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  <front>
    <journal-meta />
    <article-meta>
      <title-group>
        <article-title>Description, Characteristic And Algorithm For Creation Of A Dictionary Of Cell Types And Tissues In The Gtrd Database1</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <string-name>Michael A Kulyashov</string-name>
          <email>m.kulyashov@developmentontheedge.com</email>
          <xref ref-type="aff" rid="aff0">0</xref>
          <xref ref-type="aff" rid="aff1">1</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Sergei К. Kolmykov</string-name>
          <xref ref-type="aff" rid="aff0">0</xref>
          <xref ref-type="aff" rid="aff1">1</xref>
          <xref ref-type="aff" rid="aff2">2</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Ivan S. Evshin</string-name>
          <xref ref-type="aff" rid="aff0">0</xref>
          <xref ref-type="aff" rid="aff1">1</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Fedor A. Kolpakov</string-name>
          <xref ref-type="aff" rid="aff0">0</xref>
          <xref ref-type="aff" rid="aff1">1</xref>
        </contrib>
        <aff id="aff0">
          <label>0</label>
          <institution>Biosoft.ru</institution>
          ,
          <addr-line>Novosibirsk</addr-line>
          ,
          <country country="RU">Russia</country>
        </aff>
        <aff id="aff1">
          <label>1</label>
          <institution>Institute of Computational Technologies SB RAS</institution>
          ,
          <addr-line>Novosibirsk</addr-line>
          ,
          <country country="RU">Russia</country>
        </aff>
        <aff id="aff2">
          <label>2</label>
          <institution>Institute of Cytology and Genetics SB RAS</institution>
          ,
          <addr-line>Novosibirsk</addr-line>
          ,
          <country country="RU">Russia</country>
        </aff>
      </contrib-group>
      <fpage>13</fpage>
      <lpage>18</lpage>
      <abstract>
        <p>The GTRD database (http://gtrd.biouml.org) contains information on transcription factor binding sites and open chromatin. The cell types and tissues presented in the GTRD: 1) were arranged in a single dictionary (3954 entries); 2) were divided into 90 unique clusters; 3) 3225 records were compared with main databases of cell types; 4) were used to match experiments with the databases of transcription regulation: 588 for FANTOM 5, 5962 for ENCODE and 21720 for GTEx.</p>
      </abstract>
      <kwd-group>
        <kwd>GTRD</kwd>
        <kwd>database structure</kwd>
        <kwd>dictionary of cell types and tissues</kwd>
        <kwd>cell type onthology</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
    <sec id="sec-1">
      <title>Introduction</title>
      <p>
        The GTRD database (Gene Transcription Factors Database, http://gtrd.biouml.org) contains information on
transcription factor binding sites and open chromatin sites that have been experimentally identified in various cell types
and tissues using high-performance ChIP-seq and DNase-seq methods respectively [
        <xref ref-type="bibr" rid="ref1">1</xref>
        ]. GTRD currently contains the
largest number of uniformly processed experiments of the corresponding types in the world
(http://wiki.biouml.org/index.php/GTRD_comparison).
      </p>
      <p>A separate ChIP-seq experiment allows all binding sites for a single transcription factor to be identified for a single
cell type (with or without treatment) or a tissue fragment excreted from the body. A separate DNase-seq experiment
will allow to identify all sections of open chromatin also only for a single cell type (with or without treatment) or a
tissue fragment. Therefore, to integrate data on a given cell type or tissue, it is necessary to maintain a dictionary of cell
types and tissues.</p>
      <p>
        To understand the regulation of transcription the important step is integration of GTRD with the main specialized
transcription regulation databases, the main of which are:
- ENCODE [
        <xref ref-type="bibr" rid="ref2">2</xref>
        ] is a project whose purpose is to analyze the functional elements of the genome;
- FANTOM5 [
        <xref ref-type="bibr" rid="ref3">3</xref>
        ] is a project aimed at studying the regulation of transcription in various cell types and tissues of a
human and mouse;
- GTEx [
        <xref ref-type="bibr" rid="ref4">4</xref>
        ] is a project aimed at studying tissue-specific expression and mechanisms of gene regulation of human.
