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