find_star_sites
Where the given enzymes could ALSO cut the open plasmid under non-standard conditions, from REBASE's own star-activity list and its one-base rule. Not cut sites: these need low ionic strength, high pH, Mn²⁺ for Mg²⁺, glycerol, DMSO or some detergents, and are what turns an over-digested reaction into a band pattern that reads as the wrong clone.
Input Schema
| Name | Required | Description | Default |
|---|---|---|---|
| _files | No | The project: record references shaped like _subject. Their records become library documents a tool names in sequences/parts/document; a trace or alignment is found by file name. | |
| enzymes | Yes | enzymes to check — resolved against the bundled cut catalog (REBASE spellings; smaller than the REBASE dossier the editor shows). Left unset, the run uses your active enzyme collection. | |
| _subject | No | The record to act on: exactly one of sequence, accession (+source), sample (an id from list_samples) or file ({name, text} or {name, base64}); record_index picks one record of several. |
Output Schema
| Name | Required | Description | Default |
|---|---|---|---|
| sites | Yes | total possible star sites across the enzymes REBASE has examined | |
| enzymes | Yes | per enzyme: whether REBASE examined it, and its possible star sites here | |
| unexamined | Yes | how many of the enzymes REBASE has NOT tested for star activity |