The BLAST (Basic Local Alignment Search Tool) tool compares input sequences to PlantGenIE sequence databases to identify homologous sequence matches.
Simply paste your sequence (with or without a FASTA header) into the Query Sequence input text box. Alternative you can retrieve a transcript sequence by entering a gene ID into the Load example text box, or you can upload a sequence file (Less than 100 MB) using the upload file function. Having used one of these input options, click and select the desired dataset from the lists of available BLAST databases. Finally click the BLAST! button at the bottom of the page.
PlantGenIE BLAST uses standard default NCBI BLAST options. However users can change the following advanced options:
|Scoring matrix||Substitution matrix that determines the cost of each possible residue mismatch between query and target sequence. See BLAST substitution matrices for more information.|
|Filtering||Whether to remove low complexity regions from the query sequence.|
|E-value cutoff||The maximum expectation value of retained alignments.|
|Query genetic code||Genetic code to be used in blastx translation of the query.|
|DB genetic code||Genetic code to be used in blastx translation of the datasets.|
|Frame shift penalty||Out-of-frame gapping (blastx, tblastn only) [Integer] default = 0.|
|Number of results||The maximum number of results to return.|
The BLAST Results page will be automatically reloaded until the search results are successfully retrieved. BLAST results are organized into a table containing Query ID, Hit ID, Average bit score (top), Average e-value (lowest), Average identity (av. similarity) and Links. Clickable BLAST results display the corresponding region of identified homology within the GBrowse tool, where the matching region is shown.
The BLAST tool uses public genome assemblies, early release de novo assemblies from UPSC and data from [Phytozome] (http://www.phytozome.net/) and Plaza.