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In the field of molecular biology, gene expression profiling is the measurement of the activity (the expression) of thousands of genes at once, to create a global picture of cellular function. These profiles can, for example, distinguish between cells that are actively dividing, or show how the cells react to a particular treatment.
Due to the biological complexity of gene expression, the considerations of experimental design that are discussed in the expression profiling article are of critical importance if statistically and biologically valid conclusions are to be drawn from the data. There are three main elements to consider when designing a microarray experiment.
Genes and samples with similar expression profiles can be automatically grouped (left and top trees). Samples may be different individuals, tissues, environments or health conditions. In this example, expression of gene set 1 is high and expression of gene set 2 is low in samples 1, 2, and 3. [51] [129]
It is currently one of the main methods, along with REAP-Seq, to evaluate both gene expression and protein levels simultaneously in different species. The method was established by the New York Genome Center in collaboration with the Satija lab ., [ 2 ] while a similar approach was earlier shown by AbVitro Inc. .
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The concept of gene co-expression networks was first introduced by Butte and Kohane in 1999 as relevance networks. [6] They gathered the measurement data of medical laboratory tests (e.g. hemoglobin level ) for a number of patients and they calculated the Pearson correlation between the results for each pair of tests and the pairs of tests which showed a correlation higher than a certain level ...
More recently, genome-wide screens to identify imprinted genes have used differential expression of mRNAs from control fetuses and parthenogenetic or androgenetic fetuses hybridized to gene expression profiling microarrays, [41] allele-specific gene expression using SNP genotyping microarrays, [42] transcriptome sequencing, [43] and in silico ...
Another study applying the cellular deconvolution algorithms to gene expression data of Alzheimer's patients find that patients with lower proportions of neuronal cells in the samples collected from their cerebral cortex are more likely to show the clinical characteristics of dementia. [44]