Dear All,
Our maize inbreed line collection have been genotyped with maize DArTseq (1.0) by the Diversity Arrays Technology Ltd.
I have already used TASSEL to analyse presence-absence data many times, but I would like to  to analyse SNP data this time,
I have read the online manual but I am not sure how  input the data in the hapmap file to perform GWAS.
 SNP 1 Row Mapping Format coding is the following: "0" = Reference allele homozygote, "1" = SNP allele homozygote,
 "2"= heterozygote and "-" = double null/null allele homozygote (absence of fragment with SNP in genomic representation)
The dataset looks like this:
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
  | AlleleID | AlleleSequence | TrimmedSequence | Chrom_Maize_v8 | ChromPos_Maize_v8 | AlnCnt_Maize_v8 | AlnEvalue_Maize_v8 | Chrom_Maize_v329 | ChromPos_Maize_v329 | AlnCnt_Maize_v329 | AlnEvalue_Maize_v329 | SNP | SnpPosition | CallRate | OneRatioRef | OneRatioSnp | FreqHomRef | FreqHomSnp | FreqHets | PICRef | PICSnp | AvgPIC | AvgCountRef | AvgCountSnp | RepAvg | genotype1 | Genotype 20 | 
 
  | 4585424|F|0-20:A>C-20:A>C | TGCAGGCACCTGAGCGGCTCATACCATGGCTTGTGCGACACCTCCTACACCCCCTGCCTAGATACATGA | TGCAGGCACCTGAGCGGCTCATACCATGGCTTGTGCGACACCTCCTACACCCCCTGCCTAGATACATGA | 5 chromosome:AGPv2:5:1:217872852:1 chromosome 5 | 66000337 | 1 | 3.01E-26 | 5 dna:chromosome | 66029138 | 1 | 3.01E-26 | 20:A>C | 20 | 1 | 0.502703 | 0.502703 | 0.497297 | 0.497297 | 0.005405 | 0.499985 | 0.499985 | 0.499985 | 53.46491 | 49.24786 | 1 | 0 | 0 | 
 
  | 24026074|F|0-11:G>A-11:G>A | TGCAGAAAGGAGTATGGCCAAAACTTTAAACATGAGATCGGAAGAGCGGTTCAGCAGGAATGCCGAGAC | TGCAGAAAGGAGTATGGCCAAAACTTTAAACATG | 2 chromosome:AGPv2:2:1:237068873:1 chromosome 2 | 212362874 | 1 | 1.20E-09 | 2 dna:chromosome | 213027563 | 1 | 1.20E-09 | 11:G>A | 11 | 1 | 0.502703 | 0.497297 | 0.502703 | 0.497297 | 0 | 0.499985 | 0.499985 | 0.499985 | 58.9375 | 61.84746 | 1 | 1 | 1 | 
 
  | 4582318|F|0-51:T>C-51:T>C | TGCAGGTATTCCCTTGAGGAGCAGGCGCTCGCCGAGCAACTTTCCAATCTTTGCAGCTGCTGCGACGTC | TGCAGGTATTCCCTTGAGGAGCAGGCGCTCGCCGAGCAACTTTCCAATCTTTGCAGCTGCTGCGACGTC | 2 chromosome:AGPv2:2:1:237068873:1 chromosome 2 | 107189279 | 1 | 1.80E-28 | 2 dna:chromosome | 107819360 | 1 | 1.80E-28 | 51:T>C | 51 | 1 | 0.508108 | 0.497297 | 0.502703 | 0.491892 | 0.005405 | 0.499869 | 0.499985 | 0.499927 | 27.05882 | 29.04464 | 1 | 0 | 0 | 
I can find the "chromosome" and the "position". I also know what is the SNP, e.g.
But I do not know how to code it according to "Nucleotide Codes (Derived from IUPAC)"
for example how to code a heterozygote?
Can someone tell me how to do that or send some example.
Thank you for your help!
István