Table 2.
Summary of NN Studies Reviewed
| Publication | Input | Output | Hidden Layer | |||
| Type | Coding | Type | Coding | Number Layers | Number Nodes | |
| Bhat et al. 1999 | Binary | 0 = absence of allele | Binary | 1/0/0 = unaffected | 1 | 15 |
| 1 = presence of allele | 0/1/0 = mildly affected | |||||
| 0/0/1 = severely affected | ||||||
| Bush et al 2005 | Discrete | -1, -1 = 1/1 genotype | Binary | 0 = unaffected | GP evolved | |
| 0, + 2 = 1/2 genotype | 1 = affected | |||||
| +1, -1 = 2/2 genotype | ||||||
| Costello et al. 2003 | Dicrete | Varied | Binary | 0 = unaffected | Multiple variations | |
| 1 = affected | ||||||
| Curtis et al. 2001 | Discrete | 0 = AA genotype | Binary | 0 = unaffected | 2 | 3 |
| 1 = AB genotype | 1 = affected | |||||
| 2 = BB genotype | ||||||
| Curtis 2007 | Discrete | 0 = AA genotype | Binary | 0 = unaffected | 2 | 3 |
| 1 = AB genotype | 1 = affected | |||||
| 2 = BB genotype | ||||||
| Giachino et al 2007 | Discrete and Continuous | Categorical values of genotypes and clinical features | Binary | 0 = unaffected | 1 | unknown |
| 1 = affected | ||||||
| Li et al. 1999 | Discrete | IBD sharing | Binary | 0/1 = concordant or not | Multiple variations | |
| +1= shared allele | 0/1 = affected or unaffected | |||||
| -1 = unshared allele | ||||||
| 0 = uninformative | ||||||
| Lin et al 2006 | Discrete | Categories of genotype combinations | Binary | 0 = non-response | Multiple variations | |
| 1 = response | ||||||
| Lucek and Ott 1997 | Binary | 0 = absence of allele | Binary | 4 nodes for each trait (20 total nodes) | 1 | 70 |
| 1 = presence of allele | 0 = quantitative trait off | |||||
| 1 = quantitative trait on | ||||||
| Lucek et al. 1998 | Discrete | IBD sharing | Binary | +1,+1 = target output | 1 | √220 |
| +1= shared allele | 0, +1 = noise | |||||
| -1 = unshared allele | ||||||
| 0 = uninformative | ||||||
| Marinov and Weeks 2001 | Discrete | IBD sharing | Binary | +1,+1 = target output | 1 | √220 |
| +1= shared allele | 0, +1 = noise | |||||
| -1 = unshared allele | ||||||
| 0 = uninformative | ||||||
| Matchenko-Shimko and Dube 2006 | Discrete | Three combinations of possible allele combinations, transformed to a 0–1 range | Binary | 0 = control | Multiple variations | |
| 1 = case | ||||||
| Motsinger et al (2006a) | Discrete | -1, -1 = 1/1 genotype | Binary | 0 = unaffected | GP Evolved | |
| 0, + 2 = 1/2 genotype | 1 = affected | |||||
| +1, -1 = 2/2 genotype | ||||||
| Motsinger et al (2006b) | Discrete | -1, -1 = 1/1 genotype | Binary | 0 = unaffected | GE Evolved | |
| 0, + 2 = 1/2 genotype | 1 = affected | |||||
| +1, -1 = 2/2 genotype | ||||||
| North et al 2003 | Discrete | 0 = AA genotype | Binary | 0 = unaffected | Multiple Variations | |
| 1 = AB genotype | 1 = affected | |||||
| 2 = BB genotype | ||||||
| Ott 2001 | Discrete | -1, -1 = 1/1 genotype | Binary | 0 = unaffected | NA | |
| 0, +2 = 1/2 genotype | 1 = affected | |||||
| +1, -1 = 2/2 genotype | ||||||
| Pankratz et al. 2001 | Discrete | IBD sharing | Binary | 1/1 = affected/affected | 1 | 4 |
| +1 = shared allele | 0/1 = affected/unaffected | |||||
| -1 = unshared allele | ||||||
| 0 = uninformative | ||||||
| Penco et al 2005 | Discrete | Categories of allele combinations at each genotype | Binary | 0 = unaffected | Multiple variations, including and evolutionary process | |
| 1 = affected | ||||||
| Pociot et al. 2004 | Discrete | Number of categories per sliding window | Binary | 0 = unaffected | Multiple variations | |
| 1 = affected | ||||||
| Ritchie et al. 2003 | Discrete | -1, -1 = 1/1 genotype | Binary | 0 = unaffected | GP evolved | |
| 0, + 2 = 1/2 genotype | 1 = affected | |||||
| +1, -1 = 2/2 genotype | ||||||
| Saccone et al. 1999 | Discrete | IBD sharing | Binary | 1/1 = affected/affected | 18 variations | |
| +1= shared allele | 0/1 = affected/unaffected | |||||
| -1 = unshared allele | ||||||
| 0 = uninformative | ||||||
| Serretti and Smeraldi 2004 | Discrete | SERPR*l/l = 1 | Binary | 0 = nonresponse | 1 | 7 |
| SERPR*l/s = 2 | 1 = response | |||||
| SERPR*s/s = 2 | ||||||
| TPH*C/C = 1 | ||||||
| TPH*C/A = 2 | ||||||
| TPH*A/A = 2 | ||||||
| Shoemaker et al. 2001 | Varied | Varied | Binary | 0 = unaffected | 1 | unknown |
| 1 = affected | ||||||
| Tomita et al 2004 | Discrete | Homozygous for major allele = (0.1, 0.1) | Binary | 0.9 = case | Multiple variations | |
| Heterozygous = (0.1, 0.9) | 0.1 = control | |||||
| Homozygous for minor allele = (0.9, 0.9) | ||||||
| Zandi et al. 2001 | Contin. | Pedigree-specific NPL scores | Binary | 1,1 = case pedigree | 15 variations | |
| 1,0 = control pedigree | ||||||