- Methodology article
- Open Access
- Published:

# A dictionary based informational genome analysis

*BMC Genomics*
**volume 13**, Article number: 485 (2012)

## Abstract

### Background

In the post-genomic era several methods of computational genomics are emerging to understand how the whole information is structured within genomes. Literature of last five years accounts for several alignment-free methods, arisen as alternative metrics for dissimilarity of biological sequences. Among the others, recent approaches are based on empirical frequencies of DNA *k*-mers in whole genomes.

### Results

Any set of words (factors) occurring in a genome provides a *genomic dictionary*. About sixty genomes were analyzed by means of *informational indexes* based on genomic dictionaries, where a systemic view replaces a local sequence analysis. A software prototype applying a methodology here outlined carried out some computations on genomic data. We computed informational indexes, built the genomic dictionaries with different sizes, along with frequency distributions. The software performed three main tasks: computation of informational indexes, storage of these in a database, index analysis and visualization. The validation was done by investigating genomes of various organisms. A systematic analysis of genomic repeats of several lengths, which is of vivid interest in biology (for example to compute excessively represented functional sequences, such as promoters), was discussed, and suggested a method to define synthetic genetic networks.

### Conclusions

We introduced a methodology based on dictionaries, and an efficient motif-finding software application for comparative genomics. This approach could be extended along many investigation lines, namely exported in other contexts of computational genomics, as a basis for discrimination of genomic pathologies.

## Background

Genomes are sequences of nucleotides from hundreds to billions of base pairs long. As sequences of symbols they determine dictionaries, that is, formal languages constituted by words occurring in them. They encode the language of life, as dictating the functioning of all the organisms we consider living beings. A main open problem in science is to find a key to understand such an encrypted language, which more or less directly affects the structure and the interaction of all the cellular and multicellular components [1]. It is like having at hand a book, the language of which has still to be deciphered [2, 3]. Namely, the international long-term project ENCODE [4] is searching for encyclopedias, lexicons, catalogs, of DNA biochemically annotated elements in human genome.

Working on genomic dictionaries requires the elaboration of enormous moles of data. As an example, the dictionary of all the substrings of length 18 occurring in *Drosophila melanogaster*’s genome has more than 116 millions of words, which require, only to be stored, non-trivial implementations of *ad hoc* procedures. To the best of our knowledge, exhaustive studies on collections of *k*-mers were carried out for values of *k* which do not exceed 13 (see for example [5–8]).

The starting point of our analysis was the computation of all *k*-mers, with *k* = 6,12,18, of given genomes, listed in Table 1. Some properties of such specific dictionaries and their compared statistics guided our research along lines of development which were in part already present in the literature [9, 10], and in part took us towards new topics, which emerged just from the empirical evidence of computed data. An interesting concept in this context is that of *hapax* (a Greek term, meaning “once”, coming from philology, where it is used for denoting a “word said once”). In manuscripts these words are relevant for authorship attribution, in genomes they seem to play essential roles in the genome organization as opposed to *repeat* strings, which instead occur more than once.

In Table 1 a list is reported of twelve (out of the sixty we have investigated) genomic sequences, to which we applied the methodology described below. They correspond to genomes of well known organisms, constituting biological models, of relevance in various kinds of genomic analysis. The sequences were downloaded from public websites as FASTA files, and processed by a dedicated Java software that we developed.

In the following basic terminology for genomic dictionaries and multisets, and genomic profiles/distributions, is introduced, along with a simple example focused on a specific DNA sequence. Results are reported in terms of both an analysis of dictionaries of *k*-long hapaxes and repeats, together with the introduction of three related dictionary-based informational indexes, and the definition of *k*-repeat sharing gene networks. Section Discussion is then developed around a phase-transition observed in *k*-dictionaries from *k* = 12 to *k* = 18, and around the structure of genomic information which emerges when dictionary cardinality trends and multplicity-comultiplicity distributions are compared with those of randomly permuted sequences. A description of the software suite developed to perform all our computations is finally presented in section Methods.

