%1$s a.a. MW=%2$s
%1$s is already: %2$s
%GC
???(%1$s extra codons after stop)
>six cutter
1 frame 1 letter
1 frame 3 letter
1 Letter
2nd Strand
3 frame 1 letter
3 frame 3 letter
3 Letter
3 prime
5 prime
6 frame 1 letter
6 frame 3 letter
AA Info
ABI
About ApE
About ApE...
Above
absent (0)
Absent Enzymes
Absent Sites
Add
Add New
adjacent
Align DNA
Align Sequences
Align Sequences...
Align...
Alignment to
All
All Enzymes
Allowed keys:
also find rev-com of string
Amino Acids Data...
AND
Annotate Features using Library
any
ApE: File not saved
Are you sure you want to delete these %1$s groups?
as amino acid
as literal
Background
Band:
bases.
Below
Binding
BLAST DNA at NCBI...
Blast DNA at Wormbase...
BLAST Program:
BLAST Sequences at NCBI...
BLAST Sequences at Wormbase...
Blocks:
blunt
Both
Bottom
BP Reaction (1-2)
BP Reaction (1-2-2-1)
BP Reaction (1-4)
BP Reaction (1-5)
BP Reaction (2-3)
BP Reaction (3-2)
BP Reaction (4-1)
BP Reaction (4-3)
BP Reaction (5-2)
BP Reaction (5-4)
Bring All to Front
C. briggsae genomic
C. briggsae proteins (Brigpep)
C. elegans ESTs
C. elegans genomic
C. elegans proteins (WormPep)
Cancel
Can't Undo
case sensitive
Center Feature Labels on Graphic Map
Change Case
Change Directory
Change to Lowercase
Change to Uppercase
character every
Characters/line:
Chose a Recombination Prototype
circular
Circular<->Linear
clear all
Clear Features
Clear Find
Clear Find Highlighting
Clear Highlight
Clear Highlighting
Click to Save File
Close
Close Selection Dialog
Code:
Codon Spacing
Color
Columns:
Comment Height
Comment:
Configure Text Map...
Consecutive bases: 
Convert to lowercase
Convert to UPPERCASE
Copy
Copy All as Genbank
Copy as Metafile
Copy Complement (NOT A GOOD IDEA)
Copy Highlight
Copy Highlighting
Copy Highlighting from Sequence
Copy Metafile
Copy Rev-Com
Copy Reverse (NOT A GOOD IDEA)
Copy Special
Copy to Clipboard
Copy Translated
Copy Translated Rev-Com
Copy Uppercase Translated
Copy Uppercase Translated Rev-Com
Create Default Enzyme File
Create Default Feature File
Cut
Cut Rev-Com
Cut to Clipboard
Dam blocked:
Dam/Dcm default
Database:
Dcm blocked:
Default DNA Directory:
Default Enzyme Directory:
Default Feature Directory:
Default File Extension
degenerate
degenerate cut
Delete
Delete Enzyme Groups...
Delete Groups...
Delete Selected Enzymes
De-select
Difference...
Digest
Digestion
Digestion Window
DNA
DNA:
Do you want to exit?
Do you want to save the changes you made to
Done
Download sequences from NCBI...
Draw Connectors in Graphic Map
Duplicate All
Duplicate File
Duplicate Full Sequence
Duplicate Selection
Edit
Edit enzyme:
Edit Favorites
Edit Feature
Edit Feature Definition...
Edit Feature Library...
Edit Feature...
Edit Features...
Edit Groups and Methylation
Edit Ladders...
Edit...
End
Entrez Query...
Enzyme highlight
Enzyme Highlight Bold
Enzyme Highlight Underline
Enzyme Selection Dialog
Enzyme Selection...
Enzyme Selector...
Enzyme:
Enzymes
Enzymes:
equal to
Exit
Expect Threshold:
Expect:
Export as SCF
Export Internal Feature File
Favorites
Feature default (fwd)
Feature default (rev)
Feature Display Properties
Feature type:
Features
Features List
File
File Comment
File Info
File Info:
File is not writable, probably locked.
File is not writable.
Files
Filetypes
Find Again
Find in
Find Next
Find ORFs starting with:
Find Prev
Find Previous
Find Primer
Find Primers
Find Primers...
Find(forward)
Find(reverse)
Find...
First Position
five cutter
Follows Last Opened File
Foreground
Format:
Forward color:
four cutter
From
from
From %1$s to %2$s.
