A Transcription Start Site Map in Human Pancreatic Islets Reveals Functional Regulatory Signatures
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Stephen C. J. Parker | J. Kitzman | F. Collins | M. Erdos | N. Narisu | M. Stitzel | Peter Orchard | Arushi Varshney | R. D. Albanus | Yasuhiro Kyono | V. Elangovan | Collin Wang | P. Orchard | R. Albanus | Narisu Narisu | Ricardo D’Oliveira Albanus
[1] Stephen C. J. Parker,et al. Genetic variant effects on gene expression in human pancreatic islets and their implications for T2D , 2020, Nature Communications.
[2] Stephen C. J. Parker,et al. Single-cell ATAC-Seq in human pancreatic islets and deep learning upscaling of rare cells reveals cell-specific type 2 diabetes regulatory signatures , 2019, Molecular metabolism.
[3] Inês Cebola. Pancreatic Islet Transcriptional Enhancers and Diabetes , 2019, Current Diabetes Reports.
[4] Stephen C. J. Parker,et al. Single-cell ATAC-Seq in human pancreatic islets and deep learning upscaling of rare cells reveals cell-specific type 2 diabetes regulatory signatures , 2019, bioRxiv.
[5] Cosmas D. Arnold,et al. STARR‐seq and UMI‐STARR‐seq: Assessing Enhancer Activities for Genome‐Wide‐, High‐, and Low‐Complexity Candidate Libraries , 2019, Current protocols in molecular biology.
[6] J. Kere,et al. NET-CAGE characterizes the dynamics and topology of human transcribed cis-regulatory elements , 2019, Nature Genetics.
[7] David Torrents,et al. Human pancreatic islet three-dimensional chromatin architecture provides insights into the genetics of type 2 diabetes , 2019, Nature Genetics.
[8] William W. Greenwald,et al. Subtle changes in chromatin loop contact propensity are associated with differential gene regulation and expression , 2019, Nature Communications.
[9] E. Birney,et al. GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signals , 2019, Nature Genetics.
[10] Fabian J. Theis,et al. MPRAnalyze: statistical framework for massively parallel reporter assays , 2019, bioRxiv.
[11] Stephen C. J. Parker,et al. Cell Specificity of Human Regulatory Annotations and Their Genetic Effects on Gene Expression , 2018, Genetics.
[12] Sarah M. Goggin,et al. High-resolution genome-wide functional dissection of transcriptional regulatory regions and nucleotides in human , 2018, Nature Communications.
[13] Anthony J. Payne,et al. Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps , 2018, Nature Genetics.
[14] J. Kere,et al. Characterization of the human RFX transcription factor family by regulatory and target gene analysis , 2018, BMC Genomics.
[15] I. Schor,et al. The degree of enhancer or promoter activity is reflected by the levels and directionality of eRNA transcription , 2018, Genes & development.
[16] Nicola J. Rinaldi,et al. Genetic effects on gene expression across human tissues , 2017, Nature.
[17] Kyle J. Gaulton,et al. Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci , 2017, bioRxiv.
[18] Stephen C. J. Parker,et al. A Type 2 Diabetes–Associated Functional Regulatory Variant in a Pancreatic Islet Enhancer at the ADCY5 Locus , 2017, Diabetes.
[19] Laura J. Scott,et al. Genetic regulatory signatures underlying islet gene expression and type 2 diabetes , 2017, Proceedings of the National Academy of Sciences.
[20] R. Agami,et al. GRO-seq, A Tool for Identification of Transcripts Regulating Gene Expression. , 2017, Methods in molecular biology.
[21] T. Mikkelsen,et al. Genome-scale high-resolution mapping of activating and repressive nucleotides in regulatory regions , 2016, Nature Biotechnology.
[22] J. van Helden,et al. RSAT matrix-clustering: dynamic exploration and redundancy reduction of transcription factor binding motif collections , 2016, bioRxiv.
[23] Laura J. Scott,et al. The genetic regulatory signature of type 2 diabetes in human skeletal muscle , 2016, Nature Communications.
[24] P. Unger,et al. ZBTB16: a novel sensitive and specific biomarker for yolk sac tumor , 2016, Modern Pathology.
[25] David J. Arenillas,et al. JASPAR 2016: a major expansion and update of the open-access database of transcription factor binding profiles , 2015, Nucleic Acids Res..
