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Table 2 Details of the 19 base substitutions called at the first screening in the control sample

From: Mutation assay using single-molecule real-time (SMRTTM) sequencing technology

Reference position

Reference

Forward read

Reverse read

Comment

Judgement

p-value**

Most dominant allele

Coverage

Read count

p-value*

Most dominant allele

Coverage

Read count

p-value*

999271

C

C

33

23

3.9E-20

T

36

30

5.5E-31

 

Mismatch

0

4778252

T

T

17

16

9.1E-19

A

19

19

4.4E-23

 

Mismatch

0

3355477

0047

C

13

12

4.4E-14

G

11

10

1.0E-11

 

Mismatch

1.0E-11

536849

C

C

9

9

2.5E-11

T

9

9

2.5E-11

 

Mismatch

5.0E-11

1051080

G

A

10

9

1.6E-10

G

10

9

1.6E-10

 

Mismatch

3.1E-10

3287776

A

T

11

8

8.2E-08

A

12

11

6.7E-13

 

Mismatch

8.2E-08

3823422

C

C

7

4

5.7E-03

G

11

10

1.0E-11

 

Mismatch

5.7E-03

316363

G

        

edge of map

No

 

694963

C

        

edge of map

No

 

918766

G

        

edge of map

No

 

1922859

C

        

edge of map

No

 

4423790

C

        

edge of map

No

 

4144134

C

        

No mutation

No

 

4515279

C

        

No mutation

No

 

290717

C

        

original allele

No

 

1760048

A

        

original allele

No

 

1760052

A

        

original allele

No

 

3741045

T

        

original allele

No

 

4099877

G

        

original allele

No

 
  1. *Probability that the real allele is not the most dominant allele
  2. **Probability that the Judgement is not correct