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More options
1

Statistics and protein of selection button

1. Statistics and protein of selection button
Show sequence statistics.
 
2

Blast align consensus and selected sequences button

2. Blast align consensus and selected sequences button
Perform blast alignment with consensus and the selected sequence(s).
 
3

Align selected sequences

3. Align selected sequences
Select Optimized order to align the selected sequences in forward and reverse-complement directions, displaying the best result only. The second column (between the name of the file and the actual sequence) displays a green arrow pointing to the right when the sequence is displayed in forward direction and a red arrow pointing to the left when the reverse complement is displayed.
 
Select Original order to align the selected sequences using the current displayed direction. If the sequence is already displayed in reverse-complement, the sequence is NOT reset to forward direction before alignment.
 
4

Align all sequences

4. Align all sequences
The same as explained above in point 3 (Align selected sequences), but now using all sequences displayed in the sequence viewer.
 
5

Reset selected sequences button

5. Reset selected sequences button
Reset the selected sequences in the forward direction. It removes all previous offset computed during alignment.
 
6

Remove selected sequence button

6. Remove selected sequence button
Remove the selected sequence from the experiment. Warning: there is no undo!
 
7

Optimize order using first selected row as guide button

7. Optimize order using first selected row as guide button
In a multiple alignment result, it is possible that many sequences are displayed in reverse direction. In some cases, one sequence must remain in the forward direction and should be used to force all other sequences to align to its own content. This options keeps the first sequence in the current direction and adapt all others.
 
8

Reverse-complement selected sequences button

8. Reverse-complement selected sequences button
Replace the selected sequence by its reverse-complement content.
 
9

Move selected rows to top button

9. Move selected rows to top button
Move selected rows to the top of the sequence viewer, which may be necessary before aligning with the first sequence as a guide.
 
10

Move selected rows up button

10. Move selected rows up button
Move selected rows one place up.
 
11

Move selected rows down button

11. Move selected rows down button
Move selected rows one place down.
 
12

Move selected rows to bottom button

12. Move selected rows to bottom button
Move selected rows to the bottom of the sequence viewer.
 
13

Upper case selected sequences button

13. Upper case selected sequences button
Set the selected sequence completely to upper case. In general the sequences are written in uppercase and the changes made by hand are kept in lowercase.
 
14

Lower case selected sequences button

14. Lower case selected sequences button
Set the selected sequence completely to lower case. In general the sequences are written in uppercase and the changes made by hand are kept in lowercase.
 
15

Group selection button

15. Group selection button
Group sequences together. The advantage is that when a change is made to one of the sequences in the group, all the other sequences in the group are changed automatically too.
 
16

Ungroup selection button

16. Ungroup selection button
Ungroup the grouped sequences.
 
17

Enable all nucleotides button

17. Enable all nucleotides button
Enable all nucleotides.
 
18

Enable selected nucleotides button

18. Enable selected nucleotides button
Enable selected nucleotides.
 
19

Disable low confidence nucleotides button

19. Disable low confidence nucleotides button
Display in gray all nucleotides with a confidence below the confidence level (set in the Options dialog). They are automatically excluded from alignment computations.
 
20

Disable selected nucleotides button

20. Disable selected nucleotides button
Disable selected nucleotides.
 
21

Base caller

21. Base caller
Each nucleotide contains two different letters: the original nucleotide and the one computed from the trace wave. As different base-caller algorithms give different results, it may be necessary either to re-compute the most probable nucleotide, or to reset it to the original value.
 
Two algorithms are currently available in the Options dialog, the Average method and the Max value method. For more details on the algorithms click here.
 
22

Settings button

22. Settings button
Opens the Options dialog.