[26] Mark I. McCarthy,et al. Transcript Expression Data from Human Islets Links Regulatory Signals from Genome-Wide Association Studies for Type 2 Diabetes and Glycemic Traits to Their Downstream Effectors , 2015, PLoS genetics.
[27] Yasuyuki Ohkawa,et al. Agplus: a Rapid and Flexible Tool for Aggregation Plots , 2015, Bioinform..
[28] Yakir A Reshef,et al. Partitioning heritability by functional annotation using genome-wide association summary statistics , 2015, Nature Genetics.
[29] Stephen Hartley,et al. QoRTs: a comprehensive toolset for quality control and data processing of RNA-Seq experiments , 2015, BMC Bioinformatics.
[30] Stephen C. J. Parker,et al. Motif signatures in stretch enhancers are enriched for disease-associated genetic variants , 2015, Epigenetics & Chromatin.
[31] M. Andersen,et al. CNC-bZIP protein Nrf1-dependent regulation of glucose-stimulated insulin secretion. , 2015, Antioxidants & redox signaling.
[32] Michael Q. Zhang,et al. Integrative analysis of 111 reference human epigenomes , 2015, Nature.
[33] Guillaume J. Filion,et al. Starcode: sequence clustering based on all-pairs search , 2015, Bioinform..
[34] André L. Martins,et al. Analysis of nascent RNA identifies a unified architecture of initiation regions at mammalian promoters and enhancers , 2014, Nature Genetics.
[35] Han Xu,et al. Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. , 2014, American journal of human genetics.
[36] L. Groop,et al. Global genomic and transcriptomic analysis of human pancreatic islets reveals novel genes influencing glucose metabolism , 2014, Proceedings of the National Academy of Sciences.
[37] Paul Theodor Pyl,et al. HTSeq—a Python framework to work with high-throughput sequencing data , 2014, bioRxiv.
[38] C. Spencer,et al. Biological Insights From 108 Schizophrenia-Associated Genetic Loci , 2014, Nature.
[39] T. Meehan,et al. An atlas of active enhancers across human cell types and tissues , 2014, Nature.
[40] Cesare Furlanello,et al. A promoter-level mammalian expression atlas , 2015 .
[41] Mark I. McCarthy,et al. Pancreatic islet enhancer clusters enriched in type 2 diabetes risk–associated variants , 2013, Nature Genetics.
[42] Manolis Kellis,et al. Systematic discovery and characterization of regulatory motifs in ENCODE TF binding experiments , 2013, Nucleic acids research.
[43] Joseph K. Pickrell. Joint analysis of functional genomic data and genome-wide association studies of 18 human traits , 2013, bioRxiv.
[44] C. Wallace,et al. Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics , 2013, PLoS genetics.
[45] Piero Carninci,et al. Detecting expressed genes using CAGE. , 2014, Methods in molecular biology.
[46] R. Young,et al. Super-Enhancers in the Control of Cell Identity and Disease , 2013, Cell.
[47] Stephen C. J. Parker,et al. Chromatin stretch enhancer states drive cell-specific gene regulation and harbor human disease risk variants , 2013, Proceedings of the National Academy of Sciences.
[48] Howard Y. Chang,et al. Transposition of native chromatin for fast and sensitive epigenomic profiling of open chromatin, DNA-binding proteins and nucleosome position , 2013, Nature Methods.
[49] Caleb Webber,et al. GAT: a simulation framework for testing the association of genomic intervals , 2013, Bioinform..
[50] Heng Li. Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM , 2013, 1303.3997.
[51] Łukasz M. Boryń,et al. Genome-Wide Quantitative Enhancer Activity Maps Identified by STARR-seq , 2013, Science.
[52] Juan M. Vaquerizas,et al. DNA-Binding Specificities of Human Transcription Factors , 2013, Cell.
[53] Buhm Han,et al. Chromatin marks identify critical cell types for fine mapping complex trait variants , 2012 .
[54] William Stafford Noble,et al. Integrative annotation of chromatin elements from ENCODE data , 2012, Nucleic acids research.
[55] Thomas R. Gingeras,et al. STAR: ultrafast universal RNA-seq aligner , 2013, Bioinform..