### Basic notations

Let us denote by Γ the **genomic alphabet** of four symbols (characters, or letters, associated to nucleotides): Γ={*A*,*T*,*C*,*G*} (then Γ^{⋆}, as usual, denotes the set of all possible words over Γ).

A genome *G* is representable by a sequence over Γ, that is, a table assigning a symbol of Γto each position (from 1 to the length of *G*). Symbols are written in a linear order, from left to right, according to the standard writing system of west languages, and to the chemical orientation 5^{′}−3^{′} of DNA molecules. By associating to each symbol of Γthe set of positions where it occurs, *G* may be equivalently identified by four sets of numbers.

All factors (fragments) of a genome *G* are collected in the set *D*(*G*), while we call **k**-**genomic dictionary of** ** G** (for some

*k*≤ |

*G*|), denoted by

*D*

_{ k }(

*G*), the set of all the

*k*-long substrings of genome

*G*. The

**k**-

**genomic table**

*T*

_{ k }(

*G*), which mathematically corresponds to a

*multiset*, is defined by equipping the words of

*D*

_{ k }(

*G*) with their

**multiplicities**, that is, the number of their respective occurrences in

*G*. Let

*α*(

*G*) denote the multiplicity of

*α*and

*po*

*s*

_{ G }(

*α*) gives the set of positions of

*α*in a genome

*G*(that is, the positions where the first symbol of

*α*is placed). Of course, it holds

*α*(

*G*) = |

*po*

*s*

_{ G }(

*α*)|. Hence, the table

*T*

_{ k }(

*G*) may be represented by an association of strings to their corresponding multiplicities:

*α*↦

*α*(

*G*), with

*α*∈

*D*

_{ k }(

*G*)

*.*The sum of all the multiplicities of elements in

*D*

_{ k }(

*G*) is called the

*size*of

*T*

_{ k }(

*G*), denoted by |

*T*

_{ k }(

*G*)|, with the same sign for string length and for set cardinality (but the context of use should avoid any confusion). It is easy to realize that:

Word distribution in a genome may be represented along a graphical profile, which measures the number of *k*-words having a given number of occurrences. Words having the same multiplicity in a *k*-genomic table *T*_{
k
}(*G*) can be grouped and their number is called **comultiplicity**. As an instance, for the sequence *ATTAGGATCTTAAT*, we have: six 2-words occurring once (i.e., AA, AG, TC, CT, GA, GG), two words occurring twice (i.e., TA, TT), one word (i.e., AT) occurring 3 times, and seven 2-words which do not occur at all.

If we report 2-words multiplicities on the *x*-axis and their number (comultiplicity) on the *y*-axis, we obtain the chart in Figure 1a. We call such curves **multiplicity-comultiplicity** **k** **-distribution** (see Figure 2) of a genome. This kind of charts [5] represents a recent approach in genome analysis, opening new investigation lines about the internal logic underlying genome organizations. The same information may be graphically reported as a rank-multiplicity Zipf map (usually employed to study word frequencies in natural languages [11]). As one may notice by looking at Figure 2, both the middle and final inclination of Zipf’s curves is different for four of our organisms, accounting for the multiplicity range in which we have a major density of strings. In all cases, we have few units with maximal multiplicity, indeed Zipf curves initially slope down steeply.

Several other nice representations of genomic frequencies may be found in the literature, for example by means of images (in [7], distance between images results in a measure of phylogenetic proximity, especially to distinguish eukaryotes from prokaryotes).

## Results

Two important types of factors of genomes are hapaxes and repeats. A **hapax** of a genome *G* is a factor *α* of *G* such that *α*(*G*) = 1. A **repeat** of *G* is a factor *α* of *G* such that *α*(*G*) > 1. Two or more contiguous occurrences of one repeat form a sequence technically called *tandem repeat*, if the repeated sequence is shorter than 10 nucleotides, one has a *minisatellite* or *short tandem repeat*. They describe patterns helpful to determine individual’s inherited traits, namely to determine parentage or genealogical information.

