Notice
1.10. Overlapping sliding window
- document 1 document 2 document 3
- niveau 1 niveau 2 niveau 3
Descriptif
We 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 produce an interesting result that is a prediction of the origin of replication of bacterial genomes. We have seen also that it may work for a large part of bacterial genomes but for some of them it doesn't work and this is the real life of bio informaticians. We have to deal with that. But, our algorithm was very visual. Now, we want to have a more quantitative approach to make apparent the bias in G, C or A, T and so on. Not only on the visual basis buton a more quantitative basis. Let's see how we can do that. We will change the algorithm a little bit. We are already familiar withthe notion of window. So, we know how to compute nucleotidefrequencies in a sliding window. Frequencies or number ofoccurrences, it's the same thing. So, what we will do is this newversion of the algorithm is we have a window onthe genomic sequence. On this window, we are able to compute the number of G and C. This should be very easy for you right now.
Thème
Documentation
Dans la même collection
-
1.8. Compressing the DNA walk
RechenmannFrançoisWe have written the algorithm for the circle DNA walk. Just a precision here: the kind of drawing we get has nothing to do with the physical drawing of the DNA molecule. It is a symbolic
-
1.3. DNA codes for genetic information
RechenmannFrançoisRemember at the heart of any cell,there is this very long molecule which is called a macromolecule for this reason, which is the DNA molecule. Now we will see that DNA molecules support what is called
-
1.6. GC and AT contents of DNA sequence
RechenmannFrançoisWe have designed our first algorithmfor counting nucleotides. Remember, what we have writtenin pseudo code is first declaration of variables. We have several integer variables that are variables which
-
1.1. The cell, atom of the living world
RechenmannFrançoisWelcome to this introduction to bioinformatics. We will speak of genomes and algorithms. More specifically, we will see how genetic information can be analysed by algorithms. In these five weeks to
-
1.9. Predicting the origin of DNA replication?
RechenmannFrançoisWe have seen a nice algorithm to draw, let's say, a DNA sequence. We will see that first, we have to correct a little bit this algorithm. And then we will see how such as imple algorithm can provide
-
1.4. What is an algorithm?
RechenmannFrançoisWe have seen that a genomic textcan be indeed a very long sequence of characters. And to interpret this sequence of characters, we will need to use computers. Using computers means writing program.
-
1.7. DNA walk
RechenmannFrançoisWe will now design a more graphical algorithm which is called "the DNA walk". We shall see what does it mean "DNA walk". Walk on to DNA. Something like that, yes. But first, just have a look again at
-
1.2. At the heart of the cell: the DNA macromolecule
RechenmannFrançoisDuring the last session, we saw how at the heart of the cell there's DNA in the nucleus, sometimes of cells, or directly in the cytoplasm of the bacteria. The DNA is what we call a macromolecule, that
-
1.5. Counting nucleotides
RechenmannFrançoisIn this session, don't panic. We will design our first algorithm. This algorithm is forcounting nucleotides. The idea here is that as an input,you have a sequence of nucleotides, of bases, of letters,
Avec les mêmes intervenants et intervenantes
-
1.5. Counting nucleotides
RechenmannFrançoisIn this session, don't panic. We will design our first algorithm. This algorithm is forcounting nucleotides. The idea here is that as an input,you have a sequence of nucleotides, of bases, of letters,
-
2.5. Implementing the genetic code
RechenmannFrançoisRemember we were designing our translation algorithm and since we are a bit lazy, we decided to make the hypothesis that there was the adequate function forimplementing the genetic code. It's now time
-
3.2. A simple algorithm for gene prediction
RechenmannFrançoisBased on the principle we statedin the last session, we will now write in pseudo code a firstalgorithm for locating genes on a bacterial genome. Remember first how this algorithm should work, we first
-
3.10. Gene prediction in eukaryotic genomes
RechenmannFrançoisIf 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
-
4.8. A recursive algorithm
RechenmannFrançoisWe have seen how we can computethe optimal cost, the ending node of our grid if we know the optimal cost of the three adjacent nodes. This is this computation scheme we can see here using the notation
-
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,
-
1.8. Compressing the DNA walk
RechenmannFrançoisWe have written the algorithm for the circle DNA walk. Just a precision here: the kind of drawing we get has nothing to do with the physical drawing of the DNA molecule. It is a symbolic
-
2.8. DNA sequencing
RechenmannFrançoisDuring the last session, I explained several times how it was important to increase the efficiency of sequences processing algorithm because sequences arevery long and there are large volumes of
-
3.5. Making the predictions more reliable
RechenmannFrançoisWe have got a bacterial gene predictor but the way this predictor works is rather crude and if we want to have more reliable results, we have to inject into this algorithmmore biological knowledge. We
-
4.6. A path is optimal if all its sub-paths are optimal
RechenmannFrançoisA sequence alignment between two sequences is a path in a grid. So that, an optimal sequence alignmentis an optimal path in the same grid. We'll see now that a property of this optimal path provides
-
5.1. The tree of life
RechenmannFrançoisWelcome to this fifth and last week of our course on genomes and algorithms that is the computer analysis of genetic information. During this week, we will firstsee what phylogenetic trees are and how
-
1.3. DNA codes for genetic information
RechenmannFrançoisRemember at the heart of any cell,there is this very long molecule which is called a macromolecule for this reason, which is the DNA molecule. Now we will see that DNA molecules support what is called
