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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">medgen</journal-id><journal-title-group><journal-title xml:lang="ru">Медицинская генетика</journal-title><trans-title-group xml:lang="en"><trans-title>Medical Genetics</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2073-7998</issn><publisher><publisher-name>Publishing House «Genius Media» LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.25557/2073-7998.2020.03.69-70</article-id><article-id custom-type="elpub" pub-id-type="custom">medgen-837</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>КРАТКИЕ СООБЩЕНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>BRIEF REPORT</subject></subj-group></article-categories><title-group><article-title>Неинвазивный пренатальный ДНК-скрининг - возможности и перспективы полногеномного подхода</article-title><trans-title-group xml:lang="en"><trans-title>Nonivasive prenatal DNA-screening the scope and the prospects of whole-genome sequencing</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Шубина</surname><given-names>Е. .</given-names></name><name name-style="western" xml:lang="en"><surname>Shubina</surname><given-names>J. .</given-names></name></name-alternatives><email xlink:type="simple">jekaterina.shubina@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Барков</surname><given-names>И. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Barkov</surname><given-names>I. Yu.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Гольцов</surname><given-names>А. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Goltsov</surname><given-names>A. Yu.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Мукосей</surname><given-names>И. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Mukosey</surname><given-names>I. S.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кочеткова</surname><given-names>Т. О.</given-names></name><name name-style="western" xml:lang="en"><surname>Kochetkova</surname><given-names>T. O.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ступко</surname><given-names>О. К.</given-names></name><name name-style="western" xml:lang="en"><surname>Stupko</surname><given-names>O. K.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Трофимов</surname><given-names>Д. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Trofimov</surname><given-names>D. Yu.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБУ «Научный медицинский исследовательский центр акушерства, гинекологии и перинатологии им. В.И.Кулакова»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>FBSI «National medical research center for obstetrics, gynecology and perinatology named after academician V.I. Kulakov»</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2020</year></pub-date><pub-date pub-type="epub"><day>01</day><month>09</month><year>2020</year></pub-date><volume>19</volume><issue>3</issue><fpage>69</fpage><lpage>70</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Шубина Е..., Барков И.Ю., Гольцов А.Ю., Мукосей И.С., Кочеткова Т.О., Ступко О.К., Трофимов Д.Ю., 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">Шубина Е..., Барков И.Ю., Гольцов А.Ю., Мукосей И.С., Кочеткова Т.О., Ступко О.К., Трофимов Д.Ю.</copyright-holder><copyright-holder xml:lang="en">Shubina J..., Barkov I.Y., Goltsov A.Y., Mukosey I.S., Kochetkova T.O., Stupko O.K., Trofimov D.Y.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.medgen-journal.ru/jour/article/view/837">https://www.medgen-journal.ru/jour/article/view/837</self-uri><abstract><p>Неинвазивный пренатальный ДНК-скрининг (НИПС) начал использоваться в клинической практике в 2011г. и в настоящее время широко применяется, как и в мире, так и в России. Проанализирована встречаемость «редких» анеуплоидий при проведении полногеномного НИПС у 2061 пациенток и исходы беременностей при наличии таких результатов. Показано, что при анализе всего генома для полногеномного варианта НИПС можно получить дополнительную информацию, важную как для прогноза течения беременности, так и для прогноза плода. Это позволяет выделить дополнительную небольшую группу беременных, которым может быть рекомендовано более пристальное наблюдение в течение беременности или проведение дополнительных диагностических процедур. Однако для определения чувствительности и специфичности определения «редких» анеуплодий и CNV в настоящий момент недостаточно данных.</p></abstract><trans-abstract xml:lang="en"><p>Noninvasive prenatal DNA screening (NIPS) is getting more widespread in clinical practice in Russia and all around the world. The use of shallow whole-genome sequencing for NIPS allows analysis of all chromosome aneuploidies; hence there are large-scale studies only on test performance on common trisomies. This study aimed to analyze the prevalence of «rare» aneuploidies using whole-genome NIPS and pregnancy outcomes in case of a high risk of «rare» aneuploidy. Noninvasive prenatal DNA screening was performed using in house developed protocol. We have analyzed 2061 samples. In 8 cases (0.4%) high-risk of rare trisomy was detected (3 - trisomy 7, 2 - trisomy 8, 1 - trisomy 10, 2 - trisomy 15). We have identified two cases of a high risk of large copy number variations (CNV). For all of the high-risk cases, we have information about pregnancy outcomes. Thereby whole-genome analysis will enable us to get the additional information and reveal pregnancies in need of further observation or testing. Hence there is not enough data for the estimation of sensitivity and specificity of detection of «rare» aneuploidies.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>НИПС</kwd><kwd>НИПТ</kwd><kwd>редкие анеуплоидии</kwd><kwd>синдром Прадера-Вилли</kwd><kwd>NIPS</kwd><kwd>NIPT</kwd><kwd>rare aneuploidy</kwd><kwd>Prader Willi syndrome</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
