Conclusions-Computer Science-Project Presentation, Slides of Computer Science

This is project presentation for computer science degree. This project was supervised by Dr. Niharika Raj at Acharya Nagarjuna University. Its main topics are: Conclulsion, Computer, Project, Results, Methods, GP, KNN, Measure, Phase, Protein, Learning, Technique

Typology: Slides

2011/2012

Uploaded on 07/16/2012

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5-fold Cross-validation
Methods GP KNN Fuzzy KNN
Accuracy MCC K Accuracy MCC K Accuracy MCC
DS2
AAC
PseAAC
SAAC
AAC+ PseAAC
AAC+SAAC
PseAAC +SAAC
AAC+ PseAAC +SAAC
94.33
92.01
93.94
92.39
94.84
93.04
94.45
0.72
0.60
0.71
0.63
0.76
0.66
0.72
3
3
9
3
3
3
3
96.36
96.39
96.78
96.26
96.13
96.65
96.13
0.83
0.83
0.85
0.82
0.81
0.84
0.81
5
5
5
5
5
5
5
99.39
99.35
99.55
99.39
99.40
99.39
99.39
0.95
0.94
0.96
0.95
0.95
0.95
0.94
RESULTS
96
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96

5-fold Cross-validation

Methods

GP
KNN

Fuzzy KNN

Accuracy

MCC
K

Accuracy

MCC
K

Accuracy

MCC
DS

AACPseAACSAACAAC+ PseAACAAC+SAACPseAAC +SAACAAC+ PseAAC +SAAC

RESULTS

96

Prediction performance of Fuzzy KNN

5-fold Cross-validation

Measures

OMPs vs. Globular

K=

OMPs vs. alpha-helix

K=

OMPs vs. Non-OMPs

K=
DS

AccuracySensitivitySpecificityMCC

DS

AccuracySensitivitySpecificityMCC

97

RESULTS

97

Comparative analysis between the proposed approach and existing approaches on

DS

99

Measures

Yan et al. [15]

Yan et al. [15]

Mizianty et al. [18]

Proposed Method

OMPs vs. Non-OMPs

AccuracySensitivitySpecificityMCC

RESULTS

99

CONCLUSIONS

100

C

ONCLUSIONS AND

F

UTURE

W

ORK

Our research finding revealed that computational methods formembrane proteins prediction are efficient and fast.

Research in pharmaceutical industry might be accelerated throughcomputational methods

Our research might be useful for protein structure prediction anddrugs discovery

Due to the complex nature and limited availability of membraneprotein structure, it should be the spotlight of future researchwork in the Machine learning community

102

A

CKNOWLEDGEMENTS

Pattern Recognition Lab, DCIS, Pakistan Institute ofEngineering and Applied Sciences Islamabad

Higher Education Commission, Pakistan

Center for Biophysics and Computational Biology, BeckmanInstitute, University of Illinois, USA

103

REFERENCES

Zumdahi, S., 2000. Chemistry5th edition Houghton Mifflin Company

Waugh, D.F., 1954. Protein–Protein interactions. Adv. Protein Chem. 9, 325–437.

Eisenberg, D., Schwarz, E., Komaromy, M.,Wall, R., 1984. Analysis ofmembrane and surface protein sequences with the hydrophobic momentplot. J. Mol. Biol. 179, 125–142.

Chou, K.C., Cai, Y.D., 2005. Prediction of

membrane protein types by

incorporating amphipathic effects. J. Chem. Inf. Model 45, 407–413.

Chou, K.C., Shen, H.S., 2007. MemType-2L: a web server for predictingmembrane proteins and their types by incorporating evolution informationthrough Pse-PSSM. Biochem. Biophys. Res. Commun. 360, 339–345.

A. Mahdavi, and S. Jahandideh, Application of density similarities to predictmembrane protein types based on pseudo-amino acid composition. Journalof Theoretical Biology 276 (2011) 132-137.

105

REFERENCES

Sklar, B., 2001. Digital Communications: Fundamentals and Applications.Prentice- Hall Inc.

Moller, S.; Kriventseva, E. V.; Apweiler, R. A collection of well characterizedintegral membrane proteins. Bioinformatics 2000, 16 (12), 1159–60.

Ikeda,

M.;

Arai,

M.;

Okuno,

T.;

Shimizu,

T.

TMPDB:

a

database

of

experimentally-characterized transmembrane topologies. Nucleic Acids Res.2003, 31 (1), 406–

Yan, C.; Hu, J., and Wang, Y. Discrimination of outer membrane proteinswith improved performance. BMC Bioinformatics 9 (2008) 47.

Park, K.J.; Gromiha, M.M.; Horton, P.; and Suwa, M. Discrimination ofouter Membrane proteins using support vector machines.. Bioinformatics 21(2005) 4223–4229.

106

THANK

Y

U

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