|
Comparison of programs for the detection of repetitive subsequences in proteins |
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| Program |
Method used |
Detection of degenerate repeats |
Calculation of a P-Value |
Analysis of whole Proteomes |
%Hits found in SwissProt |
Detection of T. brucei procyclin1 |
|
|
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| Reptile |
Hashing2 |
No |
Yes |
Yes |
153 |
Yes |
| REP [2] |
Profiles of known repeats |
Yes |
No |
No |
1.1 |
No |
| RADAR [5] |
Alignment |
Yes |
No |
No |
28 |
Yes |
| REPRO [7] |
Alignment |
Yes |
No |
No |
n.a. |
Yes |
| Internal Repeats finder [8] |
Alignment |
Yes |
Yes |
No |
14 |
No |
| TRIPS [9] |
Fourier transform |
Yes |
No |
No |
12 |
No |
| RepSeq [10] |
Hashing |
Yes |
Yes |
Yes |
n.a. |
Yes |
| ProtRepeatsDB [11] |
Mixed |
Yes |
Yes |
Yes |
n.a. |
Yes |
| Repper [12] |
Fourier transform |
Yes |
No |
No |
n.a. |
No |
|
1The T. brucei surface protein (GenBank accession AAK62893) with five GPEET repeats [25] was used for benchmarking. 2Word count using a hash table. 3Using P < 0.001 (same as for Internal Repeats Finder). | ||||||
Fankhauser et al. Proteome Science 2007 5:20 doi:10.1186/1477-5956-5-20 |
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