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1.
Singapore medical journal ; : 59-66, 2023.
Artigo em Inglês | WPRIM | ID: wpr-969666

RESUMO

Advancements in high-throughput sequencing have yielded vast amounts of genomic data, which are studied using genome-wide association study (GWAS)/phenome-wide association study (PheWAS) methods to identify associations between the genotype and phenotype. The associated findings have contributed to pharmacogenomics and improved clinical decision support at the point of care in many healthcare systems. However, the accumulation of genomic data from sequencing and clinical data from electronic health records (EHRs) poses significant challenges for data scientists. Following the rise of artificial intelligence (AI) technology such as machine learning and deep learning, an increasing number of GWAS/PheWAS studies have successfully leveraged this technology to overcome the aforementioned challenges. In this review, we focus on the application of data science and AI technology in three areas, including risk prediction and identification of causal single-nucleotide polymorphisms, EHR-based phenotyping and CRISPR guide RNA design. Additionally, we highlight a few emerging AI technologies, such as transfer learning and multi-view learning, which will or have started to benefit genomic studies.


Assuntos
Inteligência Artificial , Ciência de Dados , Estudo de Associação Genômica Ampla , Genômica , Tecnologia
2.
Biol. Res ; 48: 1-6, 2015. ilus, tab
Artigo em Inglês | LILACS | ID: biblio-950786

RESUMO

BACKGROUND: Pseudomonas aeruginosa is known to be a multidrug resistant opportunistic pathogen. Particularly, P. aeruginosa PAO1 polyphosphate kinase mutant (ppk1) is deficient in motility, quorum sensing, biofilm formation and virulence. FINDINGS: By using Phenotypic Microarrays (PM) we analyzed near 2000 phenotypes of P. aeruginosa PAO1 polyP kinase mutants (ppk1 and ppk2). We found that both ppk mutants shared most of the phenotypic changes and interestingly many of them related to susceptibility toward numerous and different type of antibiotics such as Ciprofloxacin, Chloramphenicol and Rifampicin. CONCLUSIONS: Combining the fact that ppk1 mutants have reduced virulence and are more susceptible to antibiotics, polyP synthesis and particularly PPK1, is a good target for the design of molecules with anti-virulence and anti-persistence properties.


Assuntos
Pseudomonas aeruginosa/enzimologia , Fosfotransferases (Aceptor do Grupo Fosfato)/genética , Farmacorresistência Bacteriana Múltipla/genética , Análise em Microsséries/métodos , Mutação , Fenótipo , Polifosfatos/metabolismo , Pseudomonas aeruginosa/efeitos dos fármacos , Pseudomonas aeruginosa/patogenicidade , Rifampina/farmacologia , Virulência/genética , Ciprofloxacina/farmacologia , Cloranfenicol/farmacologia , Antibacterianos/farmacologia
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