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1.
Brief Bioinform ; 16(6): 964-73, 2015 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-25888697

RESUMO

De novo motif discovery is a difficult computational task. Historically, dedicated algorithms always reported a high percentage of false positives. Their performance did not improve considerably even after they adapted to handle large amounts of chromatin immunoprecipitation sequencing (ChIP-Seq) data. Several studies have advocated aggregating complementary algorithms, combining their predictions to increase the accuracy of the results. This led to the development of ensemble methods. To form a better view on modern ensembles, we review all compound tools designed for ChIP-Seq. After a brief introduction to basic algorithms and early ensembles, we describe the most recent tools. We highlight their limitations and strengths by presenting their architecture, the input options and their output. To provide guidance for next-generation sequencing practitioners, we observe the differences and similarities between them. Last but not least, we identify and recommend several features to be implemented by any novel ensemble algorithm.


Assuntos
Imunoprecipitação da Cromatina/métodos , Algoritmos
3.
Adv Sci (Weinh) ; 10(12): e2203485, 2023 04.
Artigo em Inglês | MEDLINE | ID: mdl-36808826

RESUMO

Chronic obstructive pulmonary disease (COPD) is one of the leading causes of death worldwide. Current COPD diagnosis (i.e., spirometry) could be unreliable because the test depends on an adequate effort from the tester and testee. Moreover, the early diagnosis of COPD is challenging. The authors address COPD detection by constructing two novel physiological signals datasets (4432 records from 54 patients in the WestRo COPD dataset and 13824 medical records from 534 patients in the WestRo Porti COPD dataset). The authors demonstrate their complex coupled fractal dynamical characteristics and perform a fractional-order dynamics deep learning analysis to diagnose COPD. The authors found that the fractional-order dynamical modeling can extract distinguishing signatures from the physiological signals across patients with all COPD stages-from stage 0 (healthy) to stage 4 (very severe). They use the fractional signatures to develop and train a deep neural network that predicts COPD stages based on the input features (such as thorax breathing effort, respiratory rate, or oxygen saturation). The authors show that the fractional dynamic deep learning model (FDDLM) achieves a COPD prediction accuracy of 98.66% and can serve as a robust alternative to spirometry. The FDDLM also has high accuracy when validated on a dataset with different physiological signals.


Assuntos
Aprendizado Profundo , Doença Pulmonar Obstrutiva Crônica , Humanos , Doença Pulmonar Obstrutiva Crônica/diagnóstico , Espirometria , Redes Neurais de Computação
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