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Biointerpreter User
Manual
NOTE: 75% of the microarray data is not avilable in Demo version.
Subscribe to the Full version
and get other advantages.
Biointerpreter
is an online tool with user friendly web interface. There is no special
training required to efficiently use the tool. Fill up the registration
form to obtain a or
Demo Login
purchase subscription. Visit
http://www.genotypic.co.in/bionterpreter_login.htm
to reach login page.
Login
Page

Your
email ID is the LoginID (not case sencitive), the password is case
sensitive. If the server is busy with other requests it will take up 10
seconds for logging into the program. If the login check internet
connection by visiting other sites. If you can reach other websites, try
logging again. Try logging into the
Demo server if the login fails repeatedly. If you are using
a Demo login, verify if you have exceeded the number of logins or the demo
period is completed. Email biointerpreter@genotypic.co.in
to obtain a new demo login or purchase a subscription.
Biointerpreter
Query page


Paste the Gene Ids into the text box
as shown below. The Ids should be separated by carriage return i.e. each
ID should be in a separate line.
Example Gene ids
1. Type the study name in the box provided. (Study name is for your
reference, it does not change the way program works.)
2.
Choose the P value cutoff (choose default value of 0.05 if you are doing the
search for the first search)
3.
Click on the Search button.
The
search time taken is 10 seconds to 30 seconds and might vary depending on the
number of IDs entered and the internet speed. Reduce the number of Ids if
the results page takes more than 2 minute to load. Biointerpreter
will search your gene identifiers in the comprehensive annotation database. It
will retrieve all the necessary annotation from the database. Then it will sort
out the results in to different category like functions, disease, pathway,
chromosome, etc.
The result will be
categorized in to following categories.
-
Summary report
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Chromosome
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Pathway Function
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Disease
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Localization
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Gene Expression
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Cancer Gene expression
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Protein domain
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Protein Ligand
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Tissue expression
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Gene Ontology
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Hot molecules
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Drug response
Biointerpreter
Results
Under
each category, there will be subcategory / elements. For example a list of
functions will be displayed under the function category. For each function, the
number of genes supporting the function, and P value will be given.
Biointerpreter counts the number of genes in the query list supporting each
function and will find the significance. A set of significant functions will be
retrieved and displayed. NOTE: Some categories are not available in the demo
version.

Summary
Report
Summary
report gives the following details
-
Study Name: The
study name entered by the user in the previous page.
-
ID type: The
type of ID queried by the user.
-
IDs Entered:
Number of ids you have pasted in the “Paste ids” textbox
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Non-redundant
Ids: If any id in the list is repeated, the redundancy will be removed. Only
the unique list of ids will be taken to query the database.
-
Number of genes
found: Number of genes found in the database for the IDs entered
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Number of ids
not found: Ids not found in the database.
-
The
resutl views can be exported to Excel sheet and can be saved in the
computer.

The
user can view the list of genes found in the database by clicking “Number of
Genes Found” button. It displays the genes found with symbols and gene
name. Unigene in this page is linked to detailed annotation of the
corresponding gene.
P
value:
P
value (Probability value) is the probability of getting the same result with a
random set of gene identifiers. Chi-square test is used to calculate the
P value. Chi-square is a common statistical method used to derive P value
of the (input) observed data and expected data. If the P value is about 0.10,
it means there is a 10% probability that the deviation is only due to chance
and other factors are involved. P value less than 0.05 considered as
significant. The results are sorted by P value in increasing order.
Viewing
the Resutl Categories & Interpretation
Example - Function
To
view the functions related to the
queried genes in the function table. The detailed function table is listed
below.

Biointerpreter
finds the list of functions that are over represented in query list. The
details are
To
view the genes involved in a function
-
Select the function by clicking the corresponding check box
-
click the "Table view" button
The
list of genes associated with fucntions selected will be displayed at the right
window with the following information:
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Query ID
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Unigene ID with link to detailed annotation
-
Gene name
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Gene Symbol
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Functions
To view genes
involved in all the selected functions:
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Select the Functions by clicking on
the corresponding check boxes.
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Select ‘AND’ radio button at the
bottom.
-
Click the ‘Table View’ button.

In
the above figure, the user would like to view the genes involved in both Angiogenesis
and Antigen Processing & Presentation. Biointerpreter finds
the genes involved in both of the functions and reports in the result window.

Number
of related keywords of the function found in the comprehensive annotation of
the gene is displayed under each function. This number is hyperlinked to get
detailed annotation of the gene. Related keywords for the function will be
highlighted in the detailed annotation.
For
example, in the above figure,
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2
related keywords of “Angiogenesis” were found in
Hs.109225.
-
2
related keywords of “Antigen processing and Presentation” were
found in Hs.111779.
-
If
you click on Angiogenesis found in Hs.109225 it will give you
detailed annotation for Hs.109225

To view genes
involved in any one of the selected functions:
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Select the
Functions by clicking on the corresponding check boxes
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Select
‘OR’ radio button at the bottom.
-
Click the
‘Table View’ button.
List of genes
involved in any one of the function will be displayed at the result window.
To
view the pie chart for the selected functions:

Adjust
the frames to your convenience

Hold
the frame divider (highlighted yellow in this figure)
and move right or left to increase the width of the desired frame.


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