This menu contains most of the functions that change the entries. Note that the changes will not be saved back to the orginal files until one of the save functions in the File menu is used (see the section called Save An Entry ...).
Open an edit window for each selected feature. This window has 4 parts:
At the top left is a selector for choosing the key of the feature. This only contains a subset of the legal keys. The subset can be changed by changing the common_keys option in the options file (see the section called common_keys in Chapter 2).
At the top right of the edit window is the location entry field. Artemis understands most of the EMBL location syntax, including joins, complements, ranges with non-exact ends (eg. (100.200)..>350) and references to other entries (eg. join(100..200,SPB23A1:100..200)).
The centre of the edit window contains the qualifier entry section. The qualifiers should be entered the in same way the appear in the feature table part of an EMBL entry, but without the leading FT and spaces.
The bottom of the window contains three buttons. The OK button will update the feature with the changes that have been made by the user and will then close the edit window. The Cancel button will discard the changes and then close the window. The Apply will make the changes, but will not close the window. Before any changes are made the location and the qualifiers are checked for formatting errors. Any errors will brought to the attention of the user through the use of annoying popup boxes. No changes will be performed until there are no errors.
Open an "raw" edit window for each selected feature.
Make a copy of each selected feature. Each new feature will be added just after the original in the same entry as the original.
Remove each selected feature from it's entry.
Remove an entry from Artemis. The original file that this entry came from (if any) will not be removed.
Move the selected features to another entry. A small window will open that allows the user to choose the destination entry.
Copy the selected features to another entry. A small window will open that allows the user to choose the destination entry.
For each of the selected features this function will attempt to move the start position to the first ATG in the feature. If there is no ATG in the first thirty percent of the bases of the feature the start position will be unchanged.
This works in the same way as "Trim Selected Features To Met", but will attempt to move the start position of the feature to the first TTG, ATG or GTG in the feature. As above it will only search the first thirty percent.
Ask for a gene name prefix (using a text requester), and then give a unique gene name to each CDS feature in the active entries using that prefix. For example if there are four CDS features with locations: "1..500", "complement(100..600)", "200..700" and "complement(300..800)", entering SPBC16A3 will give the four features these names: SPBC16A3.01, SPBC16A3.02c, SPBC16A3.03 and SPBC16A3.04c.
Check and fix the stop codons to all the selected features. For each feature if the last codon is a stop codon, then all is well, nothing further is done about the feature. If the last codon is not a stop codon, but the very next codon is a stop codon, then the end of the feature is moved three base forward. If both the last codon and the very next codon after the feature are not stop codons, the feature is selected, an error message is displayed and processing stops immediately.
Reverse and complement the sequence and all the features in all the entries (active and inactive).
Deletes the selected range of bases (if any) from both strands. The deletion will not proceed if the selected range overlaps any features.
Prompt the user for some bases to insert just before the selected bases. The deletion will not proceed if there is no selected range, but bases can be inserted anywhere in the sequence, including inside a feature. The same bases, reversed and complemented, will be inserted at the corresponding place on the opposite strand.