scholarly journals Study on Driving Cycle Synthesis Method for City Buses considering Random Passenger Load

2020 ◽  
Vol 2020 ◽  
pp. 1-21 ◽  
Author(s):  
Xiaodong Liu ◽  
Jian Ma ◽  
Xuan Zhao ◽  
Juan Du ◽  
Yanfeng Xiong

This paper proposes a novel driving cycle construction method in consideration of velocity, road slope, and passenger load, based on a real-world bus route with a plug-in hybrid electric bus (PHEB). The main purpose is to address the disadvantage that an inaccurate reflection of the real-world driving characteristics for city buses will be caused when ignoring the passenger load in the course of a driving cycle synthesis. Two contributions are supplemented to distinguish from the previous research. Firstly, a novel station-based method is proposed aiming at developing a driving cycle with high accuracy. The kinematic segments are partitioned according to the distance of adjacent bus stops, while a two-dimensional Markov chain Monte Carlo method is employed to synthesize driving cycle between each interval of adjacent bus stops. Secondly, the random passenger load for different bus stops is treated as a discrete Markov chain model, according to the correlation analysis of the measured passenger data which are distinguished for off-peak and peak hours. Meanwhile, Monte Carlo simulation and maximum likelihood estimation are utilized to determine the most likely number of passengers for each bus stop. At last, the fuel consumption of the PHEB is simulated with the best-synthesized driving cycle and contrasted to the mean fuel consumption of the later measured data which is composed of the velocity, road slope, and the passenger load. The results demonstrate that the synthesized driving cycle has a higher accuracy on fuel consumption estimation.

2019 ◽  
Vol 80 (3) ◽  
pp. 545-573 ◽  
Author(s):  
Fred Vermolen ◽  
Ilkka Pölönen

AbstractA spatial Markov-chain model is formulated for the progression of skin cancer. The model is based on the division of the computational domain into nodal points, that can be in a binary state: either in ‘cancer state’ or in ‘non-cancer state’. The model assigns probabilities for the non-reversible transition from ‘non-cancer’ state to the ‘cancer state’ that depend on the states of the neighbouring nodes. The likelihood of transition further depends on the life burden intensity of the UV-rays that the skin is exposed to. The probabilistic nature of the process and the uncertainty in the input data is assessed by the use of Monte Carlo simulations. A good fit between experiments on mice and our model has been obtained.


2004 ◽  
Vol 68 (2) ◽  
pp. 346 ◽  
Author(s):  
Keijan Wu ◽  
Naoise Nunan ◽  
John W. Crawford ◽  
Iain M. Young ◽  
Karl Ritz

Author(s):  
R. Jamuna

CpG islands (CGIs) play a vital role in genome analysis as genomic markers.  Identification of the CpG pair has contributed not only to the prediction of promoters but also to the understanding of the epigenetic causes of cancer. In the human genome [1] wherever the dinucleotides CG occurs the C nucleotide (cytosine) undergoes chemical modifications. There is a relatively high probability of this modification that mutates C into a T. For biologically important reasons the mutation modification process is suppressed in short stretches of the genome, such as ‘start’ regions. In these regions [2] predominant CpG dinucleotides are found than elsewhere. Such regions are called CpG islands. DNA methylation is an effective means by which gene expression is silenced. In normal cells, DNA methylation functions to prevent the expression of imprinted and inactive X chromosome genes. In cancerous cells, DNA methylation inactivates tumor-suppressor genes, as well as DNA repair genes, can disrupt cell-cycle regulation. The most current methods for identifying CGIs suffered from various limitations and involved a lot of human interventions. This paper gives an easy searching technique with data mining of Markov Chain in genes. Markov chain model has been applied to study the probability of occurrence of C-G pair in the given   gene sequence. Maximum Likelihood estimators for the transition probabilities for each model and analgously for the  model has been developed and log odds ratio that is calculated estimates the presence or absence of CpG is lands in the given gene which brings in many  facts for the cancer detection in human genome.


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