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Routines for reading and manipulating GWAS data in .bed files
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Data from Genome-wide association studies
are often saved as a PLINK binary biallelic genotype table
or .bed file.
To be useful, such files should be accompanied by a .fam file, containing metadata on the rows of the table, and a .bim file,
containing metadata on the columns.
The .fam and .bim files are in tab-separated format.
A SNP corresponds to a nucleotide position on the genome where some degree of variation has been observed in a population,
with each individual have one of two possible alleles at that position on each of a pair of chromosomes.
Three possible types can be observed are:
homozygous allele 1, coded as 0x00, heterzygous, coded as 0x10, and homozygous allele 2, coded as 0x11.
Missing values are coded as 0x01.
A single column - one SNP position over all m individuals - is packed into an
array of div(m + 3, 4) bytes (UInt8 values).
The package has not yet been registered and must be installed using the repository location.
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