      </p>
      <p>At the stage of developing these databases, the issue of systematization of cell types and lines was also raised. To
solve this problem, specialized databases are used to compare cell types and tissues (Table 1).</p>
      <sec id="sec-1-1">
        <title>Database</title>
        <p>name</p>
        <p>EFO
(Experimenta</p>
        <p>
          l factor
ontology)[
          <xref ref-type="bibr" rid="ref5">5</xref>
          ]
        </p>
        <p>Database description</p>
      </sec>
      <sec id="sec-1-2">
        <title>An ontology that describes various cellular states, experimental conditions, and developmental stages.</title>
      </sec>
      <sec id="sec-1-3">
        <title>Prefix</title>
        <p>EFO</p>
      </sec>
      <sec id="sec-1-4">
        <title>Databases which uses this ontology database</title>
      </sec>
      <sec id="sec-1-5">
        <title>ENCODE,</title>
      </sec>
      <sec id="sec-1-6">
        <title>FANTOM 5,</title>
      </sec>
      <sec id="sec-1-7">
        <title>GTEx</title>
      </sec>
      <sec id="sec-1-8">
        <title>UBERON (UBER anatomy atlas)[6]</title>
      </sec>
      <sec id="sec-1-9">
        <title>Cell ontology[7]</title>
      </sec>
      <sec id="sec-1-10">
        <title>BRENDA tissue ontology[8]</title>
      </sec>
      <sec id="sec-1-11">
        <title>Plant ontology[9]</title>
      </sec>
      <sec id="sec-1-12">
        <title>Cellosaurus</title>
        <p>
          [
          <xref ref-type="bibr" rid="ref10">10</xref>
          ]
        </p>
        <p>Ontology of various anatomical
structures of animals, which is
composed taking into account all
modern ideas about the anatomical
structure, functioning and stages of
development.</p>
        <p>This ontology describes various
types of cells.</p>
      </sec>
      <sec id="sec-1-13">
        <title>In this anthology, a huge amount of</title>
        <p>various data is collected, cell types,
tissues, cell cultures for various
taxonomic groups, such as animals,
plants, fungi, protozoa.</p>
        <p>Ontology with a description of
various anatomical and
morphological structures of plants, as
well as data on the growth and
development of plants.</p>
        <p>A resource that contains a
description of a large number of cell
lines, as well as data on the
relationship of cell lines that are used
in many biomedical studies.</p>
        <p>CL
BTO
PO</p>
      </sec>
      <sec id="sec-1-14">
        <title>ENCODE, FANTOM 5, GTEx</title>
      </sec>
      <sec id="sec-1-15">
        <title>ENCODE, FANTOM 5, GTEx</title>
      </sec>
      <sec id="sec-1-16">
        <title>ENCODE, FANTOM 5, GTEx</title>
      </sec>
      <sec id="sec-1-17">
        <title>CVCL</title>
      </sec>
      <sec id="sec-1-18">
        <title>ENCODE</title>
        <p>2</p>
      </sec>
    </sec>
    <sec id="sec-2">
      <title>Materials and Methods</title>
      <p>To create a dictionary of cell types and tissues and then compare experiments between GTRD and transcription
regulation bases, a plan of work was developed as shown in Figure 1, where each stage of development is numbered.</p>
      <p>For this work, the following principle was used: the original tissue and developmental stage on which cell type or
tissue was extracted. To determine the type of cells and tissues that failed to determine the organ, anatomical or
morphological system in which they are located, was made a separate group “Others”. Data was recorded according to
the principle of “key” - “value”, where the key is the name of the cluster and the value is name of cell type or tissue
from GTRD.</p>
      <sec id="sec-2-1">
        <title>Comparison of cell types and tissues with specialized databases.</title>
        <p>For creation of a dictionary of cell types and tissues the following databases were selected: EFO, Brand Ontology,
UBERON, Cell Ontology, Plant Ontology (Table 1). The comparison of the cell type or tissue was carried out according
to the following principle: the assignment of the most accurate data that would allow all the information to be obtained,
but at the same time they would not give characteristics that contradict this cell type and tissue. This work is done by
using semi-automatic and manual annotation methods:</p>
        <p>
          1) Semi-automatic annotation - for this was developed the program in Python 3.6, which for each cell type and tissue
located in the GTRD performed a search on the databases described in table 1, using the API ontology search service
[
          <xref ref-type="bibr" rid="ref11">11</xref>
          ]. Results that satisfy the above points have been added to the GTRD.
        </p>
        <p>2) manual annotation was carried out for cell types and tissues,for which didn’t find any matches.</p>
        <p>The data obtained are recorded on the principle of “key” - “value”, where the key corresponds to the name of the
cell type or tissue from GTRD, and value is a matched record from specialized databases.
2.3 Comparison of dictionaries of cell types and tissues between GTRD and the transcription regulation
database.</p>
        <p>For this work was developed a program in Python 3.6, which checked for matching entries from the GTRD
dictionary with available transcription regulation databases (ENCODE, FANTOM5, GTEX). After that, the list was
checked for errors.
