Changes in version 0.1.0 First release of the rewritten Clusnalyst, as an R package with the app inside. Compared with the 2022 app - Reads 0/1 band tables, SNP genotypes as letters, 0/1/2, VCF or HapMap, measured and categorical traits, and DNA or protein FASTA. The data type and table layout are detected and can be overridden. - Quality check step with filters for missing data, minor allele frequency and markers that do not vary. Sequences are aligned with ClustalOmega, ClustalW or MUSCLE. - New distances: allele sharing (IBS), modified Rogers, Euclidean, Manhattan, Gower, and K80, JC69, TN93 and p-distance for sequences. - New tree methods: WPGMA, Ward, BIONJ, and NJ rooted on an outgroup. A cophenetic correlation table compares them. - Number of groups from silhouette width, the within-group sum of squares and the gap statistic. Mantel tests against a second matrix or against numeric sample information such as location. - PCoA and PCA, and groups from cutting the tree, PAM or k-means. - Interactive trees and plots, sample information on hover, light and dark themes, a guided tour. - Downloads: PNG, SVG and PDF for every figure, CSV and Excel tables, Newick trees, an HTML report, an R script that repeats the analysis, and a session file. Fixed from the 2022 app - The "Single" and "Complete" options ran Ward.D and Ward.D2. - Bootstrap support came from resampling the columns of the distance matrix. It now resamples markers (or alignment sites) and rebuilds the distances, as in Felsenstein (1985). - Data were kept in global variables, so people using the hosted app at the same time could overwrite each other's results. Each session now has its own state. - Choosing "already aligned" for a FASTA file crashed, and DNA could not be read. - Removing monomorphic markers failed when there were none, and letter genotypes with missing calls were coded wrongly. - Silhouette analysis failed for neighbour-joining trees.