MaterniCode: New Bioinformatic Pipeline to Detect Fetal Aneuploidies and Rearrangements Using Next-Generation Sequencing

Conclusion: MaterniCode has proven to be an innovative and highly efficient tool in the domain of NIPT, demonstrating excellent sensitivity and specificity. Its robust capability to effectively detect a wide range of complex chromosomal aberrations, including rare and subtle variations, positions it...

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Main Authors: Federico Gabrielli, Filomena Tiziana Papa, Fabio Di Pietro, Andreu Paytuví-Gallart, Daniel Julian, Walter Sanseverino, Cinzia Alfonsi
Format: Article
Language:English
Published: Wiley 2024-01-01
Series:International Journal of Genomics
Online Access:http://dx.doi.org/10.1155/2024/8859058
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author Federico Gabrielli
Filomena Tiziana Papa
Fabio Di Pietro
Andreu Paytuví-Gallart
Daniel Julian
Walter Sanseverino
Cinzia Alfonsi
author_facet Federico Gabrielli
Filomena Tiziana Papa
Fabio Di Pietro
Andreu Paytuví-Gallart
Daniel Julian
Walter Sanseverino
Cinzia Alfonsi
author_sort Federico Gabrielli
collection DOAJ
description Conclusion: MaterniCode has proven to be an innovative and highly efficient tool in the domain of NIPT, demonstrating excellent sensitivity and specificity. Its robust capability to effectively detect a wide range of complex chromosomal aberrations, including rare and subtle variations, positions it as a promising and valuable addition to prenatal diagnostic technologies. This enhancement to diagnostic precision significantly aids clinicians in making informed decisions during pregnancy management.
format Article
id doaj-art-bcc8d43d62f84f60a2097bf4b99491a3
institution Kabale University
issn 2314-4378
language English
publishDate 2024-01-01
publisher Wiley
record_format Article
series International Journal of Genomics
spelling doaj-art-bcc8d43d62f84f60a2097bf4b99491a32025-02-03T07:23:38ZengWileyInternational Journal of Genomics2314-43782024-01-01202410.1155/2024/8859058MaterniCode: New Bioinformatic Pipeline to Detect Fetal Aneuploidies and Rearrangements Using Next-Generation SequencingFederico Gabrielli0Filomena Tiziana Papa1Fabio Di Pietro2Andreu Paytuví-Gallart3Daniel Julian4Walter Sanseverino5Cinzia Alfonsi6Biolab srl, Laboratorio di Genetica molecolare e GenomicaBiolab srl, Laboratorio di Genetica molecolare e GenomicaBiolab srl, Laboratorio di Genetica molecolare e GenomicaSequentia Biotech SLSequentia Biotech SLSequentia Biotech SLBiolab srl, Laboratorio di Genetica molecolare e GenomicaConclusion: MaterniCode has proven to be an innovative and highly efficient tool in the domain of NIPT, demonstrating excellent sensitivity and specificity. Its robust capability to effectively detect a wide range of complex chromosomal aberrations, including rare and subtle variations, positions it as a promising and valuable addition to prenatal diagnostic technologies. This enhancement to diagnostic precision significantly aids clinicians in making informed decisions during pregnancy management.http://dx.doi.org/10.1155/2024/8859058
spellingShingle Federico Gabrielli
Filomena Tiziana Papa
Fabio Di Pietro
Andreu Paytuví-Gallart
Daniel Julian
Walter Sanseverino
Cinzia Alfonsi
MaterniCode: New Bioinformatic Pipeline to Detect Fetal Aneuploidies and Rearrangements Using Next-Generation Sequencing
International Journal of Genomics
title MaterniCode: New Bioinformatic Pipeline to Detect Fetal Aneuploidies and Rearrangements Using Next-Generation Sequencing
title_full MaterniCode: New Bioinformatic Pipeline to Detect Fetal Aneuploidies and Rearrangements Using Next-Generation Sequencing
title_fullStr MaterniCode: New Bioinformatic Pipeline to Detect Fetal Aneuploidies and Rearrangements Using Next-Generation Sequencing
title_full_unstemmed MaterniCode: New Bioinformatic Pipeline to Detect Fetal Aneuploidies and Rearrangements Using Next-Generation Sequencing
title_short MaterniCode: New Bioinformatic Pipeline to Detect Fetal Aneuploidies and Rearrangements Using Next-Generation Sequencing
title_sort maternicode new bioinformatic pipeline to detect fetal aneuploidies and rearrangements using next generation sequencing
url http://dx.doi.org/10.1155/2024/8859058
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