Back to the dictionaries, the set *H*(*G*) of hapaxes of *G* and the set *R*(*G*) of repeats of *G* of course constitute a bipartition of *D*(*G*) (at least one element of Γ is a repeat and *G* is a hapax, therefore *H*(*G*) and *R*(*G*) are nonempty, also disjoint sets, such that their union is *D*(*G*)). We set

where ∩ is the set-theoretic intersection.

Therefore, given a genome *G* of length *n*, for any *k* ≤ *n* we can read it according to the bi-partition of its *k*-genomic dictionaries *H*_{
k
}(*G*) and *R*_{
k
}(*G*). Size variations of *k*-genomic, *k*-hapax and *k*-repeat dictionaries, for *k* = 1,…,18, are analyzed in the following (see Tables 2, 3, 4 for numerical data), while the size of “forbidden dictionaries” (those composed by “non-appearing” *k*-words, said also “nullomers” [12]), for given genomes, is of course exponentially increasing with *k*.

According to data reported in Table 2, in the first three genomes of the list, |*D*_{6}(*G*)| slightly decreases and repetitiveness slightly increases for longer genomes. When the analyzed genomes length exceeds about 1,800,000 base pairs, the decomposition of *D*_{6} in hapaxes and repeats keeps the identical respective cardinalities. All the 6-genomic dictionaries are composed by only repeat words (i.e., they do not contain any hapax).

In Table 3, the number of hapax words |*H*_{12} (*G*)| appears not related to the length of genome G, and neither to the cardinality of *D*_{12}(*G*); while the ratio of 12-hapaxes over 12-repeats *H* *R*_{12} appears roughly decreasing with the genome length. This is due to the fact that 12-repeat words constitute a considerable portion of 12-genomic dictionary, actually a percentage (called *R* *D*_{12}) which increases with the genome length (from 11% to 90%). The average 12-factors repeatability index, in the last column, accounts for the average repeatability of 12-repeats in all the genomes.

In Table 4, cardinality of *D*_{18}and *H*_{18}increase with the genome length, as expected. As a notable result though, we can see that the 18-repeat-factor ratio *R* *D*_{18} is firmly fixed (over all the genomes) on a very small portion of the 18-genomic dictionary, mostly ranging from 0.01 to 0.07 (and always less than 1%), independently on the genome length. The 18-hapax-repeat ratio *H* *R*_{18} does not show a regular behavior with respect to the length, but its values are considerably greater for longer words (according to the data, for *k* = 12 and *k* = 18). The average 18-factor repeatability index does not exhibit the regularity of the average 12-factor repeatability with respect to the genome length, it even shows an exceptionally high value for the chromosome 19 of *H. sapiens*.

It is easy to see that any genomic factor containing a hapax as a substring is an hapax as well. Hence an hapax within the genome may be elongated (by keeping its property to be an hapax) up to reach the genome itself, which is of course an hapax. It is then interesting to evaluate, for each genome *G*: *i)* how |*H*_{
k
}(*G*)| varies with *k* (see http://www.cbmc.it/external/Infogenomics3), *ii)* the *k*-hapax positions (that is, how densely hapax words fall in the genetic regions), and *iii)* the shortest length of an hapax. Also, a *k*-similarity between genomes *G* and *G*^{′} could be measured by |*H*_{
k
}(*G*)∩*H*_{
k
}(*G*^{′})| (we have some work in progress on the computation of dictionary intersections).

The concepts of hapax and repeat provide a great number of related notions which permit to define important aspects in the analysis of real genomes. In following sections we will discuss numerical data, reported in tables, diagrams, and figures, which include the measure of the ratio between |*H*_{
k
}(*G*)| and |*R*_{
k
}(*G*)| as a function of *k* (that is, how the number of hapax words of a given length increases or decreases with respect to the number of repeats of that length). We observed a sort of *transition phase* effect in the passage from *D*_{12}(*G*) to *D*_{18}(*G*), in almost all genomes of Table 1, where a clear inversion appears in the ratio hapax-cardinality/repeat-cardinality.

