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. 2019 Oct 24;15:119. doi: 10.1186/s13007-019-0500-2

Table 3.

Evaluation of editing accuracy for TaABCC6 and TaNFXL1 using homoeologs with perfect match (A) or mismatched bases (B) to the sgRNA

(A)
Gene On-target gene IDa Total mapped readsb Reads with modifications Editing frequencyc
TaABCC6 TraesCS2A01G451300 14,718 1059 7.2
TraesCS2D01G451100 5337 235 4.4
TaNFXL1 (edited by crCas9) TraesCS7A01G518800 1780 294 16.50
TraesCS7B01G434700 26,991 4142 15.30
TaNFXL1 (edited by pcoCas9) TraesCS7A01G518800 3479 357 10.3
TraesCS7B01G434700 22,519 1062 4.7
(B)
Gene Off-target Gene IDa Total mapped readsb Reads with modifications Editing frequencyc
Edited by crCas9 Edited by pcoCas9
TaABCC6 TraesCS2B01G472800 15205 N/A 252 1.7
TraesCS2A01G451500 1722 N/A 0 < 0.06
TraesCS2D01G451300 1987 N/A 0 < 0.05
TaNFXL1 TraesCS7D01G688900LC 2621 2887 0 < 0.04

N/A not applicable

aOnly genes for which a specific fragment was PCR-amplified and sequenced are presented here. See Additional file 1 for more details

bThe number of reads mapping perfectly to the corresponding target or off-target sequence

cEditing frequency (%) = (reads with modification/(mapped reads + reads with modification)) × 100