Hancheng Zheng

发表

A Reference Feature based method for Quantification and Identification of LC-MS based untargeted metabolomics

Dehua Li, Lei Feng, Wei Li, 2020, bioRxiv.

Whole-genome sequencing identifies recurrent mutations in hepatocellular carcinoma

Lin Li, Shibing Deng, Hongyue Dai, 2013, Genome research.

Whole-Genome Sequencing in Autism Identifies Hot Spots for De Novo Germline Mutation

Lilia M. Iakoucheva, Jun Wang, Dheeraj Malhotra, 2012, Cell.

Building the sequence map of the human pan-genome

Lars Bolund, Ruiqiang Li, Xuan Zhu, 2010, Nature Biotechnology.

Discovery of biclonal origin and a novel oncogene SLC12A5 in colon cancer by single-cell sequencing

Jian Wang, Renhua Wu, Xun Xu, 2014, Cell Research.

MacArthur Protein-Coding Genes A Systematic Survey of Loss-of-Function Variants in Human

Klaudia Walter, Joseph K. Pickrell, Jennifer Harrow, 2012 .

Haplotype-assisted accurate non-invasive fetal whole genome recovery through maternal plasma sequencing

Jian Wang, Wei Wang, Hui Jiang, 2013, Genome Medicine.

De novo assembly of a haplotype-resolved human genome

Jian Wang, Xun Xu, Lars Bolund, 2015, Nature Biotechnology.

Consortium, G.P A map of human genome variation from population-scale sequencing. Nature 467, 1061-1073

Ken Chen, Joshua M. Korn, Afidalina Tumian, 2010 .

Whole-genome sequencing of matched primary and metastatic hepatocellular carcinomas

Yujian Shi, Hancheng Zheng, Zhuolin Gong, 2014, BMC Medical Genomics.