Hello everybody,
I have a question which maybe you will find it naive, but for me your answer will be really helpful.
I’m interesting for the highly conserved elements among different genomes and I’m using the phastCons software to do that. My question is that.
In order to find the conserved elements why do I need a probabilistic model like the model that phastCons uses and not to identify the identical parts of each alignment blocks of the maf files?
I believe that I’m loosing something really important here. Thank you very much in advance for your time and your patience.
Vasilis.
So, the problem is that the alignment could not be accurate, thats why we are using probabilistic methods like phastCons? (I'm sorry for such childish questions, but I have a lack of biological background).
Broadly speaking, species that are more diverged from each other should have fewer true conserved sequences and lower quality alignments.
I don't recall the details of the phastCons algorithm right now, but I would assume that one of the factors it considers is the likelihood of seeing a conserved region based upon chance (depending on things like the size of the conserved region, the divergence within the conserved region, etc.)
Thank you very much, I believe that I'm starting to understand...