### Dictionary based indexes

For a genome *G* we may define **k**-**lexicality**, that is, the ratio *L*_{
k
}(*G*) = |*D*_{
k
}(*G*)|/|*T*_{
k
}(*G*)|, which expresses the percentage of distinct *k*-factors of *G* with respect to the all the *k*-factors present in G (in Tables 2, 3, 4, it is clear that the *k*-lexicality increases with the word length *k*, and does not exhibit any regularity with the genome length). Of course, the inverse of this ratio provides an average repeatability of *k*-factors in *G*.

A more refined measure for the **average** **k**-**factors repeatability** in *G* may be now given as:

where *k*-hapaxes have been excluded by both the *k*-genomic multiset and the *k*-genomic dictionary (the symbol ∖ represents the set-theoretic difference). Index *A* *R*_{
k
}(*G*) counts the proper (average) repeatability of *k*-repeats in genome G (see Tables 3 and 4 for computed numerical values).

Finally, *maximal repeats* of a genome *G* are substrings occurring at least twice and having maximal length. Some numerical indexes related to this concept are *i)* the maximal repeat length *MR*(*G*), *ii)* the number of different maximal repeat sequences, and *iii)* the number of times each maximal subsequence is repeated (see Table 5).

All genomes turned out to have only one repeat having maximal length (and multiplicity 2), and the distance of the two positions (in proportion to the genome length) is reported in Table 5. They are in most cases relatively very close. Although for *k* = 6,12,18, |*R*_{
k
}| increases with the genome length *n*, there is no apparent correlation between *n* and the MR index (in all cases |*R*_{
MR
}| = 2).

Any substring of a repeat word is still a repeat, with an own multiplicity along the genome, and inside the repeat word itself. A further index is thus defined over genomes G, called *MR*(*G*) (**maximal repeat length**), as the maximal length of words Γsuch that *γ*(*G*) > 1. An algorithmic way to find it (for our genomes) starts from repeats out of *D*_{18}(*G*) (that are less than three a half millions) and checks how much they may be elongated on the genome by keeping their status of repeat words. Data related to the MR index computed over our genomes are reported in Table 5, where the only MR-long repeat of each genome exhibits a non-trivial structure (that is, different than polymers with a same nucleotide or similar patterns), and complex repeats are obtained for many lengths.

The importance of word repeatability is crucial in understanding the information content of texts. A genome analysis in terms of (shortest) hapaxes and (maximal) repeats, providing their relative distribution within the genome, highlights the associative nature of DNA as a container of information [13]. Localization (see Figure 1b) and frequency (see Figure 2) of DNA fragments of specific length is indeed crucial in understanding the information organization of genomes [14].

### Repeat-sharing gene networks

Once we discovered that the percentage of repeats in dictionaries is “low” (and decreasing with *k*), we focused on studying the positions of 18-repeats along the genome, in order to check if they are more densely present in encoding regions or non-coding ones. This investigation allowed us to design a synthetic gene network in the following way: nodes are genes, and they are connected by an edge if they have at least one common repeat (that is, there exists a repeat which is a proper factor common to the two genes). An interest for this kind of diagram (see examples in Figures 3 and 4) finds a motivation in the hypothetic communication between genes due to competitions for short endogenous RNA sequences (around 20 bases long) proposed in [15].

We have work in progress to investigate these *k*-parametrized labeled gene networks by standard methods of graph theory and network analysis. Gene nodes with higher degrees turned out to be actually involved in important long genetic pathways, and for specific values of *k*, between 16 and 18, drastic changes may be observed in the network conformation, while emerging several clusters of genes. However, this is out of the scope of this work, even if it will be a natural extension of it.

## Discussion

In this session we would like to specifically discuss the computational results reported in all the tables, and the importance of reading a genome by its mutliplicity-comultiplicity *k*-distribution. In both cases internal structural properties of genomes emerge which highlight regularity indicators, based on the number and distribution of repeats.

For all our genomes of Table 1, listed according to an increasing genome length order, we report in Tables 2, 3, and 4 numerical data related to the computation of *D*_{
k
}(*G*),*H*_{
k
}(*G*),*R*_{
k
}(*G*) for *k* = 6, 12, and 18, respectively^{a}.

