Synthesis of positive plasmas with known chromosomal abnormalities for validation of non-invasive prenatal screening

Non-invasive prenatal screening (NIPS) is a DNA sequencing-based screening test for fetal aneuploidies and possibly other pathogenic genomic abnormalities, such as large deletions and duplications. Validation and quality assurance (QA) of this clinical test using plasmas with and without targeted ch...

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Main Authors: Zhongxia Qi, Jingwei Yu
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-01-01
Series:Frontiers in Genetics
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2023.971087/full
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author Zhongxia Qi
Jingwei Yu
author_facet Zhongxia Qi
Jingwei Yu
author_sort Zhongxia Qi
collection DOAJ
description Non-invasive prenatal screening (NIPS) is a DNA sequencing-based screening test for fetal aneuploidies and possibly other pathogenic genomic abnormalities, such as large deletions and duplications. Validation and quality assurance (QA) of this clinical test using plasmas with and without targeted chromosomal abnormalities from pregnant women as negative and positive controls are required. However, the positive plasma controls may not be available for many laboratories that are planning to establish NIPS. Limited synthetic positive plasmas are commercially available, but the types of abnormalities and the number/quantity of synthetic plasmas for each abnormality are insufficient to meet the minimal requirements for the initial validation. We report here a method of making synthetic positive plasmas by adding cell-free DNA (cfDNA) isolated from culture media of prenatal cells with chromosomal abnormalities to the plasmas from non-pregnant women. Thirty-eight positive plasmas with various chromosomal abnormalities, including autosomal and sex chromosomal aneuploidies, large deletions and duplications, were synthesized. The synthetic plasmas were characterized side-by-side with real positive plasmas from pregnant women and commercially available synthetic positive plasmas using the Illumina VeriSeq NIPT v2 system. All chromosomal abnormalities in the synthetic plasmas were correctly identified with the same testing sensitivity and specificity as in the real and commercial synthetic plasmas. The findings demonstrate that the synthetic positive plasmas are excellent alternatives of real positive plasmas for validation and QA of NIPS. The method described here is simple and straightforward, and can be readily used in clinical genetics laboratories with accessibility to prenatal cultures.
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spelling doaj.art-36ac3fe33e9c4ac0aef36cb9c42056e22023-01-16T05:27:04ZengFrontiers Media S.A.Frontiers in Genetics1664-80212023-01-011410.3389/fgene.2023.971087971087Synthesis of positive plasmas with known chromosomal abnormalities for validation of non-invasive prenatal screeningZhongxia QiJingwei YuNon-invasive prenatal screening (NIPS) is a DNA sequencing-based screening test for fetal aneuploidies and possibly other pathogenic genomic abnormalities, such as large deletions and duplications. Validation and quality assurance (QA) of this clinical test using plasmas with and without targeted chromosomal abnormalities from pregnant women as negative and positive controls are required. However, the positive plasma controls may not be available for many laboratories that are planning to establish NIPS. Limited synthetic positive plasmas are commercially available, but the types of abnormalities and the number/quantity of synthetic plasmas for each abnormality are insufficient to meet the minimal requirements for the initial validation. We report here a method of making synthetic positive plasmas by adding cell-free DNA (cfDNA) isolated from culture media of prenatal cells with chromosomal abnormalities to the plasmas from non-pregnant women. Thirty-eight positive plasmas with various chromosomal abnormalities, including autosomal and sex chromosomal aneuploidies, large deletions and duplications, were synthesized. The synthetic plasmas were characterized side-by-side with real positive plasmas from pregnant women and commercially available synthetic positive plasmas using the Illumina VeriSeq NIPT v2 system. All chromosomal abnormalities in the synthetic plasmas were correctly identified with the same testing sensitivity and specificity as in the real and commercial synthetic plasmas. The findings demonstrate that the synthetic positive plasmas are excellent alternatives of real positive plasmas for validation and QA of NIPS. The method described here is simple and straightforward, and can be readily used in clinical genetics laboratories with accessibility to prenatal cultures.https://www.frontiersin.org/articles/10.3389/fgene.2023.971087/fullnon-invasive prenatal screening (NIPS)synthetic plasmaNIPS validationcell free DNAfetal fraction
spellingShingle Zhongxia Qi
Jingwei Yu
Synthesis of positive plasmas with known chromosomal abnormalities for validation of non-invasive prenatal screening
Frontiers in Genetics
non-invasive prenatal screening (NIPS)
synthetic plasma
NIPS validation
cell free DNA
fetal fraction
title Synthesis of positive plasmas with known chromosomal abnormalities for validation of non-invasive prenatal screening
title_full Synthesis of positive plasmas with known chromosomal abnormalities for validation of non-invasive prenatal screening
title_fullStr Synthesis of positive plasmas with known chromosomal abnormalities for validation of non-invasive prenatal screening
title_full_unstemmed Synthesis of positive plasmas with known chromosomal abnormalities for validation of non-invasive prenatal screening
title_short Synthesis of positive plasmas with known chromosomal abnormalities for validation of non-invasive prenatal screening
title_sort synthesis of positive plasmas with known chromosomal abnormalities for validation of non invasive prenatal screening
topic non-invasive prenatal screening (NIPS)
synthetic plasma
NIPS validation
cell free DNA
fetal fraction
url https://www.frontiersin.org/articles/10.3389/fgene.2023.971087/full
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