| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1026500560 |
| P356 | DOI | 10.1186/S13059-015-0621-5 |
| P2888 | exact match | https://scigraph.springernature.com/pub.10.1186/s13059-015-0621-5 |
| P932 | PMC publication ID | 4407537 |
| P698 | PubMed publication ID | 25887522 |
| P5875 | ResearchGate publication ID | 275102417 |
| P50 | author | Thomas Juettemann | Q55163283 |
| Daniel R Zerbino | Q37392174 | ||
| Nathan Johnson | Q55155214 | ||
| Paul Flicek | Q28359506 | ||
| Steven P Wilder | Q30503485 | ||
| P2860 | cites work | Ensembl variation resources | Q21030509 |
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| Human DNA methylomes at base resolution show widespread epigenomic differences | Q24633677 | ||
| Principles for the post-GWAS functional characterization of cancer risk loci | Q35887461 | ||
| Unsupervised pattern discovery in human chromatin structure through genomic segmentation | Q35923331 | ||
| The key to development: interpreting the histone code? | Q36083253 | ||
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| DNase-seq: a high-resolution technique for mapping active gene regulatory elements across the genome from mammalian cells | Q24633746 | ||
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| FAIRE (Formaldehyde-Assisted Isolation of Regulatory Elements) isolates active regulatory elements from human chromatin | Q24673476 | ||
| The landscape of histone modifications across 1% of the human genome in five human cell lines | Q24673723 | ||
| VISTA Enhancer Browser--a database of tissue-specific human enhancers | Q24676452 | ||
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| The UCSC genome browser and associated tools | Q28273417 | ||
| Ensembl 2013 | Q28280494 | ||
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| Nuclear organization of the genome and the potential for gene regulation | Q28303751 | ||
| An oestrogen-receptor-α-bound human chromatin interactome | Q29541719 | ||
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| BEDTools: a flexible suite of utilities for comparing genomic features | Q29547332 | ||
| Mapping and analysis of chromatin state dynamics in nine human cell types | Q29547552 | ||
| A genome-wide association study of global gene expression | Q29614592 | ||
| The Ensembl automatic gene annotation system | Q29614683 | ||
| Heterochromatin revisited | Q29614716 | ||
| Relative impact of nucleotide and copy number variation on gene expression phenotypes | Q29614883 | ||
| Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome | Q29616819 | ||
| Transcription regulation and animal diversity | Q29618752 | ||
| A signal-noise model for significance analysis of ChIP-seq with negative control | Q33550016 | ||
| eHive: an artificial intelligence workflow system for genomic analysis | Q33575547 | ||
| Transposition of native chromatin for fast and sensitive epigenomic profiling of open chromatin, DNA-binding proteins and nucleosome position | Q34375601 | ||
| A promoter-level mammalian expression atlas | Q34412203 | ||
| Cancer as an epigenetic disease: DNA methylation and chromatin alterations in human tumours | Q34465751 | ||
| Evidence for an instructive mechanism of de novo methylation in cancer cells. | Q34489258 | ||
| Integrative annotation of chromatin elements from ENCODE data | Q34503932 | ||
| Mapping networks of physical interactions between genomic elements using 5C technology | Q34578862 | ||
| An atlas of active enhancers across human cell types and tissues | Q34660689 | ||
| WiggleTools: parallel processing of large collections of genome-wide datasets for visualization and statistical analysis | Q35074245 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P304 | page(s) | 56 | |
| P577 | publication date | 2015-03-24 | |
| P1433 | published in | Genome Biology | Q5533480 |
| P1476 | title | The ensembl regulatory build | |
| P478 | volume | 16 |
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| Q28603093 | Ensembl 2016 |
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| Q64092405 | Genetic regulation of methylation in human endometrium and blood and gene targets for reproductive diseases |
| Q38621387 | Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations. |
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| Q91683266 | HACER: an atlas of human active enhancers to interpret regulatory variants |
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