Table 1.
aWhen alternative splice forms were annotated, the longest open reading frame is shown.
bSome amplicons cover multiple exons.
cThe number of 384-well plates that were actually screened for a gene. Although the library consists of 16 384-well plates, we did not screen the complete library for all amplicons.
dOnly bases with a Phred score of ≥20 were included in the analysis.
ePercent of library screened is calculated by dividing the total number of exonic bases read by the multiplication of the open reading frame length of a gene with the total number of mutants (6144) in the library.
fThe number of non-G/C to A/T mutations is shown in parentheses.
gMutations that could not be reconfirmed in an independent PCR and resequencing assay. The number of non-G/C to A/T mutations is shown in parentheses.