2014第四届《自然遗传》疾病基因组学国际研讨会_门票优惠

While GWAS and epigenomics have gone a long way to map the regulatory variation in the human genome that is relevant to medical traits and epidemiological risk of disorders, sequencing based strategies are increasingly employed to dig ever deeper into the full spectrum of common, low frequency and rare variation that contributes to health and disease. At the same time, international consortia are making inroads into the constitutional and somatic variation that drives a range of cancers. This meeting provides a forum to connect these promising discoveries with the very practical need to develop from genomics a causal understanding of pathogenesis and mechanisms of diseases. At the same time, we expect to find therapeutic targets and biomarkers for improving clinical practice and public health. This is the meeting in which to coordinate this field and to have these discussions.

This conference, co-organized by Nature Genetics, Chinese Academy of Medical Sciences and Anhui Medical University in China and, will discuss the new progress in the genetic and genomic analysis of diseases and explore the challenges and roadblocks for moving beyond into medical biology. The following topics will be covered in the conference:

Common variants in disease
Analysis of low frequency variants
Translational genomics
Workshop: Somatic variants in cance

Thursday, May 15
8:00 – 1:00 pm	Registration（Radegast Lake View Hotel）
2:00 – 2:10 pm	Opening ceremony: Chaired by Xuetao Cao, Chinese Academy of Medical Science, China Opening remark: Xuejun Zhang, Anhui Medical University, China Myles Axton, Nature Genetics, USA
2:10 – 2:30 pm	Special lecture: Zhu Chen, Shanghai Jiao Tong University, China, Chaired by Xuetao Cao, Chinese Academy of Medical Science, China
Keynote lecture
Chair	Dongxin Lin, Chinese Academy of Medical Science ,China
2:30 – 3:30 pm	Andrew Hattersley (Exeter U., UK) Title: TBD
Session 1: Common variants
Chair	Yusuke Nakamura, University of Chicago, Chicago, IL, USA Xue Zhang, Chinese Academy of Medical Science, China
3:30 – 4:00 pm	M. R. Nelson，Quantitative Sciences, GlaxoSmithKline，USA Title: Human genetic evidence supports approved drug indications
4:00 – 4:20 pm	Coffee break
4:20 – 4:50 pm	Nicholas Schork, J. Craig Venter Institute，USA Title: Accommodating Heterogeneity in Association Analysis
4:50 – 5:20 pm	Xianbo Zuo, Anhui Medical University, China Title: Whole exome analysis reveals 21 coding variants for psoriasis
5:20 – 6:20 pm	1hr Roundtable Discussion
7:00 pm	Conference Dinner
Friday, May 16
Keynote lecture
Chair	Jing Cheng, Tsinghua University, China
8:30 – 9:30 am	Qimin Zhan , Chinese Academy of Medical Sciences，China Title: TBD
Session 2: Analysis of low frequency variants
Chair	Andrew Hattersley (University of Exeter, UK) Zhanguo Li, Peking Universtiy ,China
9:30 – 10:00 am	Jeong-Sun Seo, Seoul National University, Korea Title: Mutation profile and transriptomic analysis in lung adenocarcinoma, integrated with DNA methylation
10:00 – 10:30 am	Bruno Reversade, Institute of Medical Biology, A*STAR, Singapore Title: A Tale of Two Heritable Self-healing Skin Cancers
10:30 – 10:50 am	Coffee Break
10:50 – 11:20 am	Qinghua Shi, University of Science and Technology of China, China Title: Exome sequencing identifies mutations in Sertoli Cell Only Syndrome
11:20 – 12:20 pm	1hr Roundtable discussion
12:20 – 1:20 pm	Lunch seminar: 1. Future of Companion Diagnostics for Precision Oncology Frank S. Ong, MD，Associate Director, Medical Affairs Illumina IVD Development 2. Holistic Approaches to Complex Disease Studies using Arrays and Sequencing Technology from Illumina Carsten Rosenow, Associate Director, Global Sales illumina
Keynote lecture
Chair	Hongbing Shen, Nanjing Medical University, China
2:00 – 3:00 pm	Yusuke Nakamura, University of Chicago, USA Title: Cancer Genomics and Immunogenomics in Precision Medicine
Session 3: Translational genomics
Chair	Jianjun Liu, Anhui Medical University, China Joshua Stuart , University of California Santa Cruz, USA
3:00 – 3:30 pm	YT Chen, Institute of Biomedical Sciences, Academia Sinica, Taiwan Title: Translating Pharmacogenomics Findings into Clinic: Preventing Severe Drug Hypersensitivity with a Gene Test
3:30 – 3:50 pm	Coffee break
3:50 – 4:10 pm	Liang Wang, Medical College of Wisconsin, USA Title: Uncover the missing links between GWAS findings and underlying biology
4:10 – 4:40 pm	Jie Wang, Peking University, China Title: Heterogeneous SNVs/INDELs and Reproducible Copy Number Variation Patterns among Single Circulating Tumor Cells of Lung Cancer Patients
4:40 – 5:10 pm	BGI Title: TBD
5:10 – 6:10 pm	1hr Roundtable discussion
7:00 pm	Conference Dinner
Saturday, May 17
Keynote lecture
Chair	Myles Axton, Nature Genetics, USA
8:00 – 9:00 am	Joshua M Stuart, University of California Santa Cruz, USA Title: Pan-cancere to personalized cellular wiring diagrams of tumor cells
Education Session: Somatic variants in cancer
Chair	Myles Axton, Nature Genetics, USA
9:00 – 9:30 am	Jinghui Zhang, St Jude Children's Research Hospital, USA Title: Decoding Pediatric Cancer Genome by Whole Genome Sequencing
9:30 – 10:00 am	TBD
10:00 –10:20 am	Coffee Break
10:20 – 10:50 am	Ren Shan Cheng, Second Military Medical University, China Title: Genetic complexity in prostate cancer Revealed by whole genome and transcriptome sequencing
10:50 – 11:50 pm	1hr Roundtable discussion
11:50 – 12:30 pm	Myles Axton Nature Genetics, USA Title: TBD
12:30 – 1:40 pm	Conference Lunch

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会议标签：

医学年会

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