Cargando…

Set of 15 SNP-SNP Markers for Detection of Unbalanced Degraded DNA Mixtures and Noninvasive Prenatal Paternity Testing

Unbalanced and degraded mixtures (UDM) are very common in forensic DNA analysis. For example, DNA signals from criminal suspects are masked by a large amount of DNA from victims, or cell-free fetal DNA (cffDNA) in maternal plasma is masked by a high background of maternal DNA. Currently, detecting m...

Descripción completa

Detalles Bibliográficos
Autores principales:	Zhang, Rangran, Tan, Yu, Wang, Li, Jian, Hui, Zhu, Jing, Xiao, Yuanyuan, Tan, Mengyu, Xue, Jiaming, Yang, Fan, Liang, Weibo
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2022
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8866868/ https://www.ncbi.nlm.nih.gov/pubmed/35222521 http://dx.doi.org/10.3389/fgene.2021.800598

Ejemplares similares

Noninvasive prenatal paternity testing by means of SNP‐based targeted sequencing
por: Tam, Jacqueline Chor Wing, et al.
Publicado: (2020)

Evaluation of a Custom SNP Panel for Identifying and Rectifying of Misjudged Paternity in Deficiency Cases
por: Chang, Liao, et al.
Publicado: (2021)

Noninvasive Prenatal Paternity Testing with a Combination of Well-Established SNP and STR Markers Using Massively Parallel Sequencing
por: Shen, Xuefeng, et al.
Publicado: (2021)

A Novel SNP-STR System Based on a Capillary Electrophoresis Platform
por: Jian, Hui, et al.
Publicado: (2021)

Corrigendum: A novel SNP-STR system based on a capillary electrophoresis platform
por: Jian, Hui, et al.
Publicado: (2022)

Clinical Utility of SNP Array Analysis in Prenatal Diagnosis: A Cohort Study of 5000 Pregnancies
por: Xiang, Jingjing, et al.
Publicado: (2020)

SNP–SNP Interactions of Surfactant Protein Genes in Persistent Respiratory Morbidity Susceptibility in Previously Healthy Children
por: Gandhi, Chintan K., et al.
Publicado: (2022)

Examining SNP-SNP interactions and risk of clinical outcomes in colorectal cancer using multifactor dimensionality reduction based methods
por: Curtis, Aaron, et al.
Publicado: (2022)

SNPMap—An integrated visual SNP interpretation tool
por: Liu, Miaosen, et al.
Publicado: (2022)

SNP Data Quality Control in a National Beef and Dairy Cattle System and Highly Accurate SNP Based Parentage Verification and Identification
por: McClure, Matthew C., et al.
Publicado: (2018)

SNP imputation bias reduces effect size determination
por: Khankhanian, Pouya, et al.
Publicado: (2015)

Machine Learning SNP Based Prediction for Precision Medicine
por: Ho, Daniel Sik Wai, et al.
Publicado: (2019)

Meta-Analysis of SNP-Environment Interaction With Overlapping Data
por: Jin, Qinqin, et al.
Publicado: (2020)

Importance of SNP Dependency Correction and Association Integration for Gene Set Analysis in Genome-Wide Association Studies
por: Marczyk, Michal, et al.
Publicado: (2021)

Performance of SNP barcodes to determine genetic diversity and population structure of Plasmodium falciparum in Africa
por: Argyropoulos, Dionne C., et al.
Publicado: (2023)

snpXplorer: a web application to explore human SNP-associations and annotate SNP-sets
por: Tesi, Niccolo, et al.
Publicado: (2021)

GVCHAP: A Computing Pipeline for Genomic Prediction and Variance Component Estimation Using Haplotypes and SNP Markers
por: Prakapenka, Dzianis, et al.
Publicado: (2020)

Considering strategies for SNP selection in genetic and polygenic risk scores
por: St.-Pierre, Julien, et al.
Publicado: (2022)

Paternal Tobacco Smoke Correlated to Offspring Asthma and Prenatal Epigenetic Programming
por: Wu, Chih-Chiang, et al.
Publicado: (2019)

Identification of a Diverse Core Set Panel of Rice From the East Coast Region of India Using SNP Markers
por: Choudhury, Debjani Roy, et al.
Publicado: (2021)

SNP-SNP interactions in breast cancer susceptibility
por: Onay, Venüs Ümmiye, et al.
Publicado: (2006)

Imputation of Microsatellite Alleles from Dense SNP Genotypes for Parental Verification
por: McClure, Matthew, et al.
Publicado: (2012)

Evaluation of SNP Genotyping in Alpacas Using the Bovine HD Genotyping Beadchip
por: More, Manuel, et al.
Publicado: (2019)

Genome-Wide SNP Discovery in Indigenous Cattle Breeds of South Africa
por: Zwane, Avhashoni A., et al.
Publicado: (2019)

Informatics-based, highly accurate, noninvasive prenatal paternity testing
por: Ryan, Allison, et al.
Publicado: (2013)

Effective Identification of Maternal Malignancies in Pregnancies Undergoing Noninvasive Prenatal Testing
por: Li, Jia, et al.
Publicado: (2022)

Genome-Wide Detection of CNVs and Association With Body Weight in Sheep Based on 600K SNP Arrays
por: Wang, Zhipeng, et al.
Publicado: (2020)

SNP-based bulk segregant analysis revealed disease resistance QTLs associated with northern corn leaf blight in maize
por: Zhai, Ruining, et al.
Publicado: (2022)

SNP-PRAGE: SNP-based parametric robust analysis of gene set enrichment
por: Lee, Jaehoon, et al.
Publicado: (2011)

Evaluation of ten SNP Markers for Human Identification and Paternity Analysis in Persian Population
por: Habibi, Sajad, et al.
Publicado: (2019)

Selection and evaluation of bi-allelic autosomal SNP markers for paternity testing in Koreans
por: Bae, Soyeon, et al.
Publicado: (2021)

Bayesian Methods for Multivariate Modeling of Pleiotropic SNP Associations and Genetic Risk Prediction
por: Hartley, Stephen W., et al.
Publicado: (2012)

Family-Based Multi-SNP X Chromosome Analysis Using Parent Information
por: Wise, Alison S., et al.
Publicado: (2016)

FeatSNP: An Interactive Database for Brain-Specific Epigenetic Annotation of Human SNPs
por: Ma, Chun-yu, et al.
Publicado: (2019)

SNP-Flankplus: SNP ID-centric retrieval for SNP flanking sequences
por: Yang, Cheng-Hong, et al.
Publicado: (2008)

Performance of noninvasive prenatal testing for twin pregnancies in South China
por: Wang, Dongmei, et al.
Publicado: (2023)

Patient attitudes and preferences about expanded noninvasive prenatal testing
por: Dubois, Marie-Line, et al.
Publicado: (2023)

Noninvasive prenatal paternity determination using microhaplotypes: a pilot study
por: Wang, Jaqueline Yu Ting, et al.
Publicado: (2020)

Early noninvasive prenatal paternity testing by targeted fetal DNA analysis
por: Damour, Géraldine, et al.
Publicado: (2023)

Reducing Bias of Allele Frequency Estimates by Modeling SNP Genotype Data with Informative Missingness
por: Lin, Wan-Yu, et al.
Publicado: (2012)

Cannot write session to /tmp/vufind_sessions/sess_f40e3ppv52mqj68msjh6hd2m3g