Gap Ext. Penalty:
Gap Penalty:
Gaps
GC clamp: 
General
Genes
Graphic font:
Graphic Map
Graphic Map +U
greater than
Groups:
Help
Heterodimer: 
Highlight
Highlight All
Highlight Features
Highlight Selected Enzymes
Ig
Image
Import Enzymes From DNA Strider...
Index Line
insert@
Jorg Enzymes
Jump to
Jump To...
Jump to:
Key substitutions:
Ladder
Ladder:
Ladders...
Last DNA window
Left
Length
length
Length: 
less than
Line Numbers:
Line Width:
linear
Linearize @ insert site
List
List enzyme + recognition sequences
List enzymes
List enzymes + #sites
List enzymes + site positions
List Enzymes...
List Features
Locale:
location
Lock/Unlock
Low Complexity Filter
Lower
Lowercase
Lowercase to +
Map
Mass %
Matches
Max hits:
Maximum
Mem Recall
Menu
Menu (selected)
Methylation
Minimize
Minimum
Misc
Mismatch Penalty:
Mismatches
Multiple Group Delete
Multi-site LR Reaction (4-1-2)
Multi-site Pro LR Reaction (1-4-3-2)
Multi-site Pro LR Reaction (1-5-2)
Multi-site Pro LR Reaction (1-5-4-3-2)
Mutlti-site LR Reaction (4-1-2-3)
Name
Name, #Sites
Name, Site, #Sites, Positions
Name:
New
New DNA
New DNA from basecalls
New Enzyme
New Enzyme Group...
New Enzyme...
New Feature
New Feature in Library...
New Feature...
New File
New Group...
No Enzyme Color
No enzymes selected, searching all enzymes.
No sites Found
No Translation
None
NOT
Not enough sequence selected for BLASTing
not unique (>1)
Numbers
N-W align all
N-W max:
OK
Open
Open An Enzyme File
open ApE Features file
Open DNA Strider enzymes file
Open Feature Library...
Open Features File
Open File
Open Group List File
Open new enzymes file
Open Recent Files
Open...
OR
ORF
ORF map
ORFs
Orientation:
Page Setup
Paste
Paste from Clipboard
Paste Rev-Com
Perform Action
Potential
Preferences...
present (>0)
Primer (5'-->3') 
Primer (nM):
Print
Print lines per page:
Print Text with color Formatting (slower)
Print with Color Formatting
Printing will occur on your default printer:\n%1$s
Printing...
Program
Query
Query Result
Quick Lists
Raise
Raise Parent
Raise Window 1
Raise Window 2
Read Groups File...
Recently used files list
Recolor
Recombination Reaction Product
Recombination Reaction...
Recombination Tool...
Redo
Rename
Repeats
Restore Program Defaults
Rev-Com
Reverse color:
Reverse Complement
Reverse-Complement
Right
RNA
Run began:
Run ended:
Run Query
Salt (mM):
Same
Sample:
Save
Save As
Save As Text File
Save As...
Save Changes
Save Changes As...
Save current enzymes as Default
Save Enhanced Metafile...
Save enzymes file
Save File
Save File As...
Save Files in Format:
Save Image
Save Window
Save Window as EPS image
Saved
Scale
Scale:
Scaling:
Scan on Close
Search Strand
Searching %1$s selected enzymes.
Searching for fixed fonts on the system, please wait...
Second Position
Sel to Mem
Select
Select All
Select Enzymes
Select from
Select from to
Select From-To
Select From-To...
Selected DNA only
Selected Enzymes
Selected Enzymes Only
Selected Sites
Selection Only
Selection Translate
Selection: 
Self complement: 
self/other(max adj 3')
Sequence
Set Origin
Shift:
Show
Show File Comment
Show/Hide
Signals
Silent Sites
Single-site LR Reaction (1-2)
Site
Site Usage
Site, Name
Site:
site1
site2
six cutter
Size
Skip Blank Fields in Genbank
Sort by:
Speak Texts
Speed (ms):
Stacking Order
Standard Genetic Code
Standard Genetic Code...
Start
Start Speaking
Start/Stop Speak Text...
Stop Speaking
Strict Genbank Format
Text
Text (background)
Text (selected)
Text font:
Text Map
Text Map Item Order...
Text Map...
There is no text selected.
Tm(°C)
to
Toggle Selected Only
Tools
Top
total
Translate Selection
Translate...
Translation
Translation by:
Translation:
type
Typing
Unattempted
Undo
unique (1)
Unique Enzymes
Unique Sites
UPPER<->lower
UPPER<->lower Exchange
Uppercase
Uppercase as Genes
Usage
Use left arrow to slow, right to accelerate, space to start and stop.
Variations
Verify Methylation...
Warn if Changing File Formats
Window
Window:
Windows