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8.0 years ago
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Hi,
I have been running bowtie2 on RNA seq and eCLIP data a lot lately, and when I use the default global alignment option I get at best 45% of the reads aligned. The rates are better using local aignment, Is this a normal alignment rate? I used to run bowtie on DNA all the time and the rates were about 95%. Should I trust these results? Is it OK to use local alignm,ents instead?
Thanks!
why you don't use SOAP-splice, STAR or tophat (HISAT2 is alternative now)? splice-aware mapping is preferred.
In case of DNA "genomic" alignment sure Bowite will give you good result cause there is no splicing here
I am following a specific protocol that entails bowtie2 (I use STAR for other anylises)
Sounds like you should use a different analysis protocol then.
it is taken from Nature protocols
So?
That doesn't necessarily make it appropriate for this analysis. Which organism do you work on? Try to be as informative as possible.