Table 2.
Analysis type† | ||||
---|---|---|---|---|
Variant* | WGS trio | Trio Segregation | Retnet genes | GWAS haplotype |
SNP | 14,215,442 | 487,324 | 74,852 | 9607 |
MNP | 822,020 | 11,856 | 4214 | 644 |
Insertion | 1,390,990 | 16,656 | 7439 | 636 |
Deletion | 1,279,028 | 22,134 | 6760 | 663 |
Mixed | 304,341 | 3314 | 1588 | 198 |
Total | 18,011,821 | 541,284 | 94,853 | 11,748 |
*Each alternate allele identified during variant calling is considered separately for tabulation of variant types, using the definitions at http://snpeff.sourceforge.net/SnpEff_manual.html#eff. †The analyses are based on feline reference genome sequence (V6.2). The GWAS identified an associated haplotype on cat chromosome E1. For Trio Segregation, the variants segregated with the disease phenotype as well, not just parent to offspring