|
|
| |
|
| TGFR
Pathway |
 |
| |
| 
|
|
| |
 |
First of its kind, a database hosting over 6000 human proteins
and disease genes. The main objective of this database is
to make available all related fields of a protein including
Interactions, Post Translational Modifications, Substrates
and other information so as to help the scientists working
in the areas of Proteomics. This makes HPRD a reliable source
for protein data. HPRD will be the first ever database to
implement the standardization protocol put forward by the
Proteomics Standards Initiative for molecular interactions
(PSI MI). The annotations are manually done by scientists
working at IOB and each annotation undergoes multiple levels
of reviews before being made publicly available, to ensure
the quality. The plans are to complete 10000 proteins by the
end of April 2004.

|
|
| |
 |
Involves a careful and comprehensive analysis of Human 'X'
chromosome. Using comparative genomic approach, we have identified
novel protein coding regions; we have performed an extensive
pseudogene analysis of the 'X' chromosome and have documented
alternative splicing events. In order to help the scientific
community working on X-Linked Mental Retardation, the domain
is linked to HPRD where the user can view the annotations
of all the genes on 'X'.

|
|
| |
 |
A database which contains all the “Known molecular
alterations related to Breast Cancer”. This database
comprises of information related to known molecular alterations
at the chromosome, mRNA and protein levels. The database will
also comprise all the SAGE analysis and Microarray data relevant
to breast cancer. The data includes information on regulation
(up/down) of all the reported genes and its proteins related
to breast cancer. This database is linked to the HPRD for
manually curated protein annotations, ONCOMINE, Geneontology,
Unigene, and Genecard, where the user can have a comparative
account of cancerous and normal state for a particular gene
of their interest.

|
|
| |
 |
A thorough analysis of the protein tyrosine phosphatases
encoded by the human genome using computational biology methods.
Primary aim of the study is to identify novel tyrosine phosphatases
and novel transcript variants for all the known protein tyrosine
phosphatases. The findings are then experimentally validated
by experts using techniques such as RT-PCRs and Northern blots.

|
|
| |
 |
IOB in collaboration with Chinnaiyan Lab has created a microarray
database whose goal is to curate publicly available cancer
microarray studies and provide data mining tools to generate
biologically relevant information in a user friendly manner.
Links to various bioinformatics resources have been implemented
including Unigene, Swissprot, Biocarta, HPRD, and KEGG, among
others. IOB was involved in implementing the technical aspect
for the database and Chinnaiyan Lab provided the normalized
expression data. This database has been published in January/February
issue of Neoplasia.

|
|
| |
|
TOP |
|
 |
|
| |
 |
A content management system, designed for easy modifications
and management of HPRD using web interface. The administration
of annotation process and the multi-level review carried out
round the globe is made easy by the implementation of this
tool. This user friendly tool is created using Python and
Zope.

|
|
| |
 |
An application which would comprise the basic sequence data
along with the higher-level, location-based annotations on
the sequence: These annotations would relate the sequence
data to various genomic aspects like SNPs and expression profiling
data such as that derived from DNA microarray and SAGE studies
and also mass spectrometry derived data in order to understand
various post translational modifications. This would add value
to the analysis of the genomic sequence, as it would provide
several different contexts in which to interpret the genomic/transcriptomic/proteomic
data. With this application, when exploring a genomic region,
biologists would be able to interact with the interface in
a richer fashion than is currently possible using simple,
hyperlinked images.

|
|
| |
 |
Is a comprehensive tool used to perform tag-to-gene mapping.
The 10 base pair sequences of each of the SAGE tags, which
are generated experimentally in the lab, are submitted to
the tool as input. The output results in mapping the SAGE
tags to their respective genes by performing an extensive
search across the ‘dbEST’ and ‘non redundant’
database.

|
|
| |
|
TOP |
|
 |
|
| |
 |
Through comparative genomics approach we have predicted several
novel genes, which we are experimentally verifying in our
laboratory. Identification, isolation and characterization
of the predicted novel genes are the ultimate goals are being
accomplish by a variety of molecular biological techniques.
RT-PCR and Northern blot experiments are being performed to
validate the predicted genes and RNAi experiments are being
planned to check their function.
|
|
| |
 |
IOB has kept in pace with tremendous advances in proteomics,
a powerful tool to unravel the protein machinery of the cell.
Understanding the complexities of proteomics such as protein
structure, function, protein-protein interaction, sub cellular
localization and post-translational modifications is facilitated
because of the availability of completely sequenced human
genome and the use of high through-put mass spectrometry technology.
We are employing the recent strategies of quantitative protein
profiling in different biological systems delivering more
insights into the human health and diseases. Our proteomics
experiments are also intended to complement the findings of
microarray analysis and comparative genomics, which are underway
at IOB.
|
|
| |
 |
|
| |
 |
|
| |
TOP |
|