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README.md

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 # ViralConsensus
 ViralConsensus is a fast and memory-efficient tool for calling viral consensus genome sequences directly from read alignment data. ViralConsensus is orders of magnitude faster and more memory-efficient than existing methods. Further, unlike existing methods, ViralConsensus can pipe data directly from a read mapper via standard input and performs viral consensus calling on-the-fly, making it an ideal tool for viral sequencing pipelines.
 
+To run ViralConsensus, you can either install the command-line tool (instructions below), or you can try out the [web app](https://niema.net/ViralConsensus) created by my student, [Daniel Ji](https://www.linkedin.com/in/danielji26), which is a complete WebAssembly port of ViralConsensus (meaning it runs fully client-side in your own web browser!). The web app works well for reasonably small datasets, but for larger datasets, you will want to use the command-line tool.
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 # Installation
 ViralConsensus is written in C++ and depends on htslib. First, you need to install all dependencies (if you haven't already):
 
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 If you use ViralConsensus in your work, please cite:
 
 > Moshiri N (2023). "ViralConsensus: A fast and memory-efficient tool for calling viral consensus genome sequences directly from read alignment data." *Bioinformatics*. btad317. [doi:10.1093/bioinformatics/btad317](https://doi.org/10.1093/bioinformatics/btad317)
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+If you use the ViralConsensus web application (rather than the command-line tool), please *also* cite:
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+> Ji D, Aboukhalil R, Moshiri N (2023). "ViralWasm: a client-side user-friendly web application suite for viral genomics." *Bioinformatics*. btae018. [doi:10.1093/bioinformatics/btae018](https://doi.org/10.1093/bioinformatics/btae018)