Motivation: An unmanageably large amount of data on genome sequences is accumulating, prompting researchers to develop new methods to analyze them. We have devised a novel method designated oligostickiness, a measure roughly proportional to the binding affinity of an oligonucleotide to a DNA of interest, in order to analyze genome sequences as a whole. Results: Fifteen representative genomes such as Bacillus subtilis, Escherichia coli, Saccharomyces cerevisiae, Caenorhabditis elegans, H.

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... and others were analyzed by this method using more than 50 probe dodecanucleotides, offering the following findings: (i) Genome sequences can be specifically featured by way of oligostickiness maps. (ii) Oligostickiness analysis, which is similar to but more informative than (G+C) content or repetitive sequence analysis, can reveal intra-genomic structures such as mosaic structures (E. coli and B. subtilis) and highly sticky/non-sticky regions of biological meanings. (iii) Some probe oligonucleotides such as dC 12 and dT 12 can be used for classifying genomes, clearly discriminating prokaryotes and eukaryotes. (iv) Based on global oligostickiness, which is the average value of the local oligostickinesses, the features of a genome could be visualized in spider web mode. The pattern of a spider web as well as a set of oligostickiness maps is highly characteristic to each genome or chromosome. Thus, we called it as chromosome texture, leading to a finding that all the chromosomes contained in a cell, so far investigated, have a common texture. Availability: Oligostickinesses maps used in this work are available at