bac.f | R Documentation |
A dataset containing SNP frequency data for demonstration purposes. This dataset represents a small subset of SNPs with coverage and alternative allele frequency information.
bac.f
A data frame with 6 rows and 19 variables:
Chromosome or reference identifier (character).
Position of the SNP on the chromosome (integer).
Unused identifier; typically NA (character).
Reference nucleotide (character).
Alternative nucleotide(s), separated by commas (character).
Quality score of the SNP (character).
Filter status; typically NA (character).
Additional information about the SNP, such as coverage and allele counts (character).
Genotype of the SNP (character).
Phred-scaled likelihoods for genotypes (character).
Total coverage at the SNP position (character).
Per-sample depth for each allele, separated by commas (character).
Genotype quality (character).
Isolate identifier (character).
Total coverage at the SNP position (numeric).
Coverage of the reference nucleotide (numeric).
Coverage of the first alternative nucleotide (numeric).
Relative frequency of the reference nucleotide (numeric).
Relative frequency of the first alternative nucleotide (numeric).
data(bac.f)
head(bac.f)
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