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The completion of the Human Genome Project and development in technologies
and techniques like ONCOMINE a joint venture between IOB and Chinnaiyan
Lab, Michigan University, is a bioinformatics infrastructure for
the cancer biologist where publicly available cancer microarray
studies are curated and provided with data mining tools to efficiently
query genes and expression profiles of interest as well as meta-analyze
groups of studies. The project has three modules in it (i) Query
by Gene, (ii) Query by Analysis and (iii) Meta Analysis.
Query by Gene: This module enables the user to query the data by
gene, using any one of the gene identifiers like Gene name/Symbol,
Swissprot ID, Unigene ID, Locus Link ID, OMIM ID with two flexible
search modes.
Quick search - This search mode is for the user not very familiar
to search engines and might find difficulties in trying to extract
a filtered output from the data set by using intelligent keyword
search. Hence, by default, the keyword entry is treated as an 'exact
match'. If the dataset does not give an exact match, then an automated
internal query is triggered to provide other possible combinations
of results.
Advanced search -This search mode is for the user with average exposure
to search tools. Here the user can select keywords with a range
of options like - start with, end with, exact match or contains
the keyword, without the use of wildcard characters. |
| Query by Analysis:
Multiple genes included in a particular study of interest can be
retrieved by the user by selecting a specific tissue (e.g. breast,
pancreas etc.). This dynamically updates the “Study”
option which provides the user with all the studies in the dataset
included for this specific tissue. The differential conditions (normal
versus diseased) under which the micro-array analysis was performed
can be chosen from the option “Class 1 vs Class 2”.
The retrieved results can be further filtered using ‘drug
target’ or ‘gene ontology’ as criteria. The display
parameters like Cell Width, Cell Height, Gene/Frame enable customizing
the result sets.
Meta Analysis: The Meta Module is useful for exploring selected
multi-study analyses that we have performed. Thus far, 5 such analyses
have been performed. First, we identified genes that are significantly
over-expressed in multiple cancers vs. normal analyses, a so called
universal cancer meta-profile. We found a large set of genes that
are highly expressed in many cancer types, suggesting an important
role in the process of carcinogenesis in general. Second, we defined
a high grade, or undifferentiated, meta profile, demonstrating that
high grade cancers share transcriptional features regardless of
cancer type. Third, we generated cancer type specific meta-profiles
for cancer types in which multiple analyses tested the same hypothesis
(e.g. prostate cancer vs. normal prostate). These meta-profiles
serve to cross-validate multiple studies. |
| Features:
Result set display options:
The output data obtained from the query search can be plotted using
either the bar graph or box plot options to assist further analysis.
The user can view this data for a single study or a group, by selecting
the appropriate check boxes. The image plots are supplemented by
detailed mouse-over descriptions to assist the user in comprehending
the plots. The image scale with reference to both width and height
can be changed choosing the variable parameters thus simulating
zooming features. The user can effortlessly toggle between the expression
data and the annotations for a specific gene using convenient hyper
links.
Download:
The download features (both types of graphs and data) are available
for all. |
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