scholarly article | Q13442814 |
P2093 | author name string | Huntington F Willard | |
Zhong Wang | |||
P2860 | cites work | Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project | Q21061203 |
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Chromatin modifications and their function | Q27861067 | ||
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Histone acetylation and an epigenetic code | Q28143767 | ||
Cellular memory and the histone code | Q28213805 | ||
Transcription regulation by histone methylation: interplay between different covalent modifications of the core histone tails | Q28216534 | ||
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Topological domains in mammalian genomes identified by analysis of chromatin interactions | Q28264221 | ||
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Allele-specific chromatin immunoprecipitation studies show genetic influence on chromatin state in human genome | Q28469213 | ||
Chromosome bands, their chromatin flavors, and their functional features | Q28766216 | ||
A chromatin landmark and transcription initiation at most promoters in human cells | Q29547180 | ||
Mapping and analysis of chromatin state dynamics in nine human cell types | Q29547552 | ||
Genomic maps and comparative analysis of histone modifications in human and mouse | Q29614418 | ||
Evidence of influence of genomic DNA sequence on human X chromosome inactivation | Q33256101 | ||
The chromosomal high-affinity binding sites for the Drosophila dosage compensation complex. | Q33392676 | ||
ENCODE whole-genome data in the UCSC Genome Browser | Q33516102 | ||
Genome-wide analysis of histone modifications in human pancreatic islets | Q33762419 | ||
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Molecular control of pluripotency | Q36571557 | ||
GC- and AT-rich chromatin domains differ in conformation and histone modification status and are differentially modulated by Rpd3p | Q36672405 | ||
What is a support vector machine? | Q36679246 | ||
Global patterns of histone modifications | Q36743042 | ||
A sequence motif within chromatin entry sites directs MSL establishment on the Drosophila X chromosome | Q37034847 | ||
CpG islands influence chromatin structure via the CpG-binding protein Cfp1. | Q37061200 | ||
Local DNA topography correlates with functional noncoding regions of the human genome | Q37358871 | ||
What controls nucleosome positions? | Q37549548 | ||
Multiple spatially distinct types of facultative heterochromatin on the human inactive X chromosome | Q37694528 | ||
High-resolution, genome-wide mapping of chromatin modifications by GMAT. | Q38293369 | ||
Histone replacement marks the boundaries of cis-regulatory domains | Q38303903 | ||
Machine learning and its applications to biology | Q42734852 | ||
Human genome organization: Alu, LINES, and the molecular structure of metaphase chromosome bands | Q46063264 | ||
Dynamics of Replication-Independent Histone Turnover in Budding Yeast | Q57233862 | ||
SINEs and LINEs cluster in distinct DNA fragments of Giemsa band size | Q69565216 | ||
Nucleosome positions predicted through comparative genomics | Q80238247 | ||
P407 | language of work or name | English | Q1860 |
P921 | main subject | bias | Q742736 |
P304 | page(s) | 367 | |
P577 | publication date | 2012-08-02 | |
P1433 | published in | BMC Genomics | Q15765854 |
P1476 | title | Evidence for sequence biases associated with patterns of histone methylation | |
P478 | volume | 13 |
Q90066018 | Deciphering epigenomic code for cell differentiation using deep learning |
Q34330039 | Gene × environment interaction by a longitudinal epigenome-wide association study (LEWAS) overcomes limitations of genome-wide association study (GWAS) |
Q38835003 | Links between DNA methylation and nucleosome occupancy in the human genome |
Q30413241 | Retrotransposon Alu is enriched in the epichromatin of HL-60 cells |
Q36397888 | Stress and glucocorticoid receptor transcriptional programming in time and space: Implications for the brain-gut axis |
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