Improved noninvasive fetal variant calling using standardized benchmarking approaches

The technology of noninvasive prenatal testing (NIPT) enables risk-free detection of genetic conditions in the fetus, by analysis of cell-free DNA (cfDNA) in maternal blood. For chromosomal abnormalities, NIPT often effectively replaces invasive tests (e.g. amniocentesis), although it is considered...

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Main Authors: Tom Rabinowitz, Shira Deri-Rozov, Noam Shomron
Format: Article
Language:English
Published: Elsevier 2021-01-01
Series:Computational and Structural Biotechnology Journal
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2001037020305572
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spelling doaj-6c7be39824a844cdac28546adf2a008c2021-01-10T04:10:23ZengElsevierComputational and Structural Biotechnology Journal2001-03702021-01-0119509517Improved noninvasive fetal variant calling using standardized benchmarking approachesTom Rabinowitz0Shira Deri-Rozov1Noam Shomron2Faculty of Medicine, Tel Aviv University, Tel Aviv 69978, IsraelFaculty of Medicine, Tel Aviv University, Tel Aviv 69978, IsraelCorresponding author.; Faculty of Medicine, Tel Aviv University, Tel Aviv 69978, IsraelThe technology of noninvasive prenatal testing (NIPT) enables risk-free detection of genetic conditions in the fetus, by analysis of cell-free DNA (cfDNA) in maternal blood. For chromosomal abnormalities, NIPT often effectively replaces invasive tests (e.g. amniocentesis), although it is considered as screening rather than diagnostics. Most recently, the NIPT has been applied to genome-wide, comprehensive genotyping of the fetus using cfDNA, i.e. identifying all its genetic variants and mutations. Previously, we suggested that NIPD should be treated as a special case of variant calling, and presented Hoobari, the first software tool for noninvasive fetal variant calling. Using a unique pipeline, we were able to comprehensively decipher the inheritance of SNPs and indels. A few caveats still exist in this pipeline. Performance was lower for indels and biparental loci (i.e. where both parents carry the same mutation), and performance was not uniform across the genome. Here we utilized standardized methods for benchmarking of variant calling pipelines and applied them to noninvasive fetal variant calling. By using the best performing pipeline and by focusing on coding regions, we showed that noninvasive fetal genotyping greatly improves performance, particularly in indels and biparental loci. These results emphasize the importance of using widely accepted concepts to describe the challenge of genome-wide NIPT of point mutations; and demonstrate a benchmarking process for the first time in this field. This study brings genome-wide and complete NIPD closer to the clinic; while potentially alleviating uncertainty and anxiety during pregnancy, and promoting informed choices among families and physicians.http://www.sciencedirect.com/science/article/pii/S2001037020305572Noninvasive prenatal diagnosisVariant callingNIPTNIPDcell-free DNAcfDNA
collection DOAJ
language English
format Article
sources DOAJ
author Tom Rabinowitz
Shira Deri-Rozov
Noam Shomron
spellingShingle Tom Rabinowitz
Shira Deri-Rozov
Noam Shomron
Improved noninvasive fetal variant calling using standardized benchmarking approaches
Computational and Structural Biotechnology Journal
Noninvasive prenatal diagnosis
Variant calling
NIPT
NIPD
cell-free DNA
cfDNA
author_facet Tom Rabinowitz
Shira Deri-Rozov
Noam Shomron
author_sort Tom Rabinowitz
title Improved noninvasive fetal variant calling using standardized benchmarking approaches
title_short Improved noninvasive fetal variant calling using standardized benchmarking approaches
title_full Improved noninvasive fetal variant calling using standardized benchmarking approaches
title_fullStr Improved noninvasive fetal variant calling using standardized benchmarking approaches
title_full_unstemmed Improved noninvasive fetal variant calling using standardized benchmarking approaches
title_sort improved noninvasive fetal variant calling using standardized benchmarking approaches
publisher Elsevier
series Computational and Structural Biotechnology Journal
issn 2001-0370
publishDate 2021-01-01
description The technology of noninvasive prenatal testing (NIPT) enables risk-free detection of genetic conditions in the fetus, by analysis of cell-free DNA (cfDNA) in maternal blood. For chromosomal abnormalities, NIPT often effectively replaces invasive tests (e.g. amniocentesis), although it is considered as screening rather than diagnostics. Most recently, the NIPT has been applied to genome-wide, comprehensive genotyping of the fetus using cfDNA, i.e. identifying all its genetic variants and mutations. Previously, we suggested that NIPD should be treated as a special case of variant calling, and presented Hoobari, the first software tool for noninvasive fetal variant calling. Using a unique pipeline, we were able to comprehensively decipher the inheritance of SNPs and indels. A few caveats still exist in this pipeline. Performance was lower for indels and biparental loci (i.e. where both parents carry the same mutation), and performance was not uniform across the genome. Here we utilized standardized methods for benchmarking of variant calling pipelines and applied them to noninvasive fetal variant calling. By using the best performing pipeline and by focusing on coding regions, we showed that noninvasive fetal genotyping greatly improves performance, particularly in indels and biparental loci. These results emphasize the importance of using widely accepted concepts to describe the challenge of genome-wide NIPT of point mutations; and demonstrate a benchmarking process for the first time in this field. This study brings genome-wide and complete NIPD closer to the clinic; while potentially alleviating uncertainty and anxiety during pregnancy, and promoting informed choices among families and physicians.
topic Noninvasive prenatal diagnosis
Variant calling
NIPT
NIPD
cell-free DNA
cfDNA
url http://www.sciencedirect.com/science/article/pii/S2001037020305572
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