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<article article-type="research-article" dtd-version="1.2" xml:lang="ru" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"><front><journal-meta><journal-id journal-id-type="issn">2658-6533</journal-id><journal-title-group><journal-title>Research Results in Biomedicine</journal-title></journal-title-group><issn pub-type="epub">2658-6533</issn></journal-meta><article-meta><article-id pub-id-type="doi">10.18413/2658-6533-2020-6-1-0-1</article-id><article-id pub-id-type="publisher-id">1957</article-id><article-categories><subj-group subj-group-type="heading"><subject>Genetics</subject></subj-group></article-categories><title-group><article-title>&lt;strong&gt;New data collection priority: focusing on genome-based bioinformation&lt;/strong&gt;</article-title><trans-title-group xml:lang="en"><trans-title>&lt;strong&gt;New data collection priority: focusing on genome-based bioinformation&lt;/strong&gt;</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Heng</surname><given-names>Henry H.</given-names></name><name xml:lang="en"><surname>Heng</surname><given-names>Henry H.</given-names></name></name-alternatives><email>hheng@med.wayne.edu</email></contrib></contrib-group><pub-date pub-type="epub"><year>2020</year></pub-date><volume>6</volume><issue>1</issue><fpage>0</fpage><lpage>0</lpage><self-uri content-type="pdf" xlink:href="/media/medicine/2020/1/document_март_2020-6-9.pdf" /><abstract xml:lang="ru"><p>Genetic research used to be data-driven under the framework of well-established gene theory. With the advance of various-omics technologies, large-scale data generation has become routine. However, data analyses have unexpectedly become extremely challenging due to the highly heterogeneous nature of bio-data. Furthermore, these diverse data sets seem to be inconsistent with some key predictions of gene theory. To briefly address this new reality, this editorial suggests a new genome theory to explain the new facts. By briefly comparing cytogenetics and gene sequencing research, the importance and key principles of chromosomal coded bioinformation is highlighted in the context of evolutionary studies and disease research. </p></abstract><trans-abstract xml:lang="en"><p>Genetic research used to be data-driven under the framework of well-established gene theory. With the advance of various-omics technologies, large-scale data generation has become routine. However, data analyses have unexpectedly become extremely challenging due to the highly heterogeneous nature of bio-data. Furthermore, these diverse data sets seem to be inconsistent with some key predictions of gene theory. To briefly address this new reality, this editorial suggests a new genome theory to explain the new facts. By briefly comparing cytogenetics and gene sequencing research, the importance and key principles of chromosomal coded bioinformation is highlighted in the context of evolutionary studies and disease research. </p></trans-abstract><kwd-group xml:lang="ru"><kwd>genome chaos</kwd><kwd>genome theory</kwd><kwd>karyotype coding</kwd><kwd>missing heritability</kwd><kwd>non clonal chromosome aberrations</kwd><kwd>system inheritance</kwd><kwd>two-phases of cancer evolution</kwd></kwd-group><kwd-group xml:lang="en"><kwd>genome chaos</kwd><kwd>genome theory</kwd><kwd>karyotype coding</kwd><kwd>missing heritability</kwd><kwd>non clonal chromosome aberrations</kwd><kwd>system inheritance</kwd><kwd>two-phases of cancer evolution</kwd></kwd-group></article-meta></front><back><ref-list><title>Список литературы</title><ref id="B1"><mixed-citation>Heng HH. Genome Chaos: Rethinking Genetics, Evolution, and Molecular Medicine. 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