C
Cheng Li
Researcher at Peking University
Publications - 238
Citations - 49764
Cheng Li is an academic researcher from Peking University. The author has contributed to research in topics: Gene & Medicine. The author has an hindex of 63, co-authored 200 publications receiving 42539 citations. Previous affiliations of Cheng Li include University of California, Los Angeles & Tongji University.
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ChipInfo: software for extracting gene annotation and gene ontology information for microarray analysis
TL;DR: ChipInfo is designed for retrieving annotation information from online databases and organizing such information into easily interpretable tabular format outputs and enables users to independently update the information resource files of these software packages.
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Clonal evolution and devolution after chemotherapy in adult acute myelogenous leukemia
Brian Parkin,Peter Ouillette,Yifeng Li,Jennifer A. Keller,Cindy Lam,Diane Roulston,Cheng Li,Kerby Shedden,Sami N. Malek +8 more
TL;DR: In this article, the authors used SNP 6.0 array-based genomic profiling of acquired copy number aberrations (aCNA) and copy neutral LOH (cnLOH) together with sequence analysis of recurrently mutated genes to characterize paired AML genomes.
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SET1A-Mediated Mono-Methylation at K342 Regulates YAP Activation by Blocking Its Nuclear Export and Promotes Tumorigenesis.
Lan Fang,Hongqi Teng,Yilin Wang,Guanghong Liao,Linjun Weng,Yaxu Li,Xinbo Wang,Jiali Jin,Chenchen Jiao,Lei Chen,Xiaoping Peng,Jiayu Chen,Yongzhi Yang,Houqin Fang,Dongyan Han,Cheng Li,Xueling Jin,Shihao Zhang,Zhongchen Liu,Min Liu,Qing Wei,Lujian Liao,Xin Ge,Bin Zhao,Dawang Zhou,Huanlong Qin,Jun Zhou,Ping Wang +27 more
TL;DR: It is demonstrated that YAP is a nucleocytoplasmic shuttling protein and its nuclear export is controlled by SET1A-mediated mono-methylation of YAP at K342, which disrupts the binding of Y AP to CRM1.
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Profiling chromatin states using single-cell itChIP-seq.
Shanshan Ai,Haiqing Xiong,Chen Li,Yingjie Luo,Qiang Shi,Yaxi Liu,Xianhong Yu,Cheng Li,Aibin He +8 more
TL;DR: Using sc-itChIP-seq to profile H3K27ac, the earliest epigenetic priming event during the cell fate transition from naive to primed pluripotency is captured, and the basis for cell-type specific enhancer usage during the differentiation of bipotent cardiac progenitor cells into endothelial cells and cardiomyocytes is revealed.
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SNP array analysis in hematologic malignancies: avoiding false discoveries
TL;DR: Examples from patients with myeloid malignancies are used to demonstrate the superiority of matched tumor and normal DNA samples over multiple unpaired samples with respect to reducing false discovery rates in high-resolution single nucleotide polymorphism array analysis.