Cargando…

Burden tests can be used to map causal genes for a simple metabolic trait in an exome‐sequenced polyploid mutant population

Detalles Bibliográficos
Autores principales:	Menard, Guillaume N., Eastmond, Peter J.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2022
Materias:	Brief Communications
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9491453/ https://www.ncbi.nlm.nih.gov/pubmed/35810345 http://dx.doi.org/10.1111/pbi.13890

Ejemplares similares

Mapping causal mutations by exome sequencing in a wheat TILLING population: a tall mutant case study
por: Mo, Youngjun, et al.
Publicado: (2017)

Sequence-Based Mapping of the Polyploid Wheat Genome
por: Saintenac, Cyrille, et al.
Publicado: (2013)

Polyploid engineering by increasing mutant gene dosage in yeasts
por: Fukuda, Nobuo, et al.
Publicado: (2020)

Dissecting Key Adaptation Traits in the Polyploid Perennial Medicago sativa Using GBS-SNP Mapping
por: Adhikari, Laxman, et al.
Publicado: (2018)

Whole‐Exome Sequencing Study of Extreme Phenotypes of NAFLD
por: Kleinstein, Sarah E., et al.
Publicado: (2018)

Whole exome sequencing may be insufficient to cover the causality spectrum of rhabdomyolysis
por: Finsterer, Josef, et al.
Publicado: (2018)

Exome Sequencing as a Diagnostic Tool for Pediatric-Onset Ataxia
por: Sawyer, Sarah L, et al.
Publicado: (2014)

PERGOLA: fast and deterministic linkage mapping of polyploids
por: Grandke, Fabian, et al.
Publicado: (2017)

Nucleotide polymorphism and copy number variant detection using exome capture and next-generation sequencing in the polyploid grass Panicum virgatum
por: Evans, Joseph, et al.
Publicado: (2014)

Evaluation of Exome Sequencing to Estimate Tumor Burden in Plasma
por: Klevebring, Daniel, et al.
Publicado: (2014)

Lifting the lid on unborn lethal Mendelian phenotypes through exome sequencing
por: Shamseldin, Hanan E., et al.
Publicado: (2013)

Exome-Sequence Analyses of Four Multi-Incident Multiple Sclerosis Families
por: Zrzavy, Tobias, et al.
Publicado: (2020)

Whole‐exome and HLA sequencing in Febrile infection‐related epilepsy syndrome
por: Helbig, Ingo, et al.
Publicado: (2020)

Whole‐exome sequencing analysis of juvenile papillomatosis and coexisting breast carcinoma
por: D'Alfonso, Timothy M, et al.
Publicado: (2020)

Functional trait divergence and trait plasticity confer polyploid advantage in heterogeneous environments
por: Wei, Na, et al.
Publicado: (2018)

Identification of potential genetic causal variants for rheumatoid arthritis by whole-exome sequencing
por: Li, Ying, et al.
Publicado: (2017)

Identification of potential causal variants for premature ovarian failure by whole exome sequencing
por: Jin, Haengun, et al.
Publicado: (2020)

Meiosis in Polyploids and Implications for Genetic Mapping: A Review
por: Soares, Nina Reis, et al.
Publicado: (2021)

Multiallelic models for QTL mapping in diverse polyploid populations
por: Thérèse Navarro, Alejandro, et al.
Publicado: (2022)

Platform comparison of detecting copy number variants with microarrays and whole-exome sequencing
por: de Ligt, Joep, et al.
Publicado: (2014)

Accurate detection of clinically relevant uniparental disomy from exome sequencing data
por: Yauy, Kevin, et al.
Publicado: (2019)

Human Liver Cell Trafficking Mutants: Characterization and Whole Exome Sequencing
por: Yuan, Fei, et al.
Publicado: (2014)

A native promoter–gene fusion created by CRISPR/Cas9‐mediated genomic deletion offers a transgene‐free method to drive oil accumulation in leaves
por: Bhunia, Rupam Kumar, et al.
Publicado: (2022)

Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing
por: Ammar-Khodja, Fatima, et al.
Publicado: (2015)

Complications of whole-exome sequencing for causal gene discovery in primary platelet secretion defects
por: Gorski, Marcin M., et al.
Publicado: (2019)

Gene-based multiple trait analysis for exome sequencing data
por: Zhao, Jingyuan, et al.
Publicado: (2011)

Utility of Clinical Exome Sequencing in Dystonia: A Single-Center Study From India
por: Holla, Vikram Venkappayya, et al.
Publicado: (2022)

An Exome-seq Based Tool for Mapping and Selection of Candidate Genes in Maize Deletion Mutants
por: Jia, Shangang, et al.
Publicado: (2018)

Mapping‐by‐sequencing in complex polyploid genomes using genic sequence capture: a case study to map yellow rust resistance in hexaploid wheat
por: Gardiner, Laura‐Jayne, et al.
Publicado: (2016)

A causal inference and Bayesian optimisation framework for modelling multi-trait relationships—Proof-of-concept using Brassica napus seed yield under controlled conditions
por: Calderwood, Alexander, et al.
Publicado: (2023)

Applying the latest advances in genomics and phenomics for trait discovery in polyploid wheat
por: Borrill, Philippa, et al.
Publicado: (2018)

Life‐history traits of the Whiting polyploid line of the parasitoid Nasonia vitripennis
por: Leung, Kelley, et al.
Publicado: (2019)

Engineering homoeologs provide a fine scale for quantitative traits in polyploid
por: Lee, Eun Song, et al.
Publicado: (2023)

Identification of Two Cases of Ciliopathy-Associated Diabetes and Their Mutation Analysis Using Whole Exome Sequencing
por: Kim, Min Kyeong, et al.
Publicado: (2015)

Whole-exome sequencing for a more accurate diagnosis of intraductal papillary neoplasms of the bile duct
por: Matsumori, Tomoaki, et al.
Publicado: (2021)

ABNORMAL CYCLE PHASE DURATIONS IN POLYPLOID CELLS OR CELLS WITH IRREGULAR MITOSIS IN A HELA CELL POPULATION
por: Firket, H., et al.
Publicado: (1970)

A domestic cat whole exome sequencing resource for trait discovery
por: Rodney, Alana R., et al.
Publicado: (2021)

A Population of Deletion Mutants and an Integrated Mapping and Exome-seq Pipeline for Gene Discovery in Maize
por: Jia, Shangang, et al.
Publicado: (2016)

Whole-exome sequencing exploration of acquired uniparental disomies in B-cell precursor acute lymphoblastic leukemia
por: Lundin-Ström, Kristina B., et al.
Publicado: (2018)

Identification of Maturity-Onset Diabetes of the Young Caused by Glucokinase Mutations Detected Using Whole-Exome Sequencing
por: Cho, Eun-Hee, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_7cnpg3vnsi93htbfs0pm1ee63u