Table 1.
DF | Deviance | Resid. DF | Resid. Dev | F | p-value | |
---|---|---|---|---|---|---|
NULL | – | – | 17,855 | 2,201,873 | – | – |
Strain | 54 | 338,618 | 17,801 | 1,863,255 | 334.697 | <10−15 |
Targeted gene | 28 | 1,152,310 | 17,773 | 710,945 | 2196.584 | <10−15 |
Adults per well | 1 | 35,318 | 17,772 | 675,627 | 1885.113 | <10−15 |
Date | 1 | 2406 | 17,771 | 673,221 | 128.416 | <10−15 |
Strain × gene | 1512 | 349,415 | 16,259 | 323,806 | 12.334 | <10−15 |
Strain × adults per well | 54 | 6715 | 16,205 | 317,091 | 6.637 | <10−15 |
Gene × adults per well | 28 | 7358 | 16,177 | 309,732 | 14.026 | <10−15 |
The table rows report information associated with each term in our statistical model (see ‘Materials and methods’), which represent distinct sources for the variation we observed in embryonic lethality. All terms were highly significant, including the strain-by-gene interaction, which represents variation attributable to cryptic genetic modifiers that act gene-specifically. This term and the strain term, which represents variation attributable to informational modifiers affecting germline RNAi, explain similar amounts of variation, and together account for 31% of the total deviance.