Team:VT-ENSIMAG/Methods
From 2010.igem.org
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=Database= | =Database= | ||
=Test= | =Test= | ||
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<tr> | <tr> | ||
- | < | + | <td rowspan="2" style="border-style: solid; border-width: 1px 1px 1px 1px" align="center"> |
- | + | ''' Database''' | |
- | < | + | <td style="border-style: solid; border-width: 1px 1px 1px 1px"> |
- | + | '''SAT/NSAT''' | |
- | < | + | <br> |
- | + | Both Select Agent and Toxins and non-Select Agent and Toxins were added to the DB for test sequences. [[Team:VT-ENSIMAG/Table1|Click here]] to find out more about Select Agent and Toxins. | |
+ | <td rowspan="2" style="border-style: solid; border-width: 1px 1px 1px 1px" width="100" align="center"> | ||
+ | [[Team:VT-ENSIMAG/Result1|Results]] | ||
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- | + | '''Housekeeping''' | |
+ | <br> | ||
+ | Housekeeping genes were added to the database for both Select and non-Select Agents and Toxins to determine whether the screening software can effectively screen them. [[Team:VT-ENSIMAG/Table2|Click here]] to find out more about housekeeping genes. | ||
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- | + | <td style="border-style: solid; border-width: 1px 1px 1px 1px" rowspan="3" align="center"> | |
- | < | + | ''' Modifications''' |
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- | < | + | '''Intervening Sequence''' |
- | + | <br> | |
+ | An intervening sequence is an SAT sequence hidden within a larger, benign sequence. These modified sequences were constructed to determine whether the program can find hidden sequences. [[Team:VT-ENSIMAG/Table3|Click here]] to learn more about how these sequences were made. | ||
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+ | <td style="border-style: solid; border-width: 1px 1px 1px 1px" rowspan="3" align="center"> | ||
+ | [[Team:VT-ENSIMAG/Result2|Results]] | ||
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<tr> | <tr> | ||
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- | + | '''Random Mutations''' | |
+ | <br> | ||
+ | A random mutation sequence contains a defined number of mutations to resemble single nucleotide polymorphisms (SNPs). They were designed to test how effectively the software screens when sequence alignment parameters are varied. [[Team:VT-ENSIMAG/Table4|Click here]] to learn more about how these sequences were made. | ||
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+ | '''Degeneracy''' | ||
+ | <br> | ||
+ | Degenerate, or synonymous, sequences have different nucleotide sequences but encode the same protein. These sequences were screened to determine whether it is really necessary to align both the nucleotide and translated amino acids. [[Team:VT-ENSIMAG/Table5|Click here]] to learn more about how these sequences were made. | ||
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+ | <tr> | ||
+ | <td style="border-style: solid; border-width: 1px 1px 1px 1px" rowspan="3" align="center"> | ||
+ | ''' Tests''' | ||
+ | <td style="border-style: solid; border-width: 1px 1px 1px 1px"> | ||
+ | '''Keyword List''' | ||
+ | <br> | ||
+ | The keyword list is used to determine if the “Best Match” is to an SAT or not. This test is designed to show how the keyword lists affects the outcome of our program. [[Team:VT-ENSIMAG/Table6|Click here]] to see more about how the keyword list and test. | ||
+ | <td style="border-style: solid; border-width: 1px 1px 1px 1px" rowspan="3" align="center"> | ||
+ | [[Team:VT-ENSIMAG/Result3|Results]] | ||
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+ | <td style="border-style: solid; border-width: 1px 1px 1px 1px"> | ||
+ | '''BLAST Parameters''' | ||
+ | <br> | ||
+ | BLAST has parameters that affect the resulting sequence alignments. This test is used to identify the affects of various BLAST parameter combinations. [[Team:VT-ENSIMAG/Table7|Click here]] to learn about the various BLAST parameters and how they may affect sequence screening. | ||
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+ | '''Sequence Length''' | ||
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+ | Sequence length has the potential to affect our programs speed. This test tests the impact of sequence length on the programs speed. [[Team:VT-ENSIMAG/Table8|Click here]] to learn more about how the test was performed. | ||
</table> | </table> | ||
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Revision as of 21:15, 4 August 2010
Methods
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BLASTThe federal guideline suggest explicitly to use the software Blast for sequence alignement (See more). Sofware implementationDatabaseTest
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