A dataset containing real genotype likelihoods in phred scores for 1,000 SNPs. The data is available for ten individuals and the first 1,000 SNPs on chromosome 1. The data corresponds to a low-fold sequencing experiment. There are three columns per individuals (for genotypes 00, 01 and 11).
BBB_NMP_pl_subset
A data frame with 1,000 rows and 35 variables:
The chromosome number
The marker id
The position of the marker
The name of the first marker allele
The name of the second marker allele
The AA phred likelihood for the first individual
The AB phred likelihood for the first individual
The BB phred likelihood for the first individual
The AA phred likelihood for the second individual
The AB phred likelihood for the second individual
The BB phred likelihood for the second individual
The phred likelihoods for the other individuals