Cargando…

Beware of risk for increased false positive rates in genome-wide association studies for phenotypic variability

Detalles Bibliográficos
Autores principales:	Shen, Xia, Carlborg, Örjan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2013
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659368/ https://www.ncbi.nlm.nih.gov/pubmed/23734164 http://dx.doi.org/10.3389/fgene.2013.00093

Ejemplares similares

Beware of False “Type Strain” Genome Sequences
por: Salvà-Serra, Francisco, et al.
Publicado: (2019)

Generation of a Multi-Locus Chicken Introgression Line to Study the Effects of Genetic Interactions on Metabolic Phenotypes in Chickens
por: Ek, Weronica, et al.
Publicado: (2012)

Beware of AI programs bearing false gifts
por: Field, Richard E
Publicado: (2023)

PASE: a novel method for functional prediction of amino acid substitutions based on physicochemical properties
por: Li, Xidan, et al.
Publicado: (2013)

Correcting for Population Stratification Reduces False Positive and False Negative Results in Joint Analyses of Host and Pathogen Genomes
por: Naret, Olivier, et al.
Publicado: (2018)

Hierarchical likelihood opens a new way of estimating genetic values using genome-wide dense marker maps
por: Shen, Xia, et al.
Publicado: (2011)

Genome-wide association studies of polygenic risk score-derived phenotypes may lead to inflated false positive rates
por: Uffelmann, Emil, et al.
Publicado: (2023)

A Genome-Wide Association Analysis Reveals Epistatic Cancellation of Additive Genetic Variance for Root Length in Arabidopsis thaliana
por: Lachowiec, Jennifer, et al.
Publicado: (2015)

Reply to: Genome-wide association studies of polygenic risk score-derived phenotypes may lead to inflated false positive rates
por: Guerreiro, Rita, et al.
Publicado: (2023)

SNP detection and prediction of variability between chicken lines using genome resequencing of DNA pools
por: Marklund, Stefan, et al.
Publicado: (2010)

Balancing false positives and false negatives for the detection of differential expression in malignancies
por: De Smet, F, et al.
Publicado: (2004)

Lateral position… beware!
por: Dhansura, Tasneem, et al.
Publicado: (2016)

Surveillance Screening in Li-Fraumeni Syndrome: Raising Awareness of False Positives
por: Kumar, Prerna, et al.
Publicado: (2018)

Genome-Wide Effects of Long-Term Divergent Selection
por: Johansson, Anna M., et al.
Publicado: (2010)

Genome-Wide Detection of Copy Number Variations and Their Association With Distinct Phenotypes in the World’s Sheep
por: Salehian-Dehkordi, Hosein, et al.
Publicado: (2021)

Identification of candidate genes and mutations in QTL regions for chicken growth using bioinformatic analysis of NGS and SNP-chip data
por: Ahsan, Muhammad, et al.
Publicado: (2013)

False ground-glass opacity and suspicion of COVID-19, beware of the technique for performing the CT
por: Niang, Ibrahima, et al.
Publicado: (2020)

Natural CMT2 Variation Is Associated With Genome-Wide Methylation Changes and Temperature Seasonality
por: Shen, Xia, et al.
Publicado: (2014)

Issues with data transformation in genome-wide association studies for phenotypic variability
por: Shen, Xia, et al.
Publicado: (2013)

Whole-genome selective sweep analyses identifies the region and candidate gene associated with white earlobe color in Mediterranean chickens
por: Guo, Ying, et al.
Publicado: (2023)

A genome-wide association study using international breeding-evaluation data identifies major loci affecting production traits and stature in the Brown Swiss cattle breed
por: Guo, Jiazhong, et al.
Publicado: (2012)

Sequencing Shorter cfDNA Fragments Decreases the False Negative Rate of Non-invasive Prenatal Testing
por: Xue, Ying, et al.
Publicado: (2020)

Clinical Implications of Human Population Differences in Genome-Wide Rates of Functional Genotypes
por: Torkamani, Ali, et al.
Publicado: (2012)

Exploring the potential benefits of stratified false discovery rates for region-based testing of association with rare genetic variation
por: Xu, ChangJiang, et al.
Publicado: (2014)

Comparison of false-discovery rate for genome-wide and fine mapping regions
por: Tabangin, Meredith E, et al.
Publicado: (2007)

Controlled Reduction of Genomic Heterozygosity in an Industrial Yeast Strain Reveals Wide Cryptic Phenotypic Variation
por: Sampaio, Nadia M. V., et al.
Publicado: (2019)

Phenotype Prediction and Genome-Wide Association Study Using Deep Convolutional Neural Network of Soybean
por: Liu, Yang, et al.
Publicado: (2019)

Corrigendum: Exploring the potential benefits of stratified false discovery rates for region-based testing of association with rare genetic variation
por: Greenwood, Celia M. T.
Publicado: (2014)

Data Integration Methods for Phenotype Harmonization in Multi-Cohort Genome-Wide Association Studies With Behavioral Outcomes
por: Luningham, Justin M., et al.
Publicado: (2019)

Genome-Wide Association Study and Transcriptome Differential Expression Analysis of the Feather Rate in Shouguang Chickens
por: Liu, Xiayi, et al.
Publicado: (2020)

Including Phenotypic Causal Networks in Genome-Wide Association Studies Using Mixed Effects Structural Equation Models
por: Momen, Mehdi, et al.
Publicado: (2018)

Magnesium- a Forgotten Element: Phenotypic Variation and Genome Wide Association Study in Turkish Common Bean Germplasm
por: Baloch, Faheem Shehzad, et al.
Publicado: (2022)

The genetic architecture of blood pressure variability: A genome‐wide association study of 9370 participants from UK Biobank
por: Jia, Pingping, et al.
Publicado: (2022)

False discovery rate control in genome-wide association studies with population structure
por: Sesia, Matteo, et al.
Publicado: (2021)

Comparison of analyses of the QTLMAS XII common dataset. II: genome-wide association and fine mapping
por: Crooks, Lucy, et al.
Publicado: (2009)

Beware the Borg
por: Wells, William A.
Publicado: (2001)

Hackers beware
por: Cole, Eric
Publicado: (2002)

Beware the algorithm
por: van Endert, Peter
Publicado: (2021)

The aging-disease false dichotomy: understanding senescence as pathology
por: Gems, David
Publicado: (2015)

A general and efficient method for estimating continuous IBD functions for use in genome scans for QTL
por: Besnier, Francois, et al.
Publicado: (2007)

Cannot write session to /tmp/vufind_sessions/sess_r0dt81oe9qn8n1gkvpo0ehuv9e