Thanks, very helpful. Are you aware of any comparison (paper or post) between STAR and lets say bowtie2 or bwa in case of bacterial data?
Hi Biostars,
Is it fine to use STAR for bacterial data (no splicing)? Any comments/suggestions are highly appreciated.
Thanks
1 answer
It should work but you need to specify --alignIntronMax 1 to force STAR to avoid splice alignments.
Also during the genome index generation step you should put --genomeSAindexNbases to min(14, log2(GenomeLength)/2 - 1) if your bacterial genome of interest is relatively small. GenomeLength is in base pairs
No don't know any benchmarking for bacterial genomes
I've made quite a few comparisons, but haven't published them yet.
Briefly, bacterial genomes are quite easy to map to - so uniquely mapped reads don't differ much between bwa/bowtie2/STAR/etc. However STAR/hisat2 are a lot better in reporting multimappers, which could be interesting for highly repetitive genomes like Nesseria etc.
I think the formula might be over-estimating the value a bit. The number min(14, log2(GenomeLength)/2 - 1) for something like Ecoli/Salmonella should be approximately 10, yet sometimes I get segfaults with this setting. Changing it to 8 fixes everything.
Hi, Nicolas. What do you understand by "relatively small genomes"? I am dealing with data that ranges from 1,02 Mb to 9,56 Mb. Biologically, I've read publications that indicate 2 Mb as a common threshold but I'm guessing that the impact of the parameter won't attend to considerations of that nature when computing. Thanks in advance.
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