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. 2019 Apr 10;7:e6710. doi: 10.7717/peerj.6710

Table 2. Table describing the supporting features of RAPID (Column headers in Table 1).

Supporting feature Description
Contaminant removal Is there an option to remove set of contaminants (microbial, ribosomal, etc.) from the read files?
Supports other aligners Does the tool support alignment files from other tools, instead of performing their own alignment?
User-defined gene/region Could the user specify a list of regions to perform downstream analysis?
Knockdown corrected normalization Does the tool enable multiple-sample comparison by facilitating normalization techniques specific to sRNA knockdown studies?
Offline Can the tool be used offline?
Hardcoded genomes Is the tool generic? i.e., Is the tool’s ability somehow limited to a set of pre-defined genomes?
Quantitative, and Qualitative Plots Does the tool support informative plots to gain understanding of the analyzed data (MDS=multi-dimensional scaling, PCA= principal component analysis)
Multi-sample comparison plots Does the tool provide a comprehensive view of multiple samples (not just differential analysis)? For instance, how does the read distribution vary across multiple samples in different genes of interest?
Differential analysis Is the tool equipped with modules to perform pairwise differential analysis?
Enrichment analysis support Is there any support to perform functional enrichment within the tool
Interactive interface Does the tool have an interactive interface, or plots?
miRNA or piRNA specific? Is the tool specific to analyze miRNA or piRNA only?