Characterization of parent-of-origin methylation using the Illumina Infinium MethylationEPIC array platform
出版年份 2018 全文链接
标题
Characterization of parent-of-origin methylation using the Illumina Infinium MethylationEPIC array platform
作者
关键词
-
出版物
Epigenomics
Volume 10, Issue 7, Pages 941-954
出版商
Future Medicine Ltd
发表日期
2018-07-02
DOI
10.2217/epi-2017-0172
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Profiling of oxBS-450K 5-hydroxymethylcytosine in human placenta and brain reveals enrichment at imprinted loci
- (2018) Jose Ramon Hernandez Mora et al. Epigenetics
- Recommendations for a nomenclature system for reporting methylation aberrations in imprinted domains
- (2018) David Monk et al. Epigenetics
- Copy number rather than epigenetic alterations are the major dictator of imprinted methylation in tumors
- (2017) Alex Martin-Trujillo et al. Nature Communications
- DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome
- (2016) Ricky S. Joshi et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Recent Advances in Imprinting Disorders
- (2016) L. Soellner et al. CLINICAL GENETICS
- Genome-wide methylation analysis of retrocopy-associated CpG islands and their genomic environment
- (2016) Katrin Grothaus et al. Epigenetics
- Causes and Consequences of Multi-Locus Imprinting Disturbances in Humans
- (2016) Marta Sanchez-Delgado et al. TRENDS IN GENETICS
- Validation of a DNA methylation microarray for 850,000 CpG sites of the human genome enriched in enhancer sequences
- (2016) Sebastian Moran et al. Epigenomics
- Human Oocyte-Derived Methylation Differences Persist in the Placenta Revealing Widespread Transient Imprinting
- (2016) Marta Sanchez-Delgado et al. PLoS Genetics
- Evolutionary Transition of Promoter and Gene Body DNA Methylation across Invertebrate–Vertebrate Boundary
- (2015) Thomas E. Keller et al. MOLECULAR BIOLOGY AND EVOLUTION
- Exploration of hydroxymethylation in Kagami-Ogata syndrome caused by hypermethylation of imprinting control regions
- (2015) Keiko Matsubara et al. Clinical Epigenetics
- A statistical method for single sample analysis of HumanMethylation450 array data: genome-wide methylation analysis of patients with imprinting disorders
- (2015) Faisal I Rezwan et al. Clinical Epigenetics
- Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment
- (2014) F. Court et al. GENOME RESEARCH
- Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes
- (2014) Louise E Docherty et al. JOURNAL OF MEDICAL GENETICS
- Epigenetic and transcriptional features of the novel human imprinted lncRNAGPR1ASsuggest it is a functional ortholog to mouseZdbf2linc
- (2013) Hisato Kobayashi et al. Epigenetics
- Differentially methylated regions in maternal and paternal uniparental disomy for chromosome 7
- (2013) Katariina Hannula-Jouppi et al. Epigenetics
- RNAs of the human chromosome 15q11-q13 imprinted region
- (2012) Stormy J. Chamberlain Wiley Interdisciplinary Reviews-RNA
- Bismark: a flexible aligner and methylation caller for Bisulfite-Seq applications
- (2011) Felix Krueger et al. BIOINFORMATICS
- Methylation screening of reciprocal genome-wide UPDs identifies novel human-specific imprinted genes†
- (2011) Kazuhiko Nakabayashi et al. HUMAN MOLECULAR GENETICS
- Androgenetic/biparental mosaicism in a girl with Beckwith–Wiedemann syndrome-like and upd(14)pat-like phenotypes
- (2010) Kazuki Yamazawa et al. JOURNAL OF HUMAN GENETICS
- Constitutional mosaic genome-wide uniparental disomy due to diploidisation: an unusual cancer-predisposing mechanism
- (2010) V. Romanelli et al. JOURNAL OF MEDICAL GENETICS
- Parthenogenetic chimaerism/mosaicism with a Silver-Russell syndrome-like phenotype
- (2010) K. Yamazawa et al. JOURNAL OF MEDICAL GENETICS
- Genomic imprinting in germ cells: imprints are under control
- (2010) Philippe Arnaud REPRODUCTION
- The Sequence Alignment/Map format and SAMtools
- (2009) H. Li et al. BIOINFORMATICS
- Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57
- (2008) Deborah J G Mackay et al. NATURE GENETICS
- QUMA: quantification tool for methylation analysis
- (2008) Y. Kumaki et al. NUCLEIC ACIDS RESEARCH
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