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Related documents:
| Haplotype Frequency Sort Order |
| Haplotype | All | Controls | Cases |
AGCC | 539 | 26.6% | 288 | 27.9% | 251 | 25.3% |
ACGT | 479 | 23.6% | 320 | 31.0% | 159 | 16.0% |
AGGT | 444 | 21.9% | 155 | 15.0% | 289 | 29.1% |
TGGT | 426 | 21.0% | 209 | 20.3% | 217 | 21.8% |
AGGC | 134 | 6.6% | 58 | 5.6% | 76 | 7.6% |
AGCT | 04 | 0.2% | 02 | 0.2% | 02 | 0.2% |
Totals | 2026 | | 1032 | | 994 | |
| Haplotype Alphabetic Sort Order |
| Haplotype | All | Controls | Cases |
ACGT | 479 | 23.6% | 320 | 31.0% | 159 | 16.0% |
AGCC | 539 | 26.6% | 288 | 27.9% | 251 | 25.3% |
AGCT | 04 | 0.2% | 02 | 0.2% | 02 | 0.2% |
AGGC | 134 | 6.6% | 58 | 5.6% | 76 | 7.6% |
AGGT | 444 | 21.9% | 155 | 15.0% | 289 | 29.1% |
TGGT | 426 | 21.0% | 209 | 20.3% | 217 | 21.8% |
Totals | 2026 | | 1032 | | 994 | |
Minimal SNP (highlighted columns) needed to unambiguously distinguish haplotypes seen more than once, by population group Please note that this an experimental resource which is still under test.Please email Ross Lazarus if you have comments or find any errors or anomalies
Minimal sets of haplotype tagging SNP for CCL2 in Cases
| 2 |
4 |
4 |
5 |
|
| 9 |
1 |
7 |
9 |
# |
| 3 |
4 |
1 |
7 |
|
| 4 |
4 |
0 |
2 |
|
| A |
G |
G |
T |
(289) |
| A |
G |
C |
C |
(251) |
| T |
G |
G |
T |
(217) |
| A |
C |
G |
T |
(159) |
| A |
G |
G |
C |
(76) |
| A |
G |
C |
T |
(2) |
Legend: - Same allele as first row of the corresponding SNP column
- Variant allele:
Minimal sets of haplotype tagging SNP for CCL2 in Controls
| 2 |
4 |
4 |
5 |
|
| 9 |
1 |
7 |
9 |
# |
| 3 |
4 |
1 |
7 |
|
| 4 |
4 |
0 |
2 |
|
| A |
C |
G |
T |
(320) |
| A |
G |
C |
C |
(288) |
| T |
G |
G |
T |
(209) |
| A |
G |
G |
T |
(155) |
| A |
G |
G |
C |
(58) |
| A |
G |
C |
T |
(2) |
Legend: - Same allele as first row of the corresponding SNP column
- Variant allele:
The haplotypes shown above are comprised of alleles at the following SNP locations in the order show. The first column is the allele position in the haplotype. The SNP column is the SNP position in the reference sequence (1=first base). The RelativeOffset column is the SNP offset relative to the ATG start codon. | # | SNP | RelativeOffset |
| 1 | 2934 | -2138 |
| 2 | 4144 | -928 |
| 3 | 4710 | -362 |
| 4 | 5972 | 900 |
* The PHASE software package was used to generate the contents of this output file.
Custom written Python scripts (available on request) were used to create the input files for
PHASE (from the raw data files in SeattleSNPs "prettybase" format available
elsewhere on this site) and also to process the PHASE output into more useful formats.
PHASE uses MCMC methods and is available from http://www.stats.ox.ac.uk/mathgen/software.html .
The results were obtained by running PHASE independently for each of the separate
groups shown and amalgamating the results.
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