I'm using SPAdes to do de novo transcriptome assembly using RNA-seq (from Illumina). However, the new version SPAdes 3.14.1 has excluded the read error correction step for RNA-seq. So I want to use the BayesHammer which comes with SPAdes to do the error correction. However, I can't find the usage of BayesHammer. I want to ask if this can be used as a standalone tool for RNA-seq. Any one please can you give me any instructions. Thanks a lot.