同济大学嵌入式系统与服务计算教育部重点实验室

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“智信讲坛”(第八十一)期学术报告

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【保护视力背景色: 杏仁黄 秋叶褐 胭脂红 芥末绿 天蓝 雪青 灰 银河白(默认色)】 【字色: 绿 粉红 深蓝】 【字体:8 7 6 5 4 3 2 1


  题目:MSIQ: Joint Modeling of Multiple RNA-seq Samples for Accurate Isoform Quantification
  
  报告人:Jingyi Jessica Li
  
  时间: 2016年12月21日上午10:30-11:30am
  
  地点: 403会议室
  
  邀请人: 黄德双教授
  
  报告人简介:Dr. Jingyi Jessica Li is an Assistant Professor in the Department of Statistics and Department of Human Genetics at University of California, Los Angeles. She is also a faculty member in the Interdepartmental Ph.D. Program in Bioinformatics and a member in the Jonsson Comprehensive Cancer Center (JCCC) Gene Regulation Research Program Area. Prior to joining UCLA, she obtained her Ph.D. degree from the Interdepartmental Group in Biostatistics at University of California, Berkeley, where she worked with Profs Peter J. Bickel and Haiyan Huang. She received her B.S. (summa cum laude) from Department of Biological Sciences and Technology at Tsinghua University, China in 2007.
  
  内容提要:Next-generation RNA sequencing (RNA-seq) technology has been widely used to assess full-length RNA isoform abundance in a high-throughput manner. RNA-seq data offer insight into gene expression levels and transcriptome structure, enabling us to better understand the regulation of gene expression and fundamental biological processes. Accurate isoform quantification from RNA-seq data is a challenging task due to the information loss in sequencing experiments. Recent accumulation of multiple RNA-seq data sets from the same biological condition provides new opportunities to improve the isoform quantification accuracy. However, existing statistical or computational methods for multiple RNA-seq samples either pool the samples into one sample or assign equal weights to the samples in estimating isoform abundance. These methods ignore the possible heterogeneity in the quality of different samples, and could have biased and unrobust estimates.
  
  
  
  欢迎各位老师同学踊跃参加!
 
 

发布日期:2016-12-14

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