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Noninvasive prenatal paternity testing by means of SNP‐based targeted sequencing

https://doi.org/10.1002/pd.5595
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/pd.1422openalex-snapshot
Noninvasive genotyping of 9 Y‐chromosome specific STR loci using circulatory fetal DNA in maternal plasma by multiplex PCR
inferredcites →https://doi.org/10.1002/pd.1970121004openalex-snapshot
Genetic diagnosis by chorionic villus sampling before 8 gestational weeks: Efficiency, reliability, and risks on 317 completed pregnancies
inferredcites →https://doi.org/10.1002/pd.3993openalex-snapshot
Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci
inferredcites →https://doi.org/10.1002/pd.5036openalex-snapshot
Noninvasive prenatal screening at low fetal fraction: comparing whole-genome sequencing and single-nucleotide polymorphism methods
inferredcites →https://doi.org/10.1002/pd.5207openalex-snapshot
cfDNA screening and diagnosis of monogenic disorders – where are we heading?
inferredcites →https://doi.org/10.1002/uog.12331openalex-snapshot
Fetal fraction in maternal plasma cell‐free DNA at 11–13 weeks' gestation: relation to maternal and fetal characteristics
inferredcites →https://doi.org/10.1007/s00414-008-0292-9openalex-snapshot
Non-invasive prenatal paternity testing from maternal blood
inferredcites →https://doi.org/10.1007/s004149900117openalex-snapshot
An assessment of the utility of single nucleotide polymorphisms (SNPs) for forensic purposes
inferredcites →https://doi.org/10.1007/s00439-017-1776-9openalex-snapshot
Forensic use of Y-chromosome DNA: a general overview
inferredcites →https://doi.org/10.1016/0168-9525(94)90257-7openalex-snapshot
Paternity testing in the DNA era
inferredcites →https://doi.org/10.1016/j.ajog.2004.05.078openalex-snapshot
Diagnostic mid trimester amniocentesis: How safe?
inferredcites →https://doi.org/10.1016/j.fsigen.2010.02.007openalex-snapshot
Mutations and/or close relatives? Six case work examples where 49 autosomal SNPs were used as supplementary markers
inferredcites →https://doi.org/10.1016/j.fsigen.2014.11.006openalex-snapshot
Fetal male lineage determination by analysis of Y-chromosome STR haplotype in maternal plasma
inferredcites →https://doi.org/10.1016/j.legalmed.2018.03.009openalex-snapshot
Non-invasive prenatal paternity testing using cell-free fetal DNA from maternal plasma: DNA isolation and genetic marker studies
inferredcites →https://doi.org/10.1016/s0140-6736(97)02174-0openalex-snapshot
Presence of fetal DNA in maternal plasma and serum
inferredcites →https://doi.org/10.1038/gim.2012.155openalex-snapshot
Informatics-based, highly accurate, noninvasive prenatal paternity testing
inferredcites →https://doi.org/10.1038/gim.2017.186openalex-snapshot
Informative priors on fetal fraction increase power of the noninvasive prenatal screen
inferredcites →https://doi.org/10.1093/bioinformatics/btq040openalex-snapshot
SNVMix: predicting single nucleotide variants from next-generation sequencing of tumors
inferredcites →https://doi.org/10.1093/bioinformatics/bts549openalex-snapshot
FetalQuant: deducing fractional fetal DNA concentration from massively parallel sequencing of DNA in maternal plasma
inferredcites →https://doi.org/10.1093/bioinformatics/bty790openalex-snapshot
smCounter2: an accurate low-frequency variant caller for targeted sequencing data with unique molecular identifiers
inferredcites →https://doi.org/10.1097/01.aog.0000291570.63450.44openalex-snapshot
ACOG Practice Bulletin No. 88: Invasive Prenatal Testing for Aneuploidy
inferredcites →https://doi.org/10.1111/j.1399-0004.2010.01533.xopenalex-snapshot
