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3.10. Gene prediction in eukaryotic genomes
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If it is possible to have verygood predictions for bacterial genes, it's certainly not the caseyet for eukaryotic genomes. Eukaryotic cells have manydifferences in comparison to prokaryotic cells. You rememberthe existence of a nucleus and you also remember on one ofthe schemes in the first week that there are more structureswithin a eukaryotic cell. But the differences lie also inthe organization of the genomes. In eukaryotic genomes, the so-calledintergenic regions are very long. Intergenic regions are theregions which separate genes. A bacterial genome is very denseindeed, if you put your fingers somewhere on the genome, if itwas possible of course, it would be on the gene. If you do the sameon a eukaryotic genome, the probability is very very very highthat it is on an intergenic region. Indeed if you take the exampleof the human genome, less than 5% of the sequences of a human genome are made up of genes, 95 % of the humangenomes are not genes. What are they? This isstill an open question. Years ago a biologist spoke about germDNA to say, well DNA which is useless. Now the feeling is somewhat different,it certainly has a reason to exist. We understand some of thesereasons but not all.
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3.5. Making the predictions more reliable
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3.8. Probabilistic methods
RechenmannFrançoisUp to now, to predict our gene,we only rely on the process of searching certain strings or patterns. In order to further improve our gene predictor, the idea is to use, to rely onprobabilistic methods
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3.3. Searching for start and stop codons
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3.6. Boyer-Moore algorithm
RechenmannFrançoisWe have seen how we can make gene predictions more reliable through searching for all the patterns,all the occurrences of patterns. We have seen, for example, howif we locate the RBS, Ribosome
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3.1. All genes end on a stop codon
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3.9. Benchmarking the prediction methods
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3.4. Predicting all the genes in a sequence
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3.7. Index and suffix trees
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3.2. A simple algorithm for gene prediction
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1.2. At the heart of the cell: the DNA macromolecule
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1.10. Overlapping sliding window
RechenmannFrançoisWe have made some drawings along a genomic sequence. And we have seen that although the algorithm is quite simple, even if some points of the algorithmare bit trickier than the others, we were able to
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2.3. The genetic code
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3.6. Boyer-Moore algorithm
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4.4. Aligning sequences is an optimization problem
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5.2. The tree, an abstract object
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1.5. Counting nucleotides
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2.4. A translation algorithm
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3.9. Benchmarking the prediction methods
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4.8. A recursive algorithm
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5.6. The diversity of bioinformatics algorithms
RechenmannFrançoisIn this course, we have seen a very little set of bioinformatic algorithms. There exist numerous various algorithms in bioinformatics which deal with a large span of classes of problems. For example,