DiseaseEnhancer: a resource of human disease-associated enhancer catalog
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics
Link
http://academic.oup.com/nar/article-pdf/46/D1/D78/23162729/gkx920.pdf
Reference36 articles.
1. Systematic localization of common disease-associated variation in regulatory DNA;Science,2012
2. Genetic and epigenetic fine mapping of causal autoimmune disease variants;Nature,2015
3. Evaluation of the RET regulatory landscape reveals the biological relevance of a HSCR-implicated enhancer;Hum. Mol. Genet.,2005
4. Recurrent somatic mutations in regulatory regions of human cancer genomes;Nat. Genet.,2015
5. The non-coding variant rs1800734 enhances DCLK3 expression through long-range interaction and promotes colorectal cancer progression;Nat. Commun.,2017
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2. NCAD v1.0: A database for non-coding variant annotation and interpretation;Journal of Genetics and Genomics;2023-12
3. Integrative approaches based on genomic techniques in the functional studies on enhancers;Briefings in Bioinformatics;2023-11-22
4. iEnhancer-DCSA: identifying enhancers via dual-scale convolution and spatial attention;BMC Genomics;2023-07-13
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