NOTICE: This software is available for use free of charge for academic research use only. Commercial users, for profit companies or consultants, and non-profit institutions not qualifying as "academic research" must contact the Stanford Office of Technology Licensing for a separate license to use RFMIX. This applies to this repository directly and any other repository that includes RFMIX source, executables, or git commands that pull/clone this repository as part of its function. Such repositories, whether mine or others, must include this notice. Academic users may fork this repository and modify and improve RFMIX to suit their research needs, but also inherit these terms and must include a licensing notice to that effect.
The forward-backward result output is a tab separated file with the name <output basename>.fb.tsv
The first line is a comment line, that specifies the order of subpopulations: eg:
#reference_panel_population: golden_retriever labrador_retriever poodle poodle_small
The second line specifies the column names, and every following lines gives data on a chunk of the genome, called a conditional random field (CRF) point.
The first four columns specify the chromosome, genetic marker's physical position in basepair units and genetic position in centiMorgans, and the genetic marker's numerical index in the rfmix genetic map input file. The remaining columns give the probabilities that the CRF point for a genotype's haplotype was assigned to a specific reference panel population. A genotype has two haplotypes, so the number of probabilities for a genotype is 2*(number of reference panel populations). The number of columns in the file is 4 + (number of genotypes) * 2 * (number of reference panel populations.