TABLE 1.
Comparison of RT mutation frequencies versus WT: all classes of mutant lacZα sequencesc
Enzyme ID | Mutation frequencya | Mutation rateb | Raw (FET) P value | BH (FDR)-adjusted P value | BH significance |
---|---|---|---|---|---|
WT | 451/205,171 | 1.4 × 10−5 | |||
Y115F | 524/93,725 | 3.7 × 10−5 | <0.0001 | <0.0001 | **** |
Q151M | 537/209,064 | 1.7 × 10−5 | 0.0154 | 0.0177 | * |
M184I | 479/150,110 | 2.1 × 10−5 | <0.0001 | <0.0001 | **** |
M184V | 466/172,601 | 1.8 × 10−5 | 0.0020 | 0.0027 | ** |
Mutation frequency data represent the number of mutant lacZα sequences divided by the total number of recovered clones.
Mutation rate data represent the mutation frequency divided by the size of the lacZα target sequence. Because the data were obtained with a one-round vector, the rate data were calculated as mutations/bp/generation.
Raw (FET) data represent P values of the significance of the results of comparisons to the WT by Fischer's exact test (FET). To control for compounding type I error in these multiple comparisons, the Benjamini-Hochberg (BH) false-discovery-rate (FDR) corrections to significance calculations were applied to the raw (FET) P values where a single asterisk (*) represents 0.05 or less, two asterisks (**) represent 0.01 or less, three asterisks (***) represent 0.001 or less, and four asterisks (****) represent 0.0001 or less. ID, identifier.