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<dc:title>Next Generation Sequencing nell'analisi del DNA fetale da plasma materno per la diagnosi prenatale non invasiva di malattie genetiche</dc:title>
<dc:creator>PICCIAU, ANDREA</dc:creator>
<dc:subject>Next Generation</dc:subject>
<dc:subject>diagnosi non invasiva</dc:subject>
<dc:subject>maternal plasma</dc:subject>
<dc:subject>non invasive diagnosis</dc:subject>
<dc:subject>Settore BIO/11 - Biologia Molecolare</dc:subject>
<dc:description>Risk for monogenic disease and aneuploidies are the most common reasons that prompt couples to&#xd;
opt for prenatal diagnosis (PD). Unfortunately, current procedures of prenatal diagnosis are&#xd;
invasive and carry a 0.5-1% risk of fetal mortality. The discovery of fetal DNA in maternal plasma&#xd;
had opened new opportunities for non invasive diagnosis and to date, cffDNA( cell-free fetal&#xd;
DNA) is considered the ideal target to conduct a noninvasive diagnosis (NIPD). Simultaneously,&#xd;
the large develop of next generation technologies (NGS) has provided a robust method to detect&#xd;
and analyze cfDNA (cell free DNA) from maternal plasma. Our intent is develop new protocols&#xd;
able to carry forward a noninvasive diagnosis starting from cffDNA. In this work, we propose a&#xd;
protocol that allow fetal genotype detection from ccfDNA through a target amplification of several&#xd;
SNP and mutation sites, through analysis by Ion Torrent PGM platform technology and supported&#xd;
by statistical approaches useful to discriminate fetal DNA contribution into mixture of&#xd;
fetal/maternal DNA (RHDO/SPRT). In order to define haplotypes we propose a long-range PCR&#xd;
method based that can support the detection of the parental haplotypes in association to normal&#xd;
and mutated alleles. Using these approaches, we have analyzed 18 cfDNA samples with these&#xd;
results: 9 samples correctly defined; 7 samples defined at 50%; 1 sample not correctly defined; 1&#xd;
sample not analyzed. To date, obtained data show that this method is effective and reliable,&#xd;
though will required additional data to confirm these results. Data collected suggest that this&#xd;
method could be inserted, in the near future, in clinical diagnostic practices removing risks of fetal&#xd;
loss, facilitating the diagnostic process and providing significant economic advantage in clinical&#xd;
procedures.</dc:description>
<dc:date>2014-05-30</dc:date>
<dc:type>info:eu-repo/semantics/doctoralThesis</dc:type>
<dc:identifier>http://hdl.handle.net/11584/266531</dc:identifier>
<dc:language>ita</dc:language>
<dc:relation>numberofpages:82</dc:relation>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:publisher>Università degli Studi di Cagliari</dc:publisher>
<dc:rights>license:Non specificato</dc:rights>
</oai_dc:dc></metadata></record></GetRecord></OAI-PMH>