thank you Antonio,
sorry, how i can be aware of rate of the reads which aligned in multiple place on genome in tophat output?
Friends,
I aligned my reads in both bowtie2 and tophat. Now how I can see and compare the mapping result in two mentioned tools?
Thank you
Why do you want to do that ?. It is non sense..
TopHat will do a initial mapping using bowtie2 (so you get the same that using bowtie2 alone), and it will do a segmentation of the unmapped sequences to try a new mapping using bowtie2 again to detect spliced sequences
thank you Antonio,
sorry, how i can be aware of rate of the reads which aligned in multiple place on genome in tophat output?
If you have a sam/bam file, you can compare which mapping tool could align more number of reads. properly and improperly paired reads and overall number of reads aligned would help you.
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hello,
what version of bowtie you used in tophat? and what version of tophat you have used?
bowtie2 and tophat2