User:Kun Zhang: Difference between revisions

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<b>Kun Zhang, Ph.D.</b><br>
<b>Kun Zhang, Ph.D.</b><br>
Assistant Professor<br>
Associate Professor<br>
Department of Bioengineering<br>
Department of Bioengineering<br>
University of California, San Diego<br>
University of California, San Diego<br>
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[http://zhang.openwetware.org Zhang Lab Website]
[http://zhang.openwetware.org Zhang Lab Website]
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==Education==
 
*Post-doc, Department of Genetics, Harvard Medical School
*Ph.D., Human and Molecular Genetics, University of Texas-Houston/MD-Anderson Cancer Center
*M.S., Neuroscience, Fudan University, China
*B.S., Biophysics, Fudan University, China
==Research Interests==
==Research Interests==
We are developing genome technologies based on single-molecule sequencing, single-cell manipulation/amplification, and chip-based synthesis and manipulation of complex DNA libraries. We apply these novel technologies to stem cell genomics, personal genomes and human common diseases.
We are developing genome technologies related to single-cell analyses of genome, transcriptome and epigenome, as well as single-cell imaging and lineage tracing. We apply these novel technologies to stem cell fate conversion, human brain mapping and human disease studies.


==Publications==
==Publications==
#<b>Zhang K</b>, Li JB, Gao Y, Egli D, Xie B, Deng J, Li Z, Lee JH, Aach J, LeProust EM, Eggan K, Church GM (2009) Digital RNA allelotyping reveals tissue-specific and allele-specific gene expression in human. <b>Nature Methods</b>, 6:613-8
*[https://scholar.google.com/citations?user=CYeurYgAAAAJ&hl=en Google Scholar Page].
#Li JB, Gao Y, Aach J, <b>Zhang K</b>, Kryukov G, Xie B, Ahlford A, Yoon JK, Rosenbaum AM, Zaranek AW, ElProust E, Sunyaev S, Church GM. (2009) Multiplex padlock capture and sequencing reveal human hypermutable CpG variations. <b>Genome Research</b>, [http://genome.cshlp.org/content/early/2009/06/12/gr.092213.109.abstract Advanced Online Articles]
#Li JB, Levanon EY, Yoon J-K, Aach J, Xie B, LeProust E, <b>Zhang K</b>, Gao Y, Church GM (2009) Genome-wide Identification of Human RNA Editing Sites by Massively Parallel DNA Capturing and Sequencing, <b>Science</b> 324:1210-13
#Deng J, Shoemaker R, Xie B, Gore A, Leproust EM, Antosiewicz-Bourget J, Egli D, Maherali N, Park IH, Yu J, Daley GQ, Eggan K, Hochedlinger K, Thomson J, Wang W, Gao Y, <b>Zhang K</b>. (2009) Targeted bisulfite sequencing reveals changes in DNA methylation associated with nuclear reprogramming. <b>Nature Biotechnology</b>, 27:353-60 [http://genome-tech.ucsd.edu/public/NBT-RA20324/Deng-NBT-2009.pdf PDF]
#Chen AE, Egli D, Niakan K, Deng J, Akutsu H, Yamaki M, Cowan C, Fitz-Gerald C, <b>Zhang K</b>, Melton DA, and Eggan K. (2009) Optimal timing of inner cell mass isolation increases the efficiency of human embryonic stem cell derivation and allows generation of sibling cell lines. <b>Cell Stem Cell</b> 4:103-6
#Porreca PJ, <b>Zhang K (co-first author)</b>, Li JB, Xie B, Austin D, Vassallo SL, Leproust EM, Peck BJ, Emig CJ, Dahl F, Gao Y, Church GM, Shendure J. (2007) Multiplex amplification of large sets of human exons. <b>Nature Methods</b> 4:931-6.
#Kowalchuk GA, Speksnijder AG, <b>Zhang K</b>, Goodman RM, van Veen JA. (2007) Finding the needles in the metagenome haystack. <b>Microbial Ecology</b> 53:475-85
#<b>Zhang K</b>, Lott ST, Jin L, Killary AM. (2007) Fine mapping of the NRC-1 tumor suppressor locus within chromosome 3p12. <b>Biochemical and Biophysical Research Communications</b> 360:531-538
#<b>Zhang K</b>, Martiny AC, Reppas NB, Barry KW, Malek J, Chisholm SW, Church GM. (2006) Sequencing genomes from single cells by polymerase cloning. <b>Nature Biotechnology</b> 24:680-686
#<b>Zhang K</b>, Zhu J, Shendure J, Porreca GJ, Aach JD, Mitra RD, Church GM. (2006) Polony haplotyping of individual human chromosome molecules. <b>Nature Genetics</b> 38:382-387.
#Shendure J, Porreca GJ, Reppas NB, Lin X, McCutcheon JP, Rosenbaum AM, Wang MD, <b>Zhang K</b>, Mitra RD, Church GM. (2005) Accurate multiplex polony sequencing of an evolved bacterial genome. <b>Science</b> 309:1728-1732.
#<b>Zhang K</b>, and Jin L. (2003) HaploBlockFinder: haplotype block analyses. <b>Bioinformatics</b> 19:1300-1301
#<b>Zhang K</b>, Akey JM (co-first author), Wang N, Xiong M, Chakraborty R, Jin L.(2003) Randomly distributed crossovers may generate block-like pattern of linkage disequibrium: An act of genetic drift. <b>Human Genetics</b> 113: 51-59.
#Akey JM, <b>Zhang K</b>, Xiong M, and Jin L. (2003) The effect of single nucleotide polymorphism identification strategies on estimates of linkage disequilibrium. <b>Molecular Biology and  Evolution</b> 20: 232-242. 
#Chen Z, <b>Zhang K</b>, Zhang X, Yuan XH, Yuan Z, Jin L, and Xiong M. (2003) Comparison of gene expression between metastatic derivatives and their poorly metastatic parental cells implicates crucial tumor-environment interaction in metastasis of head and neck squamous cell carcinoma. <b>Clinical and Experimental Metastasis</b> 20:335-342.
#Akey JM, Zhang G, Z<b>hang K</b>, Jin L and Shriver M. (2002) Interrogating a high-density SNP map for signatures of natural selection. <b>Genome Research</b> 12: 1805-1814.
#Wang N, Akey JM, <b>Zhang K</b>, Chakraborty R, Jin L. (2002)  Distribution of recombination crossovers and the origin of haplotype blocks: the interplay of population history, recombination, and mutation. <b>American Journal of Human Genetics</b> 71: 1227-1234.
#Akey DT, Akey JM, <b>Zhang K</b>, Jin L. (2002) Assaying DNA methylation based on high-throughput melting curve approaches. <b>Genomics</b> 80: 376-384.
#Akey JM, <b>Zhang K (co-first author)</b>, Xiong M, Doris P, Jin L. (2001) The effect that genotyping errors have on the robustness of common linkage-disequilibrium measures. <b>American Journal of Human Genetics</b>, 68:1447-1456.

Revision as of 12:48, 9 February 2015

Kun Zhang, Ph.D.
Associate Professor
Department of Bioengineering
University of California, San Diego
9500 Gilman Drive, MC0412
La Jolla, CA 92903
Zhang Lab Website

Research Interests

We are developing genome technologies related to single-cell analyses of genome, transcriptome and epigenome, as well as single-cell imaging and lineage tracing. We apply these novel technologies to stem cell fate conversion, human brain mapping and human disease studies.

Publications