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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.

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PathBuilder is an open source software to annotate biological information pertaining to signaling pathways and, with minimal additional effort, to create web-based pathway resources. PathBuilder enables annotation of molecular events including protein-protein interactions, enzyme-substrate relationships and protein translocation events via manual or automatic methods. The features of PathBuilder include automatic validation of data formats, built-in modules for visualizing pathways, automated import of data from other pathway resources, export of data in several standard data exchange formats and an application programming interface for retrieving pathway datasets.

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First of its kind, a database hosting over 25000 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 is 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 database host annotations of all the
known human proteins and update them on an ongoing basis.

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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.

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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.

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The Plasma Proteome Database, the first of its kind ensures a comprehensive resource for all human plasma proteins along with their isoforms. The database includes information pertaining to isoform specific expression, disease, localization, post translational modification and single nucleotide polymorphism. The information provided in this database is through manual annotation done by exhaustive literature research.

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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.

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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'.

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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.

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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.

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