• DocumentCode
    2039352
  • Title

    Cell type specific analysis of human transcriptome data

  • Author

    Xiaoxiao Xu ; Nehorai, Arye ; Dougherty, John

  • Author_Institution
    Preston M. Green Dept. of Electr. & Syst. Eng., Washington Univ. in St. Louis, St. Louis, MO, USA
  • fYear
    2012
  • fDate
    2-4 Dec. 2012
  • Firstpage
    99
  • Lastpage
    100
  • Abstract
    The central nervous system (CNS) is composed of hundreds of distinct cell types, each expressing different subsets of genes from the genome. High throughput gene expression analysis of complex tissues like the CNS from patients and controls is a common method to screen for potentially pathological molecular mechanisms of psychiatric disease. One mechanism by which gene expression might be seen to vary across samples would be alterations in the cellular composition of the tissue. While there are a few gene `markers´ from literature for each cell type, their expression patterns vary significantly resulting in poor sensitivity and specificity. Here, we propose a method utilizing prior information from cell specific transcriptome profiling experiments in mice and co-expression network analysis to select cell type specific gene markers, and further to analytically detect changing cellular composition in human tissues. Our method successfully detects changes in cellularity over time that roughly correspond to known epochs of human brain development.
  • Keywords
    biological tissues; brain; cellular biophysics; diseases; genetics; genomics; neurophysiology; cell specific transcriptome profiling experiments; cell type specific analysis; cell type specific gene markers; cellular composition; central nervous system; coexpression network analysis; complex tissues; expression patterns; gene subsets; genome; high throughput gene expression analysis; human brain epochs; human tissues; human transcriptome data; mice; pathological molecular mechanisms; psychiatric disease;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Genomic Signal Processing and Statistics, (GENSIPS), 2012 IEEE International Workshop on
  • Conference_Location
    Washington, DC
  • ISSN
    2150-3001
  • Print_ISBN
    978-1-4673-5234-5
  • Type

    conf

  • DOI
    10.1109/GENSIPS.2012.6507737
  • Filename
    6507737