This feature allows for detailed alignment of nucleotide or protein sequences, enabling comparison between multiple sequences to identify regions of similarity, conservation, or variation. Upload your sequences in FASTA or similar formats via the file system, and the platform will generate a clear, interactive visualization of the alignment. This includes gap placement, mismatches, and similarity scores, providing a comprehensive view of how sequences relate to each other. The alignment tool is ideal for tasks such as phylogenetic analysis, identifying conserved domains, or detecting mutations.