A peculiar phenomenon regarding hapax statistical distribution may be observed passing from the 12- to the 18-genomic dictionary (see Tables 3 and 4). For all the genomes, by enlarging the *k* value, the number of hapax increases, even relatively to the number of repeats (roughly speaking, “most of the 12-words are repeats while most of 18-words are hapax”). Indeed, by computing $H{R}_{k}=\frac{\left|{H}_{k}\right|}{\left|{R}_{k}\right|}$ for *k* = 12,18, we see that repeatability generally increases with genome length for *k* = 6,12, while this regularity disappears for *k* = 18.

More interestingly, the (relative) amount of hapaxes increases by some orders of magnitude with *k* passing from 12 to 18. Based on this observation coming from computational experiments, one could suppose that by increasing the word size, genomic dictionaries composed of only hapaxes may be computed (which would have been good news for genome reconstruction algorithms [16, 17]). This intuition though has been invalidated by further computations (see Table 2). In fact, repeats having length of several thousands have been found within each of our genomes (see for example Figure 5, and the website http://www.cbmc.it/external/Infogenomics3), and 12→18 represents a sort of phase transition from scarce to abundant hapax/repeat distribution. This phenomenon would surely deserve a more detailed and generalized analysis.

### Random vs real genomes

We have carried out a systematic study of repeat distribution, of real and randomly permuted genomes (that are, random sequences having the same nucleotide frequencies of the original genome), in order to get new information on the structure of such relevant motifs [14].

We produced some diagrams showing how the number of genomic, hapax, and repeat words of a given length varies with respect to the length (see website http://www.cbmc.it/external/Infogenomics3), and a common remarkable finding is the similar shapes of the curves, where the transition aforementioned occurs. Cardinality trends of sets *D*_{
k
}(*G*) (dictionary words), *R*_{
k
}(*G*) (repeat words), and *H*_{
k
}(*G*) (hapax words), for *k* = 1,…,18 are compared for genomes and their random permutations, and specifically for Human chromosome, a greater difference between random and non-random situation may be clearly observed (see Figure 6).

If we compare the dictionaries of the genome with those of its random permutation (in Figure 6, respectively, big blue versus small red dots), we find quite similar curves. However, even when diagrams follow the same general trends, specific characters of these curves correspond to features which are typical of the single genomes [18]. In general, random values are always considerably greater than non-random values, for both hapax and whole dictionaries, while the opposite appears for repeats, before and after the distribution peaks.

All the data were confirmed along with several random permutations. However, apart of the comparison with permuted sequences, we would like to observe the shape of |*R*_{
k
}| in itself. Only in a limited range of values for *k*, *R*_{
k
}has a significant size, and such a range is [7, 17] for all the analyzed genomes, with a pick around the value *k*=10, while both shifting towards the values 11, 12 for the pick, with the increasing of genome length.

Multiplicity-comultiplicity charts have been computed for all the genomes as well, by means of an application of the software described in the Methods section. displays some of them for 6-words of four organisms: *Escherichia coli*, *Saccharomyces cervisiae*, *Drosophila melanogaster* and *Homo sapiens (chromosome 19)*. Blue bars are related to real genome sequences and red bars concern random permutations of the same sequences. At a first glance, in real genome distributions (blue bars) we notice a common trend, very similar to a Poisson distribution, with specific peculiarities which characterize each genome. On the other hand, random permutations of genomic sequences have multimodal distributions which depend on base frequencies.

We observe that the multplicity-comultiplicity distribution of *Escherichia coli* has multiplicities (*x*-axis) between about 0 and about 5,400, whereas *Drosophila melanogaster* has multiplicities between about 5,000 and about 330,000. On the other hand, the maximum comultiplicity is 8 for *Escherichia coli*, and is 3 for *Drosophila melanogaster* (in Figure 7, see the *y*-axis of the first and the third charts). These parameters are very different even if the “shape” of the genomic sequences in the two charts is quite similar. In order to perform a comprehensive analysis of multplicity-comultiplicity distribution we have dealt with them as probability distributions, and we have computed about 25 statistical indexes which characterize them, such as, maximum, minimum and mean multiplicity, maximum, minimum and mean comultiplicity, standard deviation, kurtosis, skewness, mode, entropy, etc. In [18] these indexes have been successfully employed to classify genomes according to their organism kingdom.