2.4</p>
      </sec>
      <sec id="sec-2-2">
        <title>Comparison of experiments between GTRD and the transcriptional regulation database.</title>
        <p>Comparison of experiments between GTRD and the transcriptional regulation database. To do this, we used a
program written in Python 3.6, which compares all the experimental data in the database with each cell type and tissue.
Then, on the basis of the comparison obtained earlier, between the dictionaries of cell types and tissues of GRTD and
transcription regulation databases, experiments were compared. After this, list has been checked manually to eliminate
errors and also for each experiments for which the results of automatic annotation didn’t find any matches or which are
comparable only for cluster to which cell type or tissue from experiment belong.
2.5</p>
      </sec>
      <sec id="sec-2-3">
        <title>Creating additional keys to describe the experiments.</title>
        <p>When describing the experimental data in the GTRD, in addition to the cell type or tissues, it is necessary to indicate
conditions, some of which are given in Table 2. These conditions are formed in the form of a key-value set and are
attached to the results of the GTRD experiments.</p>
        <p>Key
Treatment</p>
        <sec id="sec-2-3-1">
          <title>Genotype Sex Age</title>
        </sec>
        <sec id="sec-2-3-2">
          <title>Meaning</title>
          <p>This key describes whether the treatment was carried out with various chemical
or biological compounds and in what quantities
The key that describes the presence of genetic modifications other than the
normal (“wild type”) genotype
This key describes the biological sex of the object of research from which the
sample was taken.</p>
          <p>The key describes the age at which the sample from object of research was taken
Developmental stage</p>
          <p>The key that describes the stage of the life cycle of an object of research at the
time of taking a sample from it
Strain
Source</p>
          <p>Key describing the strain to which the sample belongs.</p>
          <p>A key that describes various characteristics of the sample, such as from what
area the sample was taken from, the sample freshly isolated or frozen, e.t.c.
3</p>
        </sec>
      </sec>
    </sec>
    <sec id="sec-3">
      <title>Results</title>
      <p>The constructed dictionary of cell types and tissues of GTRD currently contains 3954 entries. All cell types and
tissues in the GTRD dictionary were divided into 90 clusters (Figure 2).
Allocation to clusters make it possible to systematize cell types and tissues in the GTRD database according to
anatomical, morphological, and other characteristics. The presence of large clusters, shown in Figure 1, can significantly
simplify the verification of cell types and tissues, speeds up the work with them, and further allows us to analyze
experimental data for experiments from anatomically close areas. For a small number of cell types, there was not enough
information to determine their belonging to any cluster (Other category, Fig. 2).</p>
      <p>For 3225 entries, correspondence was established with the main databases of cell types and tissues presented in Table
1 and this represents more than 80% of all entries in the dictionary. This correspondence was found for most cell types
and tissues (Table 3).
Drosophila melanogaster</p>
      <p>Homo sapiens</p>
      <p>Mus musculus</p>
      <p>Rattus norvegicus</p>
      <p>Saccharomyces cerevisiae
Schizosaccharomyces pombe</p>
      <p>
        Total
described in the GTRD.
No matches were found for 729 records, i.e. these cell types or tissues are found only in the experiments
As result of the comparison of GTRD cell types and tissues with specialized transcription regulation databases
we can show number of matches between GTRD and transcription regulation databases, which presented in Table 4.
comparison made it easy to integrate data for various analyzes, which was demonstrated by us on the data from
FANTOM 5 in the work presented at the MCCMB-2019 conference [
        <xref ref-type="bibr" rid="ref12">12</xref>
        ].
      </p>
      <p>The next step, after compiling the dictionary and comparing thanks to it the cellular types and tissues, was the
development of a system for describing experiments. The introduced new keys, as well as the reworked old ones, allow
to analyze experiments on various grounds, such as sex, age, and others, which opens up new possibilities for data
analysis.
3</p>
    </sec>
    <sec id="sec-4">
      <title>Conclusion</title>
      <p>The dictionary of cell types and tissues that we have developed currently has 82% of the matched cell types
and tissues of all records presented in the GTR, which sets us the task of minimizing the number of unmatched cell
types and tissues.</p>
      <p>1_______________________________________________
for ChIP-seq and DNase-seq experiments
2_______________________________________________
excluding time course experiments
Also an important step will be to introduce for cell types and tissues, a hierarchical system in the future, which will
increase accuracy when comparing experiments from various databases. In addition, the number of experiments in
GTRD increases every year, and them will allow to match more cell types and tissues and as a consequence to
integrate more experiments from transcriptional regulation databases.</p>
      <p>Acknowledgements. This work was supported by the Russian Science Foundation (grant No. 19-14-00295)</p>
    </sec>
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