I have small rna data to assembly,there is no reference sequence .the length is18-28nt.
The result like the result of cap3 . Like this
>1
ACCTTTTTTTTTTACCCCT
>2
CTTTTTTTTTTACCCCTACAC
Result
>contig1
ACCTTTTTTTTTTACCCCTACAC
which program is better?
You will have to improve this question to get an answer. "Which soft is better" does not make sense. What is "soft"?
your reads are shorter than 28nt?
reads from short rna libraries often contain a very high percentage of adapter sequence, so in case you were running 36bp protocol it's not surprising to end up with 18-28bp soft-trimmed reads
Yes,the clean reads.