Small RnA-Seq is a common means to interrogate the small RnA'ome or the full spectrum of small RnAs (<200 nucleotide length) of a biological system. A pivotal problem in NGS based small RNA analysis is identifying and quantifying the small RnA'ome constituent components. for example, small RNAs in the circulatory system (circulating RNAs) are potential disease biomarkers and their function is being actively investigated. Most existing nGS data analysis tools focus on the microRnA component and a few other small RNA types like piRNA, snRNA and snoRNA. A comprehensive platform is needed to interrogate the full small RnA'ome, a prerequisite for downstream data analysis. We present coMpSRA, a comprehensive modular stand-alone platform for identifying and quantifying small RnAs from small RnA sequencing data. coMpSRA contains prebuilt customizable standard RnA databases and sequence processing tools to enable turnkey basic small RNA analysis. We evaluated COMPSRA against comparable existing tools on small RNA sequencing data set from serum samples of 12 healthy human controls, and COMPSRA identified a greater diversity and abundance of small RNA molecules. coMpSRA is modular, stand-alone and integrates multiple customizable RnA databases and sequence processing tool and is distributed under the GnU General public License free to non-commercial registered users at https://github.com/cougarlj/coMpSRA. Small RNA sequencing (RNA-seq) technology was developed successfully based on special isolation methods and the RNA-seq technique, which facilitates the investigation of a comprehensive profile of small RNAs 1,2. One of the most important applications is to quantify small RNAs in the circulatory system (circulating RNAs). The human circulatory system contains various types of RNA molecules, including fragmental mRNA, miRNA, piRNA, snRNA, snoRNA, and some other non-coding sequences 3,4. Studies have shown the biomarker potential of circulating RNAs in cancer 5 , cardiovascular disease 6 , and asthma 7. Moreover, other types of DNA and RNA fragments discovered in the human circulating system have been implicated as potential causes of chronic disease 8,9. In anticipation of a continued growing number of circulating RNAs studies, a comprehensive and stable platform is needed to identify the RNA classification, RNA read counts, differential expression between case and control samples, including both human and non-human (e.g. microbiome) small RNAs (<200 nucleotide length). Previous efforts to characterize small RNAs have focused primarily on microRNAs (miRNAs). For instance, sRNAnalyzer is a comprehensive and customizable pipeline for the small RNA-seq data centred on microRNA (miRNA) profiling 10. sRNAtoolbox is a web-based small RNA research toolkit 11 and SeqCluster has started to focus on non-miRNAs by comparing the sequence similarity 12. Some efforts have begun to characterize the full spectrum of small RNAs of a biological system (the small RNA' ome), such as Oasis2, miRMaster and exceRpt 13-15. Oasis2 and miRMaster are...