[56] Bronwen L. Aken,et al. GENCODE: The reference human genome annotation for The ENCODE Project , 2012, Genome research.
[57] Manolis Kellis,et al. Evidence of Abundant Purifying Selection in Humans for Recently Acquired Regulatory Functions , 2012, Science.
[58] Marc D. Perry,et al. ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia , 2012, Genome research.
[59] ENCODEConsortium,et al. An Integrated Encyclopedia of DNA Elements in the Human Genome , 2012, Nature.
[60] Manolis Kellis,et al. ChromHMM: automating chromatin-state discovery and characterization , 2012, Nature Methods.
[61] T. Mikkelsen,et al. Rapid dissection and model-based optimization of inducible enhancers in human cells using a massively parallel reporter assay , 2012, Nature Biotechnology.
[62] Michael F. Melgar,et al. Discovery of active enhancers through bidirectional expression of short transcripts , 2011, Genome Biology.
[63] Albert J. Vilella,et al. A high-resolution map of human evolutionary constraint using 29 mammals , 2011, Nature.
[64] Marcel Martin. Cutadapt removes adapter sequences from high-throughput sequencing reads , 2011 .
[65] William Stafford Noble,et al. FIMO: scanning for occurrences of a given motif , 2011, Bioinform..
[66] Timothy J. Durham,et al. Systematic analysis of chromatin state dynamics in nine human cell types , 2011, Nature.
[67] B. Bernstein,et al. Charting histone modifications and the functional organization of mammalian genomes , 2011, Nature Reviews Genetics.
[68] R. Young,et al. Histone H3K27ac separates active from poised enhancers and predicts developmental state , 2010, Proceedings of the National Academy of Sciences.
[69] Mazhar Adli,et al. Genome-wide chromatin maps derived from limited numbers of hematopoietic progenitors , 2010, Nature Methods.
[70] Manolis Kellis,et al. Discovery and characterization of chromatin states for systematic annotation of the human genome , 2010, Nature Biotechnology.
[71] G. Kreiman,et al. Widespread transcription at neuronal activity-regulated enhancers , 2010, Nature.
[72] Skipper Seabold,et al. Statsmodels: Econometric and Statistical Modeling with Python , 2010, SciPy.
[73] Gonçalo R. Abecasis,et al. The Sequence Alignment/Map format and SAMtools , 2009, Bioinform..
[74] Leighton J. Core,et al. Nascent RNA Sequencing Reveals Widespread Pausing and Divergent Initiation at Human Promoters , 2008, Science.
[75] A. Krogh,et al. A code for transcription initiation in mammalian genomes. , 2007, Genome research.
[76] T. Mikkelsen,et al. Genome-wide maps of chromatin state in pluripotent and lineage-committed cells , 2007, Nature.
[77] Inna Dubchak,et al. VISTA Enhancer Browser—a database of tissue-specific human enhancers , 2006, Nucleic Acids Res..
[78] Gerald P. Mckenny. Human Traits , 2007 .
[79] Alexander E. Kel,et al. TRANSFAC® and its module TRANSCompel®: transcriptional gene regulation in eukaryotes , 2005, Nucleic Acids Res..
[80] M. Ichihara,et al. GDNF-inducible zinc finger protein 1 is a sequence-specific transcriptional repressor that binds to the HOXA10 gene regulatory region , 2005, Nucleic acids research.
[81] B. Raaka,et al. Epithelial-to-Mesenchymal Transition Generates Proliferative Human Islet Precursor Cells , 2004, Science.
[82] A. Butte,et al. Coordinated reduction of genes of oxidative metabolism in humans with insulin resistance and diabetes: Potential role of PGC1 and NRF1 , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[83] Tom H. Pringle,et al. The human genome browser at UCSC. , 2002, Genome research.
[84] A. Sharrocks. The ETS-domain transcription factor family , 2001, Nature Reviews Molecular Cell Biology.
[85] Y. Benjamini,et al. THE CONTROL OF THE FALSE DISCOVERY RATE IN MULTIPLE TESTING UNDER DEPENDENCY , 2001 .
[86] 박귀태,et al. A Type 2 Diabetes–Associated Functional Regulatory Variant in a Pancreatic Islet Enhancer at the ADCY5 Locus , 2017, Diabetes.