As a conclusion, in Figure 7 we would like to point out that in cases of random permutations of genomes, multimodal shapes may be observed, which depend on the base frequencies of genomes. However, the apparently more ordered concentrations of word multiplicities, around the modes, can be explained by considering that frequencies allow us to classify (and count) words corresponding to the same multiset (Parikh vector equivalent). Consequently, due to the random effect, being the words with the same multiset equally probable, they concentrate around the multiplicity associated to this probability. These distribution differences between randomly permuted genomes and real genomes is another measure of the information content that genomes have with respect to casual sequences.

## Conclusions

Bipartition of a genomic dictionary in hapax and repeat words emphasizes the roots of precise string categories which are related to the functional organization of genomes. The set of 18-repeats in our genomes has a digital size which is a couple of orders smaller than the whole genome, and it seems to have a role of “lexical” coding, that is, a semantics external to the genome. Other elements, with a notably bigger digital size, seem to have a role of addressing, delimiting, coordinating, just like position-identification tags.

The definition, computation, and analysis of well characterized dictionary based genomic indexes have pointed out some phenomena of genomic regularity and specificity. They can highlight our knowledge about the internal logic of genome structure and organization, as well as about evolutional and functional attributes of genomes (as in [18], specifically devoted to genome clustering).

### Future work

There are several lines of development that our research is intended to pursue. We are already working on some of these, mainly focused on the study of intersections among genomic dictionaries. It would be interesting to check the relationship between words recurrent in dictionary intersections and those which are known to be conserved along the evolutive lineages. Another research line concerns the inter-genomic character of hapaxes and repeats. The question is about which hapaxes (respectively repeats) of a given genome occur in other genomes of a certain class by keeping their status of hapax (resp. repeat) when compared to the new context of words.

Finally, we conclude with a fundamental question which points out a novel perspective related to the approach developed in the paper: what is the essence of a genome? For genome functions, two aspects are essential: the presence of some factors and their relative positions. Discovering which factors are essential, the classes related to their roles, and the mechanisms for expressing their relative positions, could provide essential properties of genomes, even without a detailed knowledge of their whole sequence. The approach outlined in this paper could be considered as a first step in the exploration of this perspective.

## Methods

The genome analysis described so far requires a rigorous protocol and a sophisticated technological infrastructure in order to be performed systematically. Dictionaries, tables, distributions and related indexes, described so far, need a lot of computational resources to be calculated, and advanced data exploration and visualization tools to be analyzed. We have developed a process (and a related software suite), shown in Figure 8, for informational index generation and analysis. It involves three main phases: *(i)* acquisition of genomic sequences from public databases, *(ii)* computation of informational indexes, which are subsequently stored in a database, *(iii)* visualization, exploration and quantitative analysis of these informational indexes.

Sequences were downloaded as FASTA files from *NCBI genome database*[19], UCSC Genome Bioinformatics website [20] and EMBL-EBI website [21], and they were stored, with their accession numbers and identification data, on our server. About sixty sequences have been analyzed so far, corresponding to genomes of well known organisms, often constituting biological models, of remarkable relevance in the genomic analysis. All classes of Archea, Bacteria, and Eucaryotes^{b} are represented.

The software employed to process genomic sequences and to compute informational indexes is a sophisticated service oriented architecture based on Java web services. The Java EE application model guarantees the scalability, accessibility, and manageability needed by our application. Each index is computed by a specific web service which receives as an input a genomic sequence with some additional parameters, and stores the results in a *MySQL* database, representing the data warehouse of our infrastructure.

Optimized data structures and algorithms were required to perform index computation since huge amount of data had to be processed. The entire application is hosted by a high performance server having 16 processors and 24GB of RAM. Our index database currently contains about 100GB of data, consisting of 300 millions of records. The amount of information generated by web services is sometimes very large (e.g., a 12-genomic dictionary *D*_{12}(*G*) could have up to 4^{12} ≈ 16 millions of words) and the storage of this information in databases could require quite a lot of time and specific database setting. The advantage to use web services to compute informational indexes is that they can be called by many kinds of application clients. In this section we have described only a *Java* application client, but web clients or non-Java clients (e.g., *Microsoft.Net* or *Matlab* clients) could be employed as well. Web services guarantee a great interoperability and extensibility to our application.