Non-invasive prenatal determination of fetal sex: translating research into clinical practice
inferredcites →https://doi.org/10.1111/j.1537-2995.2005.00559.xopenalex-snapshot
Noninvasive determination of fetalRHDstatus by examination of cell‐free DNA in maternal plasma
inferredcites →https://doi.org/10.1111/trf.14077openalex-snapshot
Noninvasive fetal genotyping of paternally inherited alleles using targeted massively parallel sequencing in parentage testing cases
inferredcites →https://doi.org/10.1111/trf.14577openalex-snapshot
Noninvasive prenatal paternity testing using targeted massively parallel sequencing
inferredcites →https://doi.org/10.1136/bmj.c7401openalex-snapshot
Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study
inferredcites →https://doi.org/10.1159/000075150openalex-snapshot
Maternal Mortality following Diagnostic 2nd-Trimester Amniocentesis
inferredcites →https://doi.org/10.1166/jbn.2013.1568openalex-snapshot
An Automatic High-Throughput Single Nucleotide Polymorphism Genotyping Approach Based on Universal Tagged Arrays and Magnetic Nanoparticles
inferredcites →https://doi.org/10.1201/9781420037920openalex-snapshot
Forensic DNA Evidence Interpretation
inferredcites →https://doi.org/10.1371/journal.pone.0146638openalex-snapshot
Benefits and Challenges with Applying Unique Molecular Identifiers in Next Generation Sequencing to Detect Low Frequency Mutations
inferredcites →https://doi.org/10.1371/journal.pone.0159385openalex-snapshot
Noninvasive Prenatal Paternity Testing (NIPAT) through Maternal Plasma DNA Sequencing: A Pilot Study
inferredcites →https://doi.org/10.3390/ijms13055972openalex-snapshot
Multiplex PCR for 17 Y-Chromosome Specific Short Tandem Repeats (STR) to Enhance the Reliability of Fetal Sex Determination in Maternal Plasma
inferredcites →https://doi.org/10.7150/thno.5032openalex-snapshot
A Novel SNPs Detection Method Based on Gold Magnetic Nanoparticles Array and Single Base Extension

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4758749openalex-extracted
Pedigree Reconstruction Based on Target Sequencing in Pacific White Shrimp Litopeneaus Vannamei
inferred← citeshttps://doi.org/10.1002/elps.202400119openalex-snapshot
Developmental Validation of a DIP‐InDel/DIP‐STR System for the Detection of Unbalanced DNA Mixtures
inferred← citeshttps://doi.org/10.1002/elps.70021openalex-snapshot
Evaluation of an MPS‐Based Microhaplotype Assay for Non‐Invasive Prenatal Paternity Testing
inferred← citeshttps://doi.org/10.1016/b978-0-323-99144-5.00008-1openalex-snapshot
Application of NGS technology for parentage testing and relatedness analysis
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2023.739728openalex-snapshot
Development of an informative SNP panel for molecular parentage analysis in large yellow croaker (Larimichthys crocea)
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2024.741375openalex-snapshot
Pedigree reconstruction based on target sequencing in Pacific white shrimp Litopenaeus vannamei
inferred← citeshttps://doi.org/10.1016/j.forsciint.2023.111649openalex-snapshot
A theoretical base for non-invasive prenatal paternity testing
inferred← citeshttps://doi.org/10.1016/j.forsciint.2023.111848openalex-snapshot
Construction and evaluation of a novel set of 90 microhaplotypes for forensic applications using NGS technology
inferred← citeshttps://doi.org/10.1016/j.forsciint.2025.112594openalex-snapshot
Evaluation of a hybridization capture-based hereditary panel for forensic DNA analysis using next-generation sequencing
inferred← citeshttps://doi.org/10.1016/j.fsigen.2020.102338openalex-snapshot
Noninvasive prenatal paternity testing by target sequencing microhaps
inferred← citeshttps://doi.org/10.1016/j.mam.2024.101253openalex-snapshot
