User:David Ewing Duncan
| Public Genomes | |
|---|---|
| Summary | Full genome from Complete Genomics, but also microarrays from 23andMe, Navigenics, and deCODEme |
| Promethease | report |
|---|---|
| Summary | pooled |
| Platform |
| Promethease | report |
|---|---|
| Summary | Full genome sequence |
| Platform | Complete Genomics |
| Promethease | report |
|---|---|
| Summary | |
| Platform | 23andMe v2 |
| Promethease | report |
|---|---|
| Summary | |
| Platform | deCODEme |
| Promethease | report |
|---|---|
| Summary | |
| Platform | Navigenics |
David Ewing Duncan is the author of Experimental Man: What one man’s body reveals about his future, your health, and our toxic world. He's written about SNPedia for an MIT Technology Review article. He's also Personal Genome Project participant 13. His pooled and various platform specific reports are updated regularly.
In June 2011, User:David Ewing Duncan as part of the Personal Genome Project received data back from Complete Genomics masterVarBeta format. This does not report his 'normals' enabling a report with 5243 genotypes. Contrast that to the 11627 possible on his pooled microarrays or the 16k found in User:NA06985 or User:NA18504 which included Complete Genomics dbSNP files. By July the dbSNPAnnotated file provided 19,379 genotypes for the 23,233 snps then in SNPedia. Pooling all of his platforms provides 20,949 genotypes with at most 196 genotypes conflicting.
[edit] rs1333049
Since it's on the positive strand we wouldn't expect this
PGP via Complete Genomics
bzgrep rs1333049 ../Complete_Genomics_var_file.bz2 9664547 2 1 chr9 22125502 22125503 snp G 75 dbsnp.88:rs1333049 9664547 2 2 chr9 22125502 22125503 snp G 123 dbsnp.88:rs1333049
23andMe v2
zipgrep rs1333049 ~/dev/bots/insiders/inputs/genome_David_Duncan_20090607120612.zip genome_David_Duncan_20090607120612.txt:rs1333049 9 22115503 CC
grep rs1333049 ~/dev/bots/insiders/inputs/Duncan\ Affy\ 6.0.txt SNP_A-2191519 rs1333049 CC chr9 22115503