The visualization and exploration of such an enormous dataset requires specific tools as well. We have adopted a data access solution, called Qlik^{®}View [22], coming from the world of *Business Intelligence* (where sophisticated elaborations of huge moles of economic and financial data are performed). This tool enables an interactive exploration of large and complex datasets by means of a patented *in-memory associative technology*.

Figure 9 shows a screenshot of the Qlik^{®}View application, which has two main sections. A *navigation menu*, on the left, by which the user can select genome sequences, organism kingdoms and dictionary parameters. A *central area* containing visualization elements of genomic indexes, such as tables, charts, lists of words, and diagrams.

Tabs differ only in the central area, where informational indexes are displayed by means of several kinds of graphical objects provided by Qlik^{®}View. This way to visualize and browse the information is very powerful and enables the user to achieve a deep insight into the genomes. The following list summarizes the functionalities developed so far which contained in the tabs: genome basic indexes (genome identificators, base frequencies, gc-content, etc.); *k*-Dictionaries and Multiplicity-Comultiplicity distributions; normalizations of indexes at the previous item; statistical parameters (e.g., mean, standard deviation, mode, *k*-empirical entropy, etc.) related to Multiplicity-Comultiplicity distributions; dictionary intersections; maximal repeat lengths; dictionary size trends.

## Endnotes

^{a}When analyzing downloaded genomes, in some cases we have found a number *num* of *unavoidable words*, defined as those containing IUPAC (variable) symbols, which can assume one of the values A, T, C, G (see http://www.mun.ca/biochem/courses/3107/sym-bols.-html). When they are present in a genome, such as the case of Haemophilus Influenzae, they are eliminated from the computation of all words in the genome, then the *k*-genomic dictionary is built up not from *n*−*k* + 1 genomic *k*-long words, but from the *n*−*k*−*num* + 1 regular words. Specifically, as value of *num* we have found: for *H. influenzae*’s 6/12/18-genomic dictionary, respectively 646, 1,271, 1,877; for *D. melanogaster*’s 6/12/18-genomic dictionary, respectively 1,225,656, 1,226,400, 1,227,144; for *H. sapiens*’ 6/12/18-genomic dictionary, respectively 1,171,155, 1,173,045, 1,174,935.

^{b}A most detailed description of these genomes may be found in: http://use-rs.rcn.com/jkimball.ma.ultranet/BiologyPages/G/Genome-Sizes.html.

## Author’s contributions

This paper is a first step towards a project, called Infogenomics, conceived and designed by the last author VM, who defined an initial kernel of informational indexes, to be investigated and compared on specific genomes. A sophisticated service oriented architecture (SOA) based on Java web services and a Qlik^{®}View application, has been developed by the first author AC, in order to make possible the high amount of computations necessary for the informational analysis of genomes. All the authors discussed and agreed on the interpretation of experimental results, with a main role of GF in the preparation of the paper. All authors read and approved the final manuscript.

## References

- 1.
Gibson DG, et al: Creation of a Bacterial Cell Controlled by a Chemically Synthesized Genome. Science. 2010, 329 (5987): 52-56. 10.1126/science.1190719.

- 2.
Gibson G, Muse SV: A Primer of Genome Science. 2009, Sinauer Associates Inc

- 3.
Percus JK: Mathematics of Genome Analysis. 2007, Cambridge Studies in Mathematical Biology: Cambridge University Press

- 4.
The ENCODE Project consortium: ENCODE. Nature. 2012, 489 (7414): 45-113. 10.1038/489045a.

- 5.
Chor B, Horn D, Goldman N, Levy Y, Massingham T: Genomic DNA k-mer spectra: models and modalities. Genome Biol. 2009, 10: R108-10.1186/gb-2009-10-10-r108.

