Hui Jiang

Summary

Affiliation: Chinese Academy of Sciences
Country: China

Publications

  1. pmc PSCC: sensitive and reliable population-scale copy number variation detection method based on low coverage sequencing
    Xuchao Li
    BGI Shenzhen, Shenzhen, China
    PLoS ONE 9:e85096. 2014
  2. pmc Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies
    Fuman Jiang
    BGI Shenzhen, Shenzhen, China
    BMC Med Genomics 5:57. 2012
  3. pmc Comprehensive comparison of three commercial human whole-exome capture platforms
    - Asan
    Beijing Institute of Genomics, Chinese Academy of Sciences, No 7 Beitucheng West Road, Chaoyang District, Beijing 100029, China
    Genome Biol 12:R95. 2011
  4. pmc Comprehensive evaluation of SNP identification with the Restriction Enzyme-based Reduced Representation Library (RRL) method
    Ye Du
    BGI_shenzhen, Shenzhen 518000, China
    BMC Genomics 13:77. 2012
  5. pmc High resolution profiling of human exon methylation by liquid hybridization capture-based bisulfite sequencing
    Junwen Wang
    Beijing Genomics Institute at Shenzhen, Beishan Road, Shenzhen 518000, China
    BMC Genomics 12:597. 2011
  6. pmc Noninvasive prenatal detection for pathogenic CNVs: the application in α-thalassemia
    Huijuan Ge
    Fetal Medicine Center, Department of Obstetrics and Gynecology, First Affiliated Hospital of Sun Yat sen University, Guangzhou, Guangdong Province, China BGI Shenzhen, Shenzhen, China
    PLoS ONE 8:e67464. 2013
  7. doi Massively parallel sequencing for chromosomal abnormality testing in trophectoderm cells of human blastocysts
    Xuyang Yin
    BGI Shenzhen, Shenzhen, China
    Biol Reprod 88:69. 2013
  8. doi Rapid detection of aneuploidies on a benchtop sequencing platform
    Weiwei Xie
    BGI Shenzhen, Shenzhen, China
    Prenat Diagn 33:232-7. 2013
  9. pmc Effective noninvasive zygosity determination by maternal plasma target region sequencing
    Jing Zheng
    Science and Technology, BGI Shenzhen, Shenzhen, China
    PLoS ONE 8:e65050. 2013
  10. doi A method for noninvasive detection of fetal large deletions/duplications by low coverage massively parallel sequencing
    Shengpei Chen
    BGI Shenzhen, Shenzhen, China
    Prenat Diagn 33:584-90. 2013

Collaborators

  • Fang Chen
  • Wei Wang
  • Fuman Jiang
  • Jun Wang
  • Bo Xiong
  • Ida Vogel
  • Qun Fang
  • Chang Yu
  • Nikki P Lee
  • Lei Zhang
  • Jian Xu
  • Gabor Vajta
  • Ping Liu
  • Shengpei Chen
  • Xuchao Li
  • Chunlei Zhang
  • Xiuqing Zhang
  • Weiwei Xie
  • Xiaoyu Pan
  • Huijuan Ge
  • Jing Zheng
  • Xun Xu
  • Xuyang Yin
  • Ge Lin
  • Yingrui Li
  • Yueqiu Tan
  • Guangxiu Lu
  • Weiyang Li
  • Chunsheng Zhang
  • Jing Guo
  • Hefeng Huang
  • Ling Pan
  • Chenming Xu
  • Ping Hu
  • Zhengfeng Xu
  • Songgang Li
  • Ke Tan
  • Xiao Liu
  • Ye Du
  • - Asan
  • Hancheng Zheng
  • Sheng Li
  • Yongqiang Deng
  • Fang Huang
  • Jia Sophie Liu
  • Kwong Wai Choy
  • Rikke Christensen
  • Tze Kin Lau
  • Guan Wang
  • Hongyun Zhang
  • Fei Gong
  • Xuehan Zhuang
  • - Jianwang
  • Ronnie T Poon
  • Chun Gong
  • Xuan Huang
  • Feng Mu
  • Shuoping Zhang
  • Huanhuan Peng
  • Ya Gao
  • Sheung Tat Fan
  • Bing Guo
  • Lijian Zhao
  • Chuyu Lin
  • Yu Liang
  • Xin Yi
  • Xi Zeng
  • Ning Chen
  • Yuan Wei
  • Shang Yi
  • Mao Mao
  • Yangyu Zhao
  • Weiping Tang
  • Dehua Cheng
  • Cong Li
  • Ying Chen
  • Meiru Zhao
  • Qibin Li
  • Jinghua Wu
  • Yong Qiu
  • Yu Xu
  • Mingzhi Wu
  • Chris Tyler-Smith
  • Geng Tian
  • Yali Xue
  • Tao Jiang
  • Huangming Yang

