Rapid Discovery of De Novo Deleterious Mutations in Cattle Enhances the Value of Livestock as Model Species
Published 2017 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Rapid Discovery of De Novo Deleterious Mutations in Cattle Enhances the Value of Livestock as Model Species
Authors
Keywords
-
Journal
Scientific Reports
Volume 7, Issue 1, Pages -
Publisher
Springer Nature
Online
2017-09-07
DOI
10.1038/s41598-017-11523-3
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Copa Syndrome: a Novel Autosomal Dominant Immune Dysregulatory Disease
- (2016) Timothy J. Vece et al. JOURNAL OF CLINICAL IMMUNOLOGY
- Enrichr: a comprehensive gene set enrichment analysis web server 2016 update
- (2016) Maxim V. Kuleshov et al. NUCLEIC ACIDS RESEARCH
- The harmonizome: a collection of processed datasets gathered to serve and mine knowledge about genes and proteins
- (2016) Andrew D. Rouillard et al. Database-The Journal of Biological Databases and Curation
- Interleukin-33 in Tissue Homeostasis, Injury, and Inflammation
- (2015) Ari B. Molofsky et al. IMMUNITY
- COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis
- (2015) Levi B Watkin et al. NATURE GENETICS
- Dominant Red Coat Color in Holstein Cattle Is Associated with a Missense Mutation in the Coatomer Protein Complex, Subunit Alpha (COPA) Gene
- (2015) Ben Dorshorst et al. PLoS One
- A new approach for efficient genotype imputation using information from relatives
- (2014) Mehdi Sargolzaei et al. BMC GENOMICS
- Whole-genome sequencing of 234 bulls facilitates mapping of monogenic and complex traits in cattle
- (2014) Hans D Daetwyler et al. NATURE GENETICS
- Family history and clefting as major criteria for CHARGE syndrome
- (2013) Susan Starling Hughes et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Molecular consequences of animal breeding
- (2013) Leif Andersson CURRENT OPINION IN GENETICS & DEVELOPMENT
- NFIB is a governor of epithelial–melanocyte stem cell behaviour in a shared niche
- (2013) Chiung-Ying Chang et al. NATURE
- The ectodysplasin pathway: from diseases to adaptations
- (2013) Alexa Sadier et al. TRENDS IN GENETICS
- DELLY: structural variant discovery by integrated paired-end and split-read analysis
- (2012) T. Rausch et al. BIOINFORMATICS
- Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration
- (2012) H. Thorvaldsdottir et al. BRIEFINGS IN BIOINFORMATICS
- Molecular Basis for Recognition of Dilysine Trafficking Motifs by COPI
- (2012) Lauren P. Jackson et al. DEVELOPMENTAL CELL
- Novel and recurrent non-truncating mutations of the MITF basic domain: genotypic and phenotypic variations in Waardenburg and Tietz syndromes
- (2012) Sandy Léger et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- GATA believe it: new essential regulators of pancreas development
- (2012) Santiago Rodríguez-Seguí et al. JOURNAL OF CLINICAL INVESTIGATION
- Genomic selection in French dairy cattle
- (2012) D. Boichard et al. Animal Production Science
- Mutations in MITF and PAX3 Cause “Splashed White” and Other White Spotting Phenotypes in Horses
- (2012) Regula Hauswirth et al. PLoS Genetics
- Interleukin-25: Key Regulator of Inflammatory and Autoimmune Diseases
- (2011) David Saadoun et al. CURRENT PHARMACEUTICAL DESIGN
- A Missense Mutation in the Death Domain of EDAR Abolishes the Interaction with EDARADD and Underlies Hypohidrotic Ectodermal Dysplasia
- (2011) Yukiko Masui et al. DERMATOLOGY
- A MITF Mutation Associated with a Dominant White Phenotype and Bilateral Deafness in German Fleckvieh Cattle
- (2011) Ute Philipp et al. PLoS One
- ChEA: transcription factor regulation inferred from integrating genome-wide ChIP-X experiments
- (2010) Alexander Lachmann et al. BIOINFORMATICS
- Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor
- (2010) William McLaren et al. BIOINFORMATICS
- The role of type I collagen in the regulation of the osteoblast phenotype
- (2010) Songtao Shi et al. JOURNAL OF BONE AND MINERAL RESEARCH
- CHD7 cooperates with PBAF to control multipotent neural crest formation
- (2010) Ruchi Bajpai et al. NATURE
- Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads
- (2009) K. Ye et al. BIOINFORMATICS
- The Sequence Alignment/Map format and SAMtools
- (2009) H. Li et al. BIOINFORMATICS
- Fast and accurate short read alignment with Burrows-Wheeler transform
- (2009) H. Li et al. BIOINFORMATICS
- A familial CHARGE syndrome with a CHD7 nonsense mutation and new clinical features
- (2008) Pia E. Vuorela et al. CLINICAL DYSMORPHOLOGY
- Pulmonary hypoplasia in the connective tissue growth factor (Ctgf) null mouse
- (2008) Mark Baguma-Nibasheka et al. DEVELOPMENTAL DYNAMICS
- Ectopic SOX9 Mediates Extracellular Matrix Deposition Characteristic of Organ Fibrosis
- (2008) Karen Piper Hanley et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- N-cadherin haploinsufficiency affects cardiac gap junctions and arrhythmic susceptibility
- (2008) Jifen Li et al. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY
- Highly effective SNP-based association mapping and management of recessive defects in livestock
- (2008) Carole Charlier et al. NATURE GENETICS
Become a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get StartedAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started