NIPT FOR TRACKING AND COMPUTERISED SYSTEMS IN FRIULI VENEZIA GIULIA (BORN IN FVG) (Q2031395)
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Project Q2031395 in Italy
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | NIPT FOR TRACKING AND COMPUTERISED SYSTEMS IN FRIULI VENEZIA GIULIA (BORN IN FVG) |
Project Q2031395 in Italy |
Statements
62,832.12 Euro
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125,664.24 Euro
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50.0 percent
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22 July 2016
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1 August 2019
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DIPARTIMENTO SCIENZE DELLA VITA
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45°40'37.52"N, 13°45'12.31"E
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A PARTIRE DAL PRIMO TRIMESTRE DI GRAVIDANZA Ê PRESENTE NEL CIRCOLO EMATICO MATERNO DNA FETALE CHE PUò ESSERE RECUPERATO IN MANIERA NON-INVASIVA ED ESSERE UTILIZZATO PER LO SCREENING DI ALCUNE PATOLOGIE GENETICHE DOVUTE AD ABERRAZIONI CROMOSOMICHE (NON INVASIVE PRENATAL DIAGNOSIS, NIPT). L¿INTERVENTO SI PONE DUE OBIETTIVI: I) LO SVILUPPO DI METODI CHE CONSENTANO LA STIMA DELLA FRAZIONE FETALE; II) L¿ESTENSIONE DELL¿ANALISI NIPT AD ANEUPLODIE CROMOSOMICHE AGGIUNTIVE RISPETTO AI TEST IN US (Italian)
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FROM THE FIRST TRIMESTER, THIS WAS TAKEN INTO ACCOUNT IN THE MATERNAL DNA RING, WHICH CAN BE RECOVERED AND USED TO SCREEN FOR CERTAIN GENETIC DISEASES DUE TO CHROMOSOMAL ABERRATIONS (NON-INVASIVE PRENATAL DIAGNOSIS, NIPT). THIS INTERVENTION HAS TWO OBJECTIVES: (I) THE DEVELOPMENT OF METHODS ENABLING THE ESTIMATE OF THE FOETAL FRACTION; (II) Â OF THE EXTENSION OF THE NIPT ANALYSIS TO ANEUPLODIE CHROMOSOME TO THE US TEST (English)
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DÈS LE PREMIER TRIMESTRE DE LA GROSSESSE Š PRÉSENTE DANS LE CYCLE DU SANG MATERNEL ADN FOETAL QUI PEUT ÊTRE RÉCUPÉRÉ DE MANIÈRE NON INVASIVE ET UTILISÉ POUR LE DÉPISTAGE DE CERTAINES MALADIES GÉNÉTIQUES DUES À DES ABERRATIONS CHROMOSOMIQUES (DIAGNOSTIC PRÉNATAL NON ENVAHISSANT, NIPT). L’INTERVENTION POURSUIT DEUX OBJECTIFS: L’ÉLABORATION DE MÉTHODES D’ESTIMATION DE LA FRACTION FŒTALE; L’EXTENSION DE L’ANALYSE NIPT À DES ANEUPLODIES CHROMOSOMIQUES SUPPLÉMENTAIRES PAR RAPPORT À NOUS TESTS (French)
15 December 2021
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VANAF HET EERSTE TRIMESTER VAN DE ZWANGERSCHAP Ê AANWEZIG IN DE BLOEDCYCLUS FOETALE DNA VAN DE MOEDER DIE OP EEN NIET-INVASIEVE MANIER KAN WORDEN HERSTELD EN GEBRUIKT VOOR DE SCREENING VAN BEPAALDE GENETISCHE ZIEKTEN ALS GEVOLG VAN CHROMOSOMALE AFWIJKINGEN (NIET-INVASIEVE PRENATALE DIAGNOSE, NIPT). DE INTERVENTIE HEEFT TWEE DOELSTELLINGEN: DE ONTWIKKELING VAN METHODEN VOOR HET SCHATTEN VAN DE FOETALE FRACTIE; DE UITBREIDING VAN NIPT-ANALYSE NAAR EXTRA CHROMOSOMALE ANEUPLODIES IN VERGELIJKING MET ONS TESTEN (Dutch)
23 December 2021
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Identifiers
J96G17000090005
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