HIV drug resistance analysis tool based on process algebra
被引:0
|
作者:
de Araujo, Luciano Vieira
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机构:
Univ Sao Paulo, Dept Bioinformat, Rua Matao 1010, BR-05508009 Sao Paulo, BrazilUniv Sao Paulo, Dept Bioinformat, Rua Matao 1010, BR-05508009 Sao Paulo, Brazil
de Araujo, Luciano Vieira
[1
]
Sabino, Ester C.
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机构:
Univ Sao Paulo, Fundacao Prosangue, Sao Paulo, BrazilUniv Sao Paulo, Dept Bioinformat, Rua Matao 1010, BR-05508009 Sao Paulo, Brazil
Sabino, Ester C.
[2
]
Ferreira, Joao Eduardo
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机构:
Univ Sao Paulo, Dept Comp Sci, Sao Paulo, BrazilUniv Sao Paulo, Dept Bioinformat, Rua Matao 1010, BR-05508009 Sao Paulo, Brazil
Ferreira, Joao Eduardo
[3
]
机构:
[1] Univ Sao Paulo, Dept Bioinformat, Rua Matao 1010, BR-05508009 Sao Paulo, Brazil
[2] Univ Sao Paulo, Fundacao Prosangue, Sao Paulo, Brazil
[3] Univ Sao Paulo, Dept Comp Sci, Sao Paulo, Brazil
Process Algebra;
Drug Resistance;
HIV;
NPDL;
Mutation Analysis;
Genotypic Drug Resistance Testing;
D O I:
暂无
中图分类号:
TP39 [计算机的应用];
学科分类号:
081203 ;
0835 ;
摘要:
The increasing number of drugs used in HIV patient treatment and the mutations associated with drug resistance make the inference of drug resistance a complex task that demands computational systems. Furthermore, the software development/update can generate an extra level of complexity in the process drug resistance analysis. An alternative to handle the complexity of drug resistance and software development is to use a formal representation of involved processes, such as process algebra. This allows mathematical reasoning about the analysis process, a precise description of system behavior, more advanced computational approaches, as concurrent/parallel execution and (semi) automatic software development. The first contribution of this research is a mapping of drug resistance algorithms rules into expressions of process algebra which facilitates the computational manipulation of theses rules. The second contribution is the HIVdag (HIV Drug Analysis Generator) system. This software supports the definition, generation and analyses of genotypic drug resistance tests based on process algebra expressions. Therefore, the users can easily create/update their own drug resistance algorithms any time and independent of software development.
机构:
Minist Hlth & Social Dev, DI Ivanovsky Inst Virol, T Lymphotrop Viruses Lab, Moscow, RussiaMinist Hlth & Social Dev, DI Ivanovsky Inst Virol, T Lymphotrop Viruses Lab, Moscow, Russia
Lapovok, I
Laga, V
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Minist Hlth & Social Dev, DI Ivanovsky Inst Virol, T Lymphotrop Viruses Lab, Moscow, RussiaMinist Hlth & Social Dev, DI Ivanovsky Inst Virol, T Lymphotrop Viruses Lab, Moscow, Russia
Laga, V
Vasilyev, A.
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Minist Hlth & Social Dev, DI Ivanovsky Inst Virol, T Lymphotrop Viruses Lab, Moscow, RussiaMinist Hlth & Social Dev, DI Ivanovsky Inst Virol, T Lymphotrop Viruses Lab, Moscow, Russia
Vasilyev, A.
Kazennova, E.
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机构:
Minist Hlth & Social Dev, DI Ivanovsky Inst Virol, T Lymphotrop Viruses Lab, Moscow, RussiaMinist Hlth & Social Dev, DI Ivanovsky Inst Virol, T Lymphotrop Viruses Lab, Moscow, Russia
Kazennova, E.
Ludvikova, E.
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机构:
Kazakh Republ Ctr AIDS Prevent & Control, Alma Ata, KazakhstanMinist Hlth & Social Dev, DI Ivanovsky Inst Virol, T Lymphotrop Viruses Lab, Moscow, Russia
Ludvikova, E.
Kovtunenko, N.
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机构:
Kazakh Republ Ctr AIDS Prevent & Control, Alma Ata, KazakhstanMinist Hlth & Social Dev, DI Ivanovsky Inst Virol, T Lymphotrop Viruses Lab, Moscow, Russia
Kovtunenko, N.
Dzisyuk, N.
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机构:
Kazakh Republ Ctr AIDS Prevent & Control, Alma Ata, KazakhstanMinist Hlth & Social Dev, DI Ivanovsky Inst Virol, T Lymphotrop Viruses Lab, Moscow, Russia
Dzisyuk, N.
Tukeev, M.
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机构:
Kazakh Republ Ctr AIDS Prevent & Control, Alma Ata, KazakhstanMinist Hlth & Social Dev, DI Ivanovsky Inst Virol, T Lymphotrop Viruses Lab, Moscow, Russia
Tukeev, M.
Bobkova, M.
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机构:
Minist Hlth & Social Dev, DI Ivanovsky Inst Virol, T Lymphotrop Viruses Lab, Moscow, RussiaMinist Hlth & Social Dev, DI Ivanovsky Inst Virol, T Lymphotrop Viruses Lab, Moscow, Russia