Datasets in Bioinformatics
From DrugPedia: A Wikipedia for Drug discovery
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'''Dataset''' | '''Dataset''' | ||
- | Here is two datasets that are used in developing this server is : [http://www.imtech.res.in/raghava/propred1/matrices/hla-a2.html/ HLA-A*0201] | + | Here is two datasets that are used in developing this server is : |
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+ | [http://www.imtech.res.in/raghava/propred1/matrices/hla-a2.html/ HLA-A*0201] | ||
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[http://www.imtech.res.in/raghava/propred1/matrices/h2kb.html/ H2-kb] | [http://www.imtech.res.in/raghava/propred1/matrices/h2kb.html/ H2-kb] | ||
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+ | ==Matrix Optimization Technique for Predicting MHC binding Core== | ||
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+ | The X-ray crystal structure of MHC class II molecule has revealed open peptide binding groove. A peptide bound in this groove may flank from one or the other side. Understanding which residues are acctually involved in binding will be very useful for understanding MHC peptide interactios.Here Matrix Optimization Technique is used to predict MHC binding core. Using binders from MHCPEP and nonbinder Data with MOT an accuracy of correct classification from 97 to 99% was obtained with HLA-DR1, HLA-DR2 and HLA-DR5 allele. This is the highest accuracy reported by any method. The prediction method used in this server is based on MOT and relies on the thought that binders have unique patterns which can be easily distinguished from nonbinders. | ||
+ | |||
+ | '''Dataset''' | ||
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+ | The "Binder" used in this study : | ||
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+ | [http://www.imtech.res.in/raghava/mhc/dr1bin.html/ HLA-DR1] | ||
+ | |||
+ | [http://www.imtech.res.in/raghava/mhc/dr2bin.html/ HLA-DR2] | ||
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+ | [http://www.imtech.res.in/raghava/mhc/dr5bin.html/ HLA-DR5] | ||
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+ | The "Non-binder" used in this study are : | ||
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+ | [http://www.imtech.res.in/raghava/mhc/dr1nonbin.html/ HLA-DR1] | ||
+ | |||
+ | [http://www.imtech.res.in/raghava/mhc/dr2nonbin.html/ HLA-DR2] | ||
+ | |||
+ | [http://www.imtech.res.in/raghava/mhc/dr5nonbin.html/ HLA-DR] |
Revision as of 09:15, 3 September 2008
There are a number of Datasets that are being created and used in the field of Bioinformatics. Datasets contains the vital information based on which a prediction server depends for it's function. here is some of the datasets that are being created or used by Bioinformatics Centre, Institute of Microbiology, Chandigarh are as follows :
Datasets for evaluation of beta turn prediction method
The dataset has 426 non-homologus protein chains. In this data set, no two protein chains have more than 25% sequence identity.The structure of these proteins is determined by X-ray crystallography at 2.0 resolution or better. Each chain contains minimum one beta turn.
Complete Dataset
- Amino acid sequence of 426 protein chains in fasta format
ProPred-I
The Promiscuous MHC Class-I Binding Peptide Prediction Server
The ProPred-I is an on-line service for identifying the MHC Class-I binding regions in antigens. It implements matrices for 47 MHC Class-I alleles, proteasomal and immunoproteasomal models. The main aim of this server is to help users in identifying the promiscuous regions.
Dataset
Here is two datasets that are used in developing this server is :
Matrix Optimization Technique for Predicting MHC binding Core
The X-ray crystal structure of MHC class II molecule has revealed open peptide binding groove. A peptide bound in this groove may flank from one or the other side. Understanding which residues are acctually involved in binding will be very useful for understanding MHC peptide interactios.Here Matrix Optimization Technique is used to predict MHC binding core. Using binders from MHCPEP and nonbinder Data with MOT an accuracy of correct classification from 97 to 99% was obtained with HLA-DR1, HLA-DR2 and HLA-DR5 allele. This is the highest accuracy reported by any method. The prediction method used in this server is based on MOT and relies on the thought that binders have unique patterns which can be easily distinguished from nonbinders.
Dataset
The "Binder" used in this study :
The "Non-binder" used in this study are :