Thank you RamRS.
So shall I perform some kind of assembly of the metatranscriptome reads before doing the BLAST? Can BLAST give me also the expression profiles of each detected bacterial genes?
Thanks!
Hi,
I have a very basic question but it confused me a little bit.
For a metatranscriptome data, we can compare it with the NCBI prokaryote genome collections. Shall I use bowtie, tophat these kinds of mapping tools here, or just use BLAST here? What's the difference between this two kinds of tools? What kind of different downstream analysis would be available only for one tool?
Thanks!
Hi,
TopHat and Bowtie are aligners - they align short sequences, typically reads, to reference genomes. You are comparing a metatranscriptome to a genome. BLAST should be better suited for you.
Thank you RamRS.
So shall I perform some kind of assembly of the metatranscriptome reads before doing the BLAST? Can BLAST give me also the expression profiles of each detected bacterial genes?
Thanks!
If you have contigs, you will be able to detect more gene sequences, since the contigs are bigger than reads. If you want to do gene prediction, I will vote for doing a little assembly first.
Hi, I really like your idea!
So if we want to get the expression profile of each microbial genes to see the dynamics, shall we use bowtie/tophat plus cufflinks, or we can use BLAST tools for this purpose?
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