标题
Predicting the impact of non-coding variants on DNA methylation
作者
关键词
-
出版物
NUCLEIC ACIDS RESEARCH
Volume 45, Issue 11, Pages e99-e99
出版商
Oxford University Press (OUP)
发表日期
2017-03-14
DOI
10.1093/nar/gkx177
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Convolutional neural network architectures for predicting DNA–protein binding
- (2016) Haoyang Zeng et al. BIOINFORMATICS
- Basset: learning the regulatory code of the accessible genome with deep convolutional neural networks
- (2016) David R. Kelley et al. GENOME RESEARCH
- Predicting CpG methylation levels by integrating Infinium HumanMethylation450 BeadChip array data
- (2016) Shicai Fan et al. GENOMICS
- A pooling-based approach to mapping genetic variants associated with DNA methylation
- (2015) Irene M. Kaplow et al. GENOME RESEARCH
- Predicting the sequence specificities of DNA- and RNA-binding proteins by deep learning
- (2015) Babak Alipanahi et al. NATURE BIOTECHNOLOGY
- A method to predict the impact of regulatory variants from DNA sequence
- (2015) Dongwon Lee et al. NATURE GENETICS
- Predicting effects of noncoding variants with deep learning–based sequence model
- (2015) Jian Zhou et al. NATURE METHODS
- Developmental enhancers revealed by extensive DNA methylome maps of zebrafish early embryos
- (2015) Hyung Joo Lee et al. Nature Communications
- Predicting genome-wide DNA methylation using methylation marks, genomic position, and DNA regulatory elements
- (2015) Weiwei Zhang et al. GENOME BIOLOGY
- Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases
- (2014) Alexander Gusev et al. AMERICAN JOURNAL OF HUMAN GENETICS
- GRASP: analysis of genotype-phenotype results from 1390 genome-wide association studies and corresponding open access database
- (2014) R. Leslie et al. BIOINFORMATICS
- Determination and Inference of Eukaryotic Transcription Factor Sequence Specificity
- (2014) Matthew T. Weirauch et al. CELL
- A general framework for estimating the relative pathogenicity of human genetic variants
- (2014) Martin Kircher et al. NATURE GENETICS
- Functional annotation of noncoding sequence variants
- (2014) Graham R S Ritchie et al. NATURE METHODS
- Genome Wide Association Study of Fetal Hemoglobin in Sickle Cell Anemia in Tanzania
- (2014) Siana Nkya Mtatiro et al. PLoS One
- Seven new loci associated with age-related macular degeneration
- (2013) Lars G Fritsche et al. NATURE GENETICS
- The NHGRI GWAS Catalog, a curated resource of SNP-trait associations
- (2013) Danielle Welter et al. NUCLEIC ACIDS RESEARCH
- An Erythroid Enhancer of BCL11A Subject to Genetic Variation Determines Fetal Hemoglobin Level
- (2013) D. E. Bauer et al. SCIENCE
- Analysing and interpreting DNA methylation data
- (2012) Christoph Bock NATURE REVIEWS GENETICS
- Systematic Localization of Common Disease-Associated Variation in Regulatory DNA
- (2012) M. T. Maurano et al. SCIENCE
- Genome-Wide Association for Abdominal Subcutaneous and Visceral Adipose Reveals a Novel Locus for Visceral Fat in Women
- (2012) Caroline S. Fox et al. PLoS Genetics
- Genomic Imprinting: A Mammalian Epigenetic Discovery Model
- (2011) Denise P. Barlow Annual Review of Genetics
- A fast, lock-free approach for efficient parallel counting of occurrences of k-mers
- (2011) Guillaume Marçais et al. BIOINFORMATICS
- Prediction of methylation CpGs and their methylation degrees in human DNA sequences
- (2011) Xuan Zhou et al. COMPUTERS IN BIOLOGY AND MEDICINE
- Dnmt3/transcription factor interactions as crucial players in targeted DNA methylation
- (2010) Eric Hervouet et al. Epigenetics
- From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus
- (2010) Kiran Musunuru et al. NATURE
- Epigenetic modifications in pluripotent and differentiated cells
- (2010) Alexander Meissner NATURE BIOTECHNOLOGY
- Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
- (2009) L. A. Hindorff et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Common variants at 30 loci contribute to polygenic dyslipidemia
- (2008) Sekar Kathiresan et al. NATURE GENETICS
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started