing_data_tsne |
Vizualise how missing data thresholds affect sample clustering |
distance_thin |
Filter a vcf file based on distance between SNPs on a given scaffold |
filter_allele_balance |
Filter out heterozygous genotypes failing an allele balance check |
filter_biallelic |
Remove SNPs with more than two alleles |
hard_filter |
Hard filter a vcf file by depth and genotype quality (gq) |
max_depth |
Vizualise and filter based on mean depth across all called SNPs |
min_mac |
Vizualise, filter based on Minor Allele Count (MAC) |
missing_by_sample |
Vizualise missing data per sample, remove samples above a missing data cutoff |
missing_by_snp |
Vizualise missing data per SNP, remove SNPs above a missing data cutoff |
popmap |
Popmap for example scrub-jay vcfR file |
SNPfiltR |
SNPfiltR: A package for interactively visualizing and filtering SNP datasets |
vcfR.example |
Example scrub-jay vcfR file |