- 6.
Zhou F, Olman V, Xu Y: Barcodes for genomes and applications. BMC Bioinf. 2008, 9: 546-10.1186/1471-2105-9-546.

- 7.
Deschavanne PJ, Giron A, Vilain J, Fagot G: Genomic Signature: Characterization and Classification of Species Assessed by Chaos Game Representation of Sequences. Mol Biol Evol. 1999, 16 (10): 1391-1399. 10.1093/oxfordjournals.molbev.a026048.

- 8.
Hao B, Qi J: Prokaryote phylogeny without sequence alignment: from avoidance signature to composition distance. J Bioinf and Comput Biol. 2004, 2: 1-19. 10.1142/S0219720004000442.

- 9.
Fofanov Y, Luo Y, Katili C, Wang J, Belosludtsev Y, Powdrill T, Belapurkar C, Fofanov V, Li TB, Chumakov S, Pettitt B: How independent are the appearances of n-mers in different genomes?. Bioinformatics. 2008, 20 (15): 2421-2428.

- 10.
Vinga S, Almeida: Alignment-free sequence comparison - a review. Bioinformatics. 2003, 19 (4): 513-523. 10.1093/bioinformatics/btg005.

- 11.
Mantegna RN, Buldyrev S, Godberger A, Havlin S, Peng C, Simons M, Stanley H: Linguistic Features of Noncoding DNA Sequences. Phys Rev Lett. 1994, 73 (23): 3169-3172. 10.1103/PhysRevLett.73.3169.

- 12.
Hampikian G, Andersen T: Absent sequences: nullomers and primes. Pac Symp Biocomputing. 2007, 12: 355-366.

- 13.
Haubold B, Pierstorff N, Möller F, Wiehe T: Genome comparison without alignment using shortest unique substrings. BCM Bioinf. 2005, 6: 123-10.1186/1471-2105-6-123.

- 14.
Ichinose N, Yada T, Gotoh O: Large-scale motif discovery using DNA Gray code and equiprobable oligomers. Bioinformatics. 2012, 28: 25-31. 10.1093/bioinformatics/btr606.

- 15.
Tai Y, et al: Coding-Independent Regulation of the Tumor Suppressor PTEN by Competing Endogenous mRNAs. Cell. 2011, 147: 344-357. 10.1016/j.cell.2011.09.029.

- 16.
Fici G, Mignosi F, Restivo A, Sciortino M: Word assembly through minimal forbidden words. Theor Comput Sci. 2006, 359: 214-230. 10.1016/j.tcs.2006.03.006.

- 17.
Cicalese F, Erdös P, Lipták Z: Efficient reconstruction of RC-equivalent strings. IWOCA 2010 - LNCS 6460. Edited by: Iliopoulos C, Smyth WF . 2011, 349-362.

- 18.
Castellini A, Manca V, Compri S, Tosadori G, Bicego M: Genome classification by dictionary-based indexes. Poster, presented at the Int. Conf. on Pattern Recognition in Bioinformatics (PRIB2011). 2011, TU Delft

- 19.
NCBI Genome database. [http://www.ncbi.nlm.nih.gov/sites/genome]

- 20.
UCSC Genome Bioinformatics website. [http://hgdownload.cse.ucsc.edu/downloads.html]

- 21.
EMBL-EBI website. [http://www.ebi.ac.uk/genomes/]

- 22.
QlikView website. [http://www.qlikview.com/]

## Acknowledgements

The first author was funded by CBMC (Center for Biomedical Computing), in Verona, Italy, which also provided us with the high-performance server where all the computations were performed.

## Author information

### Affiliations

### Corresponding author

## Additional information

### Competing interests

The authors declare that they have no competing interests.

## Authors’ original submitted files for images

Below are the links to the authors’ original submitted files for images.

## Rights and permissions

## About this article

### Cite this article

Castellini, A., Franco, G. & Manca, V. A dictionary based informational genome analysis.
*BMC Genomics* **13, **485 (2012). https://doi.org/10.1186/1471-2164-13-485

Received:

Accepted:

Published:

### Keywords

- Comparative genomics
- Computational genomics
- Genome clustering
- Information theory
- Sequence analysis