Detail Information

Publications13

  1. pmc PSCC: sensitive and reliable population-scale copy number variation detection method based on low coverage sequencing
    Xuchao Li
    BGI Shenzhen, Shenzhen, China
    PLoS ONE 9:e85096. 2014
    ..In this study, using low coverage whole-genome sequencing (LCS) we have developed an effective population-scale CNV calling (PSCC) method...
  2. pmc Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies
    Fuman Jiang
    BGI Shenzhen, Shenzhen, China
    BMC Med Genomics 5:57. 2012
    ..Conventional prenatal screening tests, such as maternal serum tests and ultrasound scan, have limited resolution and accuracy...
  3. pmc Comprehensive comparison of three commercial human whole-exome capture platforms
    - Asan
    Beijing Institute of Genomics, Chinese Academy of Sciences, No 7 Beitucheng West Road, Chaoyang District, Beijing 100029, China
    Genome Biol 12:R95. 2011
    ..Currently, there are several commercial human exome capture platforms; however, the relative performances of these have not been characterized sufficiently to know which is best for a particular study...
  4. pmc Comprehensive evaluation of SNP identification with the Restriction Enzyme-based Reduced Representation Library (RRL) method
    Ye Du
    BGI_shenzhen, Shenzhen 518000, China
    BMC Genomics 13:77. 2012
    ..It has remarkable advantage of reducing the complexity of the genome by orders of magnitude. However, comprehensive evaluation for actual efficacy of SNP identification by this method is still unavailable...
  5. pmc High resolution profiling of human exon methylation by liquid hybridization capture-based bisulfite sequencing
    Junwen Wang
    Beijing Genomics Institute at Shenzhen, Beishan Road, Shenzhen 518000, China
    BMC Genomics 12:597. 2011
    ..Thus, they are not practical for researchers to study multiple clinical samples in biomarker research...
  6. pmc Noninvasive prenatal detection for pathogenic CNVs: the application in α-thalassemia
    Huijuan Ge
    Fetal Medicine Center, Department of Obstetrics and Gynecology, First Affiliated Hospital of Sun Yat sen University, Guangzhou, Guangdong Province, China BGI Shenzhen, Shenzhen, China
    PLoS ONE 8:e67464. 2013
    ..However, few studies discussed the possibility of noninvasive pathogenic CNVs detection...
  7. doi Massively parallel sequencing for chromosomal abnormality testing in trophectoderm cells of human blastocysts
    Xuyang Yin
    BGI Shenzhen, Shenzhen, China
    Biol Reprod 88:69. 2013
    ..Our study demonstrated MPS could be applied to accurately detect embryonic chromosomal abnormality with a flexible and cost-effective strategy and higher potential accuracy...
  8. doi Rapid detection of aneuploidies on a benchtop sequencing platform
    Weiwei Xie
    BGI Shenzhen, Shenzhen, China
    Prenat Diagn 33:232-7. 2013
    ..To report a novel method of rapidly detecting fetal aneuploidies for spontaneous abortion using ultra-low whole genome sequencing data on a benchtop sequencing platform...
  9. pmc Effective noninvasive zygosity determination by maternal plasma target region sequencing
    Jing Zheng
    Science and Technology, BGI Shenzhen, Shenzhen, China
    PLoS ONE 8:e65050. 2013
    ..This study aimed to develop a novel method to determine zygosity by using maternal plasma target region sequencing...
  10. doi A method for noninvasive detection of fetal large deletions/duplications by low coverage massively parallel sequencing
    Shengpei Chen
    BGI Shenzhen, Shenzhen, China
    Prenat Diagn 33:584-90. 2013
    ..To report the feasibility of fetal chromosomal deletion/duplication detection using a novel bioinformatic method of low coverage whole genome sequencing of maternal plasma...
  11. pmc Performance comparison between rapid sequencing platforms for ultra-low coverage sequencing strategy
    Shengpei Chen
    State Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering, Southeast University, Nanjing, China BGI Shenzhen, Shenzhen, China Shenzhen Municipal Key Laboratory of Birth Defects Screening and Engineering, BGI Shenzhen, Shenzhen, China Guangdong Provincial Key Laboratory of Human Diseases Genome, BGI Shenzhen, Guangdong, China BGI Nanjing, Nanjing, China The Key Technology R and D Program of Jiangsu Province, Nanjing, China
    PLoS ONE 9:e92192. 2014
    ..Our study generated essential data from these two rapid sequencing platforms, which provides useful reference for later research and potentially accelerates the clinical applications of ULCS. ..
  12. doi HIVID: an efficient method to detect HBV integration using low coverage sequencing
    Weiyang Li
    BGI Shenzhen, Shenzhen, 518083, China School of Bioscience and Bioengineering, South China University of Technology, China
    Genomics 102:338-44. 2013
    ..7% (10/15) of validation rate. Our study shows HIVID is a cost-effective methodology with high specificity and sensitivity to identify viral integration in human genome. ..
  13. pmc A single cell level based method for copy number variation analysis by low coverage massively parallel sequencing
    Chunlei Zhang
    Science and Technology, BGI Shenzhen, Shenzhen, China
    PLoS ONE 8:e54236. 2013
    ....