Thanks, that helps a lot!
I know there's another question along the same lines, but I suspect my situation is slightly different...
I have an Illumina Final Report file, but I don't have access to Illumina directly, so I have to work with the file I have or I have to request one with more columns from someone else. My Final Report files have these columns:
SNP Name Sample ID Allele1 - Top Allele2 - Top GC Score Sample Name Sample Group Sample Index SNP Index SNP Aux Allele1 - Forward Allele2 - Forward Allele1 - Design Allele2 - Design Allele1 - AB Allele2 - AB Allele1 - Plus Allele2 - Plus Chr Position GT Score Cluster Sep SNP ILMN Strand Customer Strand Top Genomic Sequence Plus/Minus Strand Theta R X Y X Raw Y Raw B Allele Freq Log R Ratio CNV Value CNV Confidence
From reading other questions, I believe I need to produce three files: a .lgen, a .map, and a .fam. My main question is this, I suppose: which columns do I use to produce each file?
Thanks!
1 answer
##Map file:
Column 1 - Chr: Chr
Column 2 - SNP: SNP Name
Column 3 - Genetic distance: 0
Column 4 - Base-pair position: Position
##Lgen file:
Column 1 - Family ID: Sample Group
Column 2 - Individual ID: Sample ID
Column 3 - SNP: SNP Name
Column 4 - A1: Allele1 - Forward
Column 5 - A2: Allele2 - Forward
##Fam file:
Column 1 - Family ID: Sample Group
Column 2 - Individual ID: Sample ID
Column 3 - Paternal ID: 0
Column 4 - Maternal ID: 0
Column 5 - Sex: 0
Column 6 - Phenotype: 0
You should add sex and age to your fam file afterward. If you have some family, add Paternal and Maternal ID too.
I think you should be able to use these files with PLINK, but I can't be sure because I don't have any example.
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