Hi Devon,
Thank you very much for your detailed explanations, all of which are helpful for my work.
Hi everyone,
I actually have three minor questions about bowtie. I wrote a run.sh file as follows:
bowtie2-build rrna.fa rRNA
bowtie2 --very-sensitive -x rRNA -f reads.fa --un a.fa
bowtie2-build genome.fa GENO
bowtie2 --very-sensitive -x GENO -f a.fa --un b.fa
However, when running bash run.sh, I was encountered a problem as follows. This is my first question.
Could not locate a Bowtie index corresponding to basename "GENO"
Error: Encountered internal Bowtie 2 exception (#1)
My second question is related to bowtie --very-sensitive option. Does this option map more reads on the genome?
My third question is about bowtie vs tophat. My understanding is: bowtie can not detect exon splicing, so abandoned some mapping reads; in contrast, Tophat overcomes this problem and enables more reads mapping on genome. Is my understanding right?
THANK YOU very much!
--very-sensitive and --very-sensitive-local presets mostly affect reads that can align with a high edit distance. However, since the seed size changes with these, you may occasionally exhaust the number of seed extensions before finding the actual best alignment (this is true with any setting, but is more likely to occur as the seed size is decreased). Having said that, you'll typically get a few more reads mapped with these settings, though it'll take longer to do so.Log in to answer this question.