TABLE I.
Haplotype | S1: R2 = 0.41, MAF = 0.39 |
S2: R2 = 0.59, MAF = 0.28 |
S3: R2 = 0.70, MAF = 0.15 |
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UTTTT | Frequency | TTTUT | Frequency | TTUTT | Frequency | |
h1 | 00011 | 0.0513 | 00100 | 0.3171 | 00000 | 0.0513 |
h2 | 00100 | 0.0260 | 00101 | 0.0988 | 00100 | 0.1460 |
h3 | 01011 | 0.0855 | 00111 | 0.2027 | 01000 | 0.6958 |
h4 | 01100 | 0.3094 | 01001 | 0.1518 | 10011 | 0.1069 |
h5 | 01101 | 0.1377 | 10100 | 0.1059 | ||
h6 | 11011 | 0.0085 | 10101 | 0.0209 | ||
h7 | 11100 | 0.1775 | 10111 | 0.0793 | ||
h8 | 11101 | 0.0247 | 11001 | 0.0235 | ||
h9 | 11111 | 0.1794 | ||||
Haplotype | S4: R2 = 0.81, MAF = 0.33 |
S5: R2 = 0.84, MAF = 0.24 |
S6: R2 = 0.93, MAF = 0.15 |
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UTTTT | Frequency | TTUTT | Frequency | TTUTT | Frequency | |
h1 | 00011 | 0.2846 | 01101 | 0.2852 | 00011 | 0.0513 |
h2 | 00101 | 0.0128 | 10100 | 0.2510 | 00100 | 0.0260 |
h3 | 00111 | 0.0342 | 11000 | 0.2393 | 01011 | 0.0855 |
h4 | 10101 | 0.2374 | 11100 | 0.0321 | 01100 | 0.3094 |
h5 | 10111 | 0.1917 | 11101 | 0.0963 | 01101 | 0.1377 |
h6 | 11110 | 0.2393 | 11110 | 0.0961 | 11011 | 0.0085 |
h7 | 11100 | 0.1775 | ||||
h8 | 11101 | 0.0247 | ||||
h9 | 11111 | 0.1794 | ||||
Haplotype | S7: R2 = 0.95, MAF = 0.09 |
S8: R2 = 0.98, MAF = 0.28 |
S9: R2 = 0.98, MAF = 0.29 |
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UTTTT | Frequency | TTUTT | Frequency | TTTTU | Frequency | |
h1 | 00111 | 0.3809 | 01000 | 0.4231 | 01000 | 0.4231 |
h2 | 01110 | 0.2350 | 01010 | 0.1154 | 01010 | 0.1154 |
h3 | 01111 | 0.2900 | 01011 | 0.0043 | 01011 | 0.0043 |
h4 | 11001 | 0.0897 | 01111 | 0.2821 | 01111 | 0.2821 |
h5 | 11111 | 0.0044 | 10010 | 0.1751 | 10010 | 0.1751 |
“U” and “T” indicate the untyped and typed SNP positions, respectively. R2 is the squared correlation between the expected and true allele counts [Stram, 2004]. MAF is the minor allele frequency of the untyped SNP.