Literature DB >> 34529041

NiPTUNE: an automated pipeline for noninvasive prenatal testing in an accurate, integrative and flexible framework.

Véronique Duboc1, David Pratella2, Marco Milanesio2, John Boudjarane3, Stéphane Descombes2, Véronique Paquis-Flucklinger4, Silvia Bottini5.   

Abstract

Noninvasive prenatal testing (NIPT) consists of determining fetal aneuploidies by quantifying copy number alteration from the sequencing of cell-free DNA (cfDNA) from maternal blood. Due to the presence of cfDNA of fetal origin in maternal blood, in silico approaches have been developed to accurately predict fetal aneuploidies. Although NIPT is becoming a new standard in prenatal screening of chromosomal abnormalities, there are no integrated pipelines available to allow rapid, accurate and standardized data analysis in any clinical setting. Several tools have been developed, however often optimized only for research purposes or requiring enormous amount of retrospective data, making hard their implementation in a clinical context. Furthermore, no guidelines have been provided on how to accomplish each step of the data analysis to achieve reliable results. Finally, there is no integrated pipeline to perform all steps of NIPT analysis. To address these needs, we tested several tools for performing NIPT data analysis. We provide extensive benchmark of tools performances but also guidelines for running them. We selected the best performing tools that we benchmarked and gathered them in a computational pipeline. NiPTUNE is an open source python package that includes methods for fetal fraction estimation, a novel method for accurate gender prediction, a principal component analysis based strategy for quality control and fetal aneuploidies prediction. NiPTUNE is constituted by seven modules allowing the user to run the entire pipeline or each module independently. Using two cohorts composed by 1439 samples with 31 confirmed aneuploidies, we demonstrated that NiPTUNE is a valuable resource for NIPT analysis.
© The Author(s) 2021. Published by Oxford University Press.

Entities:  

Keywords:  benchmark; bioinformatic pipeline; fetal aneuploidies prediction; fetal fraction; prenatal testing

Mesh:

Substances:

Year:  2022        PMID: 34529041      PMCID: PMC8769708          DOI: 10.1093/bib/bbab380

Source DB:  PubMed          Journal:  Brief Bioinform        ISSN: 1467-5463            Impact factor:   11.622


  25 in total

1.  The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes.

Authors:  Helen Skaletsky; Tomoko Kuroda-Kawaguchi; Patrick J Minx; Holland S Cordum; LaDeana Hillier; Laura G Brown; Sjoerd Repping; Tatyana Pyntikova; Johar Ali; Tamberlyn Bieri; Asif Chinwalla; Andrew Delehaunty; Kim Delehaunty; Hui Du; Ginger Fewell; Lucinda Fulton; Robert Fulton; Tina Graves; Shun-Fang Hou; Philip Latrielle; Shawn Leonard; Elaine Mardis; Rachel Maupin; John McPherson; Tracie Miner; William Nash; Christine Nguyen; Philip Ozersky; Kymberlie Pepin; Susan Rock; Tracy Rohlfing; Kelsi Scott; Brian Schultz; Cindy Strong; Aye Tin-Wollam; Shiaw-Pyng Yang; Robert H Waterston; Richard K Wilson; Steve Rozen; David C Page
Journal:  Nature       Date:  2003-06-19       Impact factor: 49.962

2.  WisecondorX: improved copy number detection for routine shallow whole-genome sequencing.

Authors:  Lennart Raman; Annelies Dheedene; Matthias De Smet; Jo Van Dorpe; Björn Menten
Journal:  Nucleic Acids Res       Date:  2019-02-28       Impact factor: 16.971

3.  Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management.

Authors:  Baran Bayindir; Luc Dehaspe; Nathalie Brison; Paul Brady; Simon Ardui; Molka Kammoun; Lars Van der Veken; Klaske Lichtenbelt; Kris Van den Bogaert; Jeroen Van Houdt; Hilde Peeters; Hilde Van Esch; Thomy de Ravel; Eric Legius; Koen Devriendt; Joris R Vermeesch
Journal:  Eur J Hum Genet       Date:  2015-01-14       Impact factor: 4.246

4.  Performance of semiconductor sequencing platform for non-invasive prenatal genetic screening for fetal aneuploidy: results from a multicenter prospective cohort study in a clinical setting.

Authors:  L Allach El Khattabi; S Brun; P Gueguen; N Chatron; E Guichoux; S Schutz; J Nectoux; A Sorlin; M Quere; J Boudjarane; V Tsatsaris; L Mandelbrot; C Schluth-Bolard; J M Dupont; C Rooryck
Journal:  Ultrasound Obstet Gynecol       Date:  2019-08       Impact factor: 7.299

Review 5.  Fetal fraction and noninvasive prenatal testing: What clinicians need to know.

Authors:  Lisa Hui; Diana W Bianchi
Journal:  Prenat Diagn       Date:  2019-12-10       Impact factor: 3.050

6.  Plasma DNA aberrations in systemic lupus erythematosus revealed by genomic and methylomic sequencing.

Authors:  Rebecca W Y Chan; Peiyong Jiang; Xianlu Peng; Lai-Shan Tam; Gary J W Liao; Edmund K M Li; Priscilla C H Wong; Hao Sun; K C Allen Chan; Rossa W K Chiu; Y M Dennis Lo
Journal:  Proc Natl Acad Sci U S A       Date:  2014-11-26       Impact factor: 11.205

7.  Fetal fraction in maternal plasma cell-free DNA at 11-13 weeks' gestation: relation to maternal and fetal characteristics.

Authors:  G Ashoor; A Syngelaki; L C Y Poon; J C Rezende; K H Nicolaides
Journal:  Ultrasound Obstet Gynecol       Date:  2012-12-04       Impact factor: 7.299

8.  Copy number analysis of whole-genome data using BIC-seq2 and its application to detection of cancer susceptibility variants.

Authors:  Ruibin Xi; Semin Lee; Yuchao Xia; Tae-Min Kim; Peter J Park
Journal:  Nucleic Acids Res       Date:  2016-06-03       Impact factor: 16.971

9.  Control-free calling of copy number alterations in deep-sequencing data using GC-content normalization.

Authors:  Valentina Boeva; Andrei Zinovyev; Kevin Bleakley; Jean-Philippe Vert; Isabelle Janoueix-Lerosey; Olivier Delattre; Emmanuel Barillot
Journal:  Bioinformatics       Date:  2010-11-15       Impact factor: 6.937

10.  Calculating the fetal fraction for noninvasive prenatal testing based on genome-wide nucleosome profiles.

Authors:  Roy Straver; Cees B M Oudejans; Erik A Sistermans; Marcel J T Reinders
Journal:  Prenat Diagn       Date:  2016-05-20       Impact factor: 3.050

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  1 in total

1.  GenomeMixer and TRUST: Novel bioinformatics tools to improve reliability of Non-Invasive Prenatal Testing (NIPT) for fetal aneuploidies.

Authors:  David Pratella; Véronique Duboc; Marco Milanesio; John Boudjarane; Stéphane Descombes; Véronique Paquis-Flucklinger; Silvia Bottini
Journal:  Comput Struct Biotechnol J       Date:  2022-02-21       Impact factor: 7.271

  1 in total

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