Principles of digital sequencing using unique molecular identifiers
inferred← citeshttps://doi.org/10.1038/s41598-023-39367-0openalex-snapshot
Early noninvasive prenatal paternity testing by targeted fetal DNA analysis
inferred← citeshttps://doi.org/10.1093/bfgp/elac024openalex-snapshot
Digital PCR and its applications in noninvasive prenatal testing
inferred← citeshttps://doi.org/10.1111/bjh.19197openalex-snapshot
Feasibility for non‐invasive prenatal fetal blood group and platelet genotyping by massively parallel sequencing: A single test system for multiple atypical red cell, platelet and quality control markers
inferred← citeshttps://doi.org/10.1111/trf.14577openalex-snapshot
Noninvasive prenatal paternity testing using targeted massively parallel sequencing
inferred← citeshttps://doi.org/10.1186/s12920-020-00806-wopenalex-snapshot
Noninvasive prenatal paternity determination using microhaplotypes: a pilot study
inferred← citeshttps://doi.org/10.1186/s13104-021-05793-4openalex-snapshot
Improved library preparation protocols for amplicon sequencing-based noninvasive fetal genotyping for RHD-positive D antigen-negative alleles
inferred← citeshttps://doi.org/10.1371/journal.pone.0266332openalex-snapshot
Non-invasive prenatal paternity testing by analysis of Y-chromosome mini-STR haplotype using next-generation sequencing
inferred← citeshttps://doi.org/10.1515/labmed-2021-0191openalex-snapshot
Non-invasive prenatal paternity testing using mini-STR-based next-generation sequencing: a pilot study
inferred← citeshttps://doi.org/10.20517/jtgg.2024.46openalex-snapshot
A novel SNP-based approach for non-invasive prenatal paternity testing using multiplex PCR targeted capture sequencing
inferred← citeshttps://doi.org/10.2147/ijn.s479297openalex-snapshot
Non-Invasive Prenatal Diagnosis of Chromosomal and Monogenic Disease by a Novel Bioinspired Micro–Nanochip for Isolating Fetal Nucleated Red Blood Cells
inferred← citeshttps://doi.org/10.22541/au.164864542.28963224/v1openalex-snapshot
Non-invasive prenatal paternity testing using mini-STR-based next-generation sequencing: a methodological study
inferred← citeshttps://doi.org/10.3389/fgene.2021.800598openalex-snapshot
Set of 15 SNP-SNP Markers for Detection of Unbalanced Degraded DNA Mixtures and Noninvasive Prenatal Paternity Testing
inferred← citeshttps://doi.org/10.3389/fgene.2024.1401898openalex-snapshot
Bibliometric analysis of kinship analysis from 1960 to 2023: global trends and development
inferred← citeshttps://doi.org/10.3390/biotech10030017openalex-snapshot
Calculation of Fetal Fraction for Non-Invasive Prenatal Testing
inferred← citeshttps://doi.org/10.3390/genes12010026openalex-snapshot
Evaluation of a Microhaplotype-Based Noninvasive Prenatal Test in Twin Gestations: Determination of Paternity, Zygosity, and Fetal Fraction
inferred← citeshttps://doi.org/10.3390/genes14040818openalex-snapshot
Applying Unique Molecular Indices with an Extensive All-in-One Forensic SNP Panel for Improved Genotype Accuracy and Sensitivity
inferred← citeshttps://doi.org/10.3390/genes14071357openalex-snapshot
Low-Pass Genome Sequencing-Based Detection of Paternity: Validation in Clinical Cytogenetics
inferred← citeshttps://doi.org/10.3390/genes16030311openalex-snapshot
Identification of a Homozygous Variant in the CYP21A2 Gene by Next-Generation Sequencing Analysis of Circulating Cell-Free Fetal DNA
inferred← citeshttps://doi.org/10.3390/ijms26104518openalex-snapshot
Noninvasive Prenatal Paternity Testing: A Review on Genetic Markers
inferred← citeshttps://doi.org/10.5772/intechopen.97670openalex-snapshot
Obstetric Markers as a Diagnostic Forensic Tool
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