This page is based on more typical target prediction programs used to
predict targets of small RNA sequences such as microRNAs - BUT, since no
genome may be available or since you may have a genomic sequence that you
would like to assess for targets of small RNAs, we have developed a "reverse
target prediction" algorithm. In this case, the user enters a genomic
sequence, and then picks a set of small RNAs to compare against that
sequence. In some cases, it may be possible to use this page with the output
of another of our small RNA analysis pages. Because this is a
computationally intensive search (due to the mismatches permitted for miRNA
targets), we limit the size of the input sequence. The result will be a set
of small RNAs that match the input sequence with the characteristics of a
miRNA.
Mismatches and wobbles (G:U mismatches) are given a score based on their
position on the alignment between the input sequence and the putative
small RNA targeting it. Final scores are provided as sum of single scores
over the entire alignment. Gapped alignments are not allowed.
Default settings are indicated below in the
scoring system table. However, customized criteria can be entered by the
user.
Also to minimize the computational time, we require that the user select
smaller molecules (18-22 nt) or larger molecules (>22 nt). Since miRNAs are
usually 20-22 nt, we recommend using the smaller class.
Please enter the genomic sequence into the box below. Fasta format should be
used; the ">" symbol followed by the sequence name should precede the
genomic sequence.
Please select the small RNA library from the following lists for comparison to the DNA sequence that you have entered above.
Select Species:
Small RNA length:
18-22 bp
Scoring system:
Default
Enter maximum number of mismatches allowed (inclusive of all non-canonical Watson & Crick pairings):
Enter value for wobble pairing in:
2 to 7 nt positions
10 to 11 nt positions
Enter value for wobble pairing in all other positions:
Enter value for other non-canonical Watson & Crick pairing in:
2 to 7 nt positions
10 to 11 nt positions
Enter value for other non-canonical Watson & Crick pairing in all other positions:
Do you want the best score in 20 consecutive nucleotides (when length > 20):
No
Filter:
10/11 nt positions - perfect match required
2 to 9 nt positions - no more than one mismatch allowed (forces most mismatches into 12 to 21 nt positions)
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