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Xinchen Wang

Researcher at Massachusetts Institute of Technology

Publications -  35
Citations -  14165

Xinchen Wang is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: Alternative splicing & Medicine. The author has an hindex of 20, co-authored 30 publications receiving 11871 citations. Previous affiliations of Xinchen Wang include Broad Institute & University of Toronto.

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Integrative analysis of 111 reference human epigenomes

Anshul Kundaje, +123 more
- 19 Feb 2015 - 
TL;DR: It is shown that disease- and trait-associated genetic variants are enriched in tissue-specific epigenomic marks, revealing biologically relevant cell types for diverse human traits, and providing a resource for interpreting the molecular basis of human disease.

Integrative analysis of 111 reference human epigenomes

TL;DR: In this article, the authors describe the integrative analysis of 111 reference human epigenomes generated as part of the NIH Roadmap Epigenomics Consortium, profiled for histone modification patterns, DNA accessibility, DNA methylation and RNA expression.
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Transcriptomic analysis of autistic brain reveals convergent molecular pathology

TL;DR: The results provide strong evidence for convergent molecular abnormalities in ASD, and implicate transcriptional and splicing dysregulation as underlying mechanisms of neuronal dysfunction in this disorder.
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Deciphering the splicing code

TL;DR: The assembly of a ‘splicing code’ is described, which uses combinations of hundreds of RNA features to predict tissue-dependent changes in alternative splicing for thousands of exons and facilitates the discovery and detailed characterization of regulatedAlternative splicing events on a genome-wide scale.
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Tissue-Specific Alternative Splicing Remodels Protein-Protein Interaction Networks

TL;DR: In this paper, the authors observed that brain and other tissue-regulated exons are significantly enriched in flexible regions of proteins that likely form conserved interaction surfaces, including Bridging Integrator 1 (Bin1)/Amphiphysin II and Dynamin 2 (Dnm2).