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, 17:09, 18 July 2018
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| == About bafRegress == | | == About bafRegress == |
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− | '''bafRegress''' is actually a pair of scripts, one python and one R. The python script is the main interface and handles the parsing of Illumina final report files. The R script actually performs the regression model and provides the contamination estimates. | + | '''bafRegress''' is actually a pair of scripts, one Python (2.7) and one R. The Python script is the main interface and handles the parsing of Illumina final report files. The R script actually performs the regression model and provides the contamination estimates. |
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| To use this program, you will need Final Report files from BeadStudio/GenomeStudio. You will need to have columns for the genotypes using the A/B Illumina coded alleles as well as the Illumina reported B allele frequency in addition to the standard sample/marker columns. | | To use this program, you will need Final Report files from BeadStudio/GenomeStudio. You will need to have columns for the genotypes using the A/B Illumina coded alleles as well as the Illumina reported B allele frequency in addition to the standard sample/marker columns. |