Warning: Undefined variable $zfal in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 525
Deprecated: str_replace(): Passing null to parameter #3 ($subject) of type array|string is deprecated in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 525

Warning: Undefined variable $sterm in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 530
free
Warning: Undefined variable $sterm in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 531
free
free
  English Wikipedia
Nephropedia Template TP (
Twit Text
DeepDyve Pubget Overpricing |   
lüll MiDReG: a method of mining developmentally regulated genes using Boolean implications Sahoo D; Seita J; Bhattacharya D; Inlay MA; Weissman IL; Plevritis SK; Dill DLProc Natl Acad Sci U S A 2010[Mar]; 107 (13): 5732-7We present a method termed mining developmentally regulated genes (MiDReG) to predict genes whose expression is either activated or repressed as precursor cells differentiate. MiDReG does not require gene expression data from intermediate stages of development. MiDReG is based on the gene expression patterns between the initial and terminal stages of the differentiation pathway, coupled with "if-then" rules (Boolean implications) mined from large-scale microarray databases. MiDReG uses two gene expression-based seed conditions that mark the initial and the terminal stages of a given differentiation pathway and combines the statistically inferred Boolean implications from these seed conditions to identify the relevant genes. The method was validated by applying it to B-cell development. The algorithm predicted 62 genes that are expressed after the KIT+ progenitor cell stage and remain expressed through CD19+ and AICDA+ germinal center B cells. qRT-PCR of 14 of these genes on sorted B-cell progenitors confirmed that the expression of 10 genes is indeed stably established during B-cell differentiation. Review of the published literature of knockout mice revealed that of the predicted genes, 63.4% have defects in B-cell differentiation and function and 22% have a role in the B cell according to other experiments, and the remaining 14.6% are not characterized. Therefore, our method identified novel gene candidates for future examination of their role in B-cell development. These data demonstrate the power of MiDReG in predicting functionally important intermediate genes in a given developmental pathway that is defined by a mutually exclusive gene expression pattern.|*Gene Expression Regulation, Developmental[MESH]|AICDA (Activation-Induced Cytidine Deaminase)[MESH]|Algorithms[MESH]|Animals[MESH]|Antigens, CD19/genetics[MESH]|Cell Differentiation/*genetics[MESH]|Computational Biology[MESH]|Cytidine Deaminase/genetics[MESH]|Data Mining/statistics & numerical data[MESH]|Databases, Genetic[MESH]|Gene Expression Profiling/statistics & numerical data[MESH]|Humans[MESH]|Mice[MESH]|Models, Statistical[MESH]|Oligonucleotide Array Sequence Analysis/statistics & numerical data[MESH]|Precursor Cells, B-Lymphoid/cytology/metabolism[MESH]|Stem Cell Factor/genetics[MESH] |