邵浩靖课题组

邵浩靖课题组 

Haojing Shao Lab

　　课题组长

       邵浩靖，副研究员，深圳市海外高层次人才。2018年博士毕业于澳大利亚昆士兰大学，研究方向为针对DNA测序数据数据的生物信息方法开发和分析，开发了npInv和SOAP-popIndel等算法软件。近年来使用自主研发的方法或现有方法对基因组变异进行研究，其结果作为成果的一部分发表到高水平学术期刊，获得引用共计6000余次并以第一作者在Nucleic Acids Research, Scientific Report, BMC Bioinformatics上发表学术论文3篇。

 

　　工作经历

　　2020.8–至今          爱彩人彩票     副研究员

　　2018.9–2020.6      昆士兰大学                                             博士后   

　　2009.3–2013.12    华大基因                                                课题组长

 

　　教育经历

　　2014.1–2018.8                昆士兰大学        博士 

　　2006.9–2010.6                华南理工大学    学士     

 

　　研究方向

       目前本课题组致力于空间转录组学研究。利用空间基因表达解决策略测量完整组织切片的总mRNA，将总mRNA的空间信息与形态学内容相结合，并绘制所有基因表达发生的位置，获得复杂而完整的基因表达图谱。利用不同基因、细胞群的空间位置探究基因及细胞功能、表型和组织微环境、发育等生物学问题,并构建3D转录组模型。此外，本课题组也致力于用信息分析的方法对基因组进行探索。目前大部分动物植物的基因组已经到达染色体水平，但是还没有到达100%完整的端粒到端粒水平。未知的序列主要是串联重复序列（着丝点或核糖体）或者是大片段重复序列。本课题组结合二代，三代，HiC等测序数据开发方法对这些基因组未知区域进行探索，并对其进行分析。

 

　　PI

      Haojing Shao, Associate Professor, Overseas High-Caliber Personnel. He graduated from The University of Queensland in 2018. His research interest is developing computational methods to analyze DNA sequencing data. He has developed computational methods called npInv and SOAP-popIndel. In recent years, he used his own methods or existing methods to study genomic variation, and the results have been published as part of his work in high-level academic journals, which have been quoted more than 6000 times in total.Besides,he also published three papers as the first author at Nucleic Acids Research, Scientific Report, BMC Bioinformatics.

　　

　　Research Experience

        2020-now      Shenzhen agricultural Genome Research Institute, Chinese Academy of Agricultural Sciences      Associate Professor

        2018-2020     The University of Queensland                                                                                                            Australia Postdoctoral Fellow

　　2009-2013     Shenzhen-Beijing Genomics Institute                                                                                                Leader of a Bioinformatics group

　　

　　Education 

　　2014-2018         The University of Queensland, Australia         Ph.D. of Bioinformatics, Supervised by Bernard Degnan and Sandie Degnan

　　2006-2010         South China University of Technology            Bachelor of Computer Science

 

　　Research Interest

       At present, our lab focuses on the study of spatial transcriptomics. We use spatial gene expression solution strategy to measure the total mRNA of the complete tissue sections, and we combine the spatial information of total mRNA with the morphological content to obtain the location of all gene expression and a complex and complete gene expression map. Then, we use the spatial location of different genes and cell populations to explore biological issues such as gene and cell functions, phenotype, tissue microenvironment and development, and constructed the 3D transcriptome model. In addition, our lab also aims to use computational methods to explore the genome. Currently, most animal and plant genomes are assembled at chromosome level, but they are not assembled at 100% complete telomere-to-telomere(T2T) level yet. The majority of the unknown sequences are tandem repeat sequences (centromere and ribosomal DNA array) and large segmental duplications. Our lab develops computational methods for next-generation sequencing, third-generation sequencing or Hi-C data to explore and analyze these unknown genetics regions.

　　

　　Selected Publication

　　1.  Shao, Haojing, et al. "npInv: accurate detection and genotyping of inversions mediated by non-allelic homologous recombination using long read sub-alignment." BMC bioinformatics 19 (1), 261 (2018).    (First Author)

　　2. Shao, Haojing, et al. "Ongoing human chromosome end extension driven by a primate ancestral genomic region revealed by analysis of BioNano genomics data." Scientific reports 8 (1), 16616 (2018)      (First Author)

　　3. Shao, Haojing, et al. "A population model for genotyping indels from next -generation sequence data." Nucleic acids research 41.3 (2012): e46-e46.    (First Author)

　　4. Li, Yingrui, et al. "Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly." Nature biotechnology 29.8 (2011): 723-730.  (co-author) 

　　5. Poznik, G. David, et al. "Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences." Nature genetics 48.6 (2016): 593-599.  (co-author)

　　6. 1000 Genomes Project Consortium. "A global reference for human genetic variation." Nature 526.7571 (2015): 68.   (co-author)

　　7. Tang, Huayang, et al. "A large-scale screen for coding variants predisposing to psoriasis." Nature genetics 46.1 (2014): 45. (co-author)

　　8. Zhou, Fusheng, et al. "Deep sequencing of the MHC region in the Chinese population contributes to studies of complex disease." Nature genetics 48.7 (2016): 740.   (co-author)

　　邵浩靖课题组更新于2021年7月