2,967 research outputs found
Uncertainty quantification in energy management procedures
Complex energy systems are made up of a number of components interacting together via different energy vectors. The assessment of their performance under dynamic working conditions, where user demand and energy prices vary over time, requires a simulation tool. Regardless of the accuracy of this procedure, the uncertainty in data, obtained both by measurements or by forecasting, is usually non-negligible and requires the study of the sensitivity of results versus input data. In this work, polynomial chaos expansion technique is used to evaluate the variation of cogeneration plant performance with respect to the uncertainty of energy prices and user requests. The procedure allows to obtain this information with a much lower computational cost than that of usual Monte-Carlo approaches. Furthermore, all the tools used in this paper, which were developed in Python, are published as free and open source software
Energy networks in sustainable cities: Polycity project and the case study of Turin – Arquata
Design Considerations for Efficient and Effective Microarray Studies
This paper describes the theoretical and practical issues in experimental design for gene expression microarrays. Specifically, this paper (1) discusses the basic principles of design (randomization, replication, and blocking) as they pertain to microarrays, and (2) provides some general guidelines for statisticians designing microarray studies
Energy networks in sustainable cities: towards a lull integration of renewable systems in urban area
Assessment of resistance mechanisms and clinical implications in patients with kras mutated-metastatic breast cancer and resistance to cdk4/6 inhibitors
Simple SummaryPalbociclib in combination with fulvestrant is used globally to treat metastatic breast cancer, but it was recognized that not all patients benefit from this combination of drugs. However, the predictive factors remain unknown. Here, we show KRAS ctDNA levels as predictive mechanisms of resistance to palbociclib and fulvestrant, and their association with the time to treatment discontinuation of the above treatment. These observations shed light on the potential clinical applications of ctDNA analysis in this setting of patients, in order to provide critical information about tumour dynamics, and to predict who will take advantage from CDK4/6 inhibitors.Despite therapeutic improvements, resistance to palbociclib is a growing clinical challenge which is poorly understood. This study was conducted in order to understand the molecular mechanisms of resistance to palbociclib, and to identify biomarkers to predict who will take advantage from cyclin-dependent kinase 4/6 inhibitors (CDK4/6i). A total of about a thousand blood samples were collected from 106 patients with hormone receptor positive (HR+) human epidermal growth factor receptor 2 (HER2) negative metastatic breast cancer who received palbociclib in combination with fulvestrant as the first-line metastatic therapy enrolled in this study. The genotyping of their plasma cell-free DNA was studied, including serial plasma samples. Collectively, our findings identify the appearance of KRAS mutations leading to palbociclib resistance acquisition within 6 months, and provide critical information for the prediction of therapeutic responses in metastatic breast cancer. By monitoring KRAS status through liquid biopsy, we could predict who will take advantage from the combination of palbociclib and fulvestrant, offering highly-individualized treatment plans, thus ensuring the best patient quality of life
The Iterative Signature Algorithm for the analysis of large scale gene expression data
We present a new approach for the analysis of genome-wide expression data.
Our method is designed to overcome the limitations of traditional techniques,
when applied to large-scale data. Rather than alloting each gene to a single
cluster, we assign both genes and conditions to context-dependent and
potentially overlapping transcription modules. We provide a rigorous definition
of a transcription module as the object to be retrieved from the expression
data. An efficient algorithm, that searches for the modules encoded in the data
by iteratively refining sets of genes and conditions until they match this
definition, is established. Each iteration involves a linear map, induced by
the normalized expression matrix, followed by the application of a threshold
function. We argue that our method is in fact a generalization of Singular
Value Decomposition, which corresponds to the special case where no threshold
is applied. We show analytically that for noisy expression data our approach
leads to better classification due to the implementation of the threshold. This
result is confirmed by numerical analyses based on in-silico expression data.
We discuss briefly results obtained by applying our algorithm to expression
data from the yeast S. cerevisiae.Comment: Latex, 36 pages, 8 figure
DI-(2- ETHYLHEXYL) phthalate metabolites in urine show age-related changes and associations with adiposity and parameters of insulin sensitivity in chilhood.
Di-(2-ethylhexyl) phthalate metabolites in urine show age-related changes and associations with adiposity and parameters of insulin sensitivity in childhood
Objectives: Phthalates might be implicated with obesity and insulin sensitivity. We evaluated the levels of primary and secondary metabolites of Di-(2-ethylhexyl) phthalate (DEHP) in urine in obese and normal-weight subjects both before and during puberty, and investigated their relationships with auxological parameters and indexes of insulin sensitivity. Design and Methods: DEHP metabolites (MEHP, 6-OH-MEHP, 5-oxo-MEHP, 5-OH-MEHP, and 5-CX-MEHP), were measured in urine by RP-HPLC-ESI-MS. Traditional statistical analysis and a data mining analysis using the Auto-CM analysis were able to offer an insight into the complex biological connections between the studied variables. Results: The data showed changes in DEHP metabolites in urine related with obesity, puberty, and presence of insulin resistance. Changes in urine metabolites were related with age, height and weight, waist circumference and waist to height ratio, thus to fat distribution. In addition, clear relationships in both obese and normal-weight subjects were detected among MEHP, its products of oxidation and measurements of insulin sensitivity. Conclusion: It remains to be elucidated whether exposure to phthalates per se is actually the risk factor or if the ability of the body to metabolize phthalates is actually the key point. Further studies that span from conception to elderly subjects besides further understanding of DEHP metabolism are warranted to clarify these aspects
Di-(2-Ethylhexyl) Phthalate Metabolites in Urine Show Age-Related Changes and Associations with Adiposity and Parameters of Insulin Sensitivity in Childhood.
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