New phase phenomena in ternary systems at high pressures – Cosolvency and miscibility windows up to 100 MPaElectronic supplementary information (ESI) available: tables of experimental data. See http://www.rsc.org/suppdata/cp/b1/b109224n/

2002 ◽  
Vol 4 (6) ◽  
pp. 963-967 ◽  
Author(s):  
Arndt L. Scheidgen ◽  
Gerhard M. Schneider
2021 ◽  
Vol 170 ◽  
pp. 105140
Author(s):  
Rogerio Favareto ◽  
Paulo Cardozo Carvalho de Araujo ◽  
Isaac Dias Bezerra ◽  
Andreia Fátima Zanette ◽  
Pedro Felipe Arce ◽  
...  

2021 ◽  
Vol 2057 (1) ◽  
pp. 012118
Author(s):  
K V Khishchenko

Abstract An equation of state has been developed for rhodium in a wide range of changes in the specific volume and internal energy. The results of calculations of the thermodynamic characteristics of this metal are presented in comparison with the available experimental data at high pressures. This equation of state can be used in the numerical simulation of hydrodynamic processes under intense impulse influences on matter.


2019 ◽  
Vol 35 (18) ◽  
pp. 3279-3286 ◽  
Author(s):  
Enrico Siragusa ◽  
Niina Haiminen ◽  
Richard Finkers ◽  
Richard Visser ◽  
Laxmi Parida

Abstract Summary Haplotype assembly of polyploids is an open issue in plant genomics. Recent experimental studies on highly heterozygous autotetraploid potato have shown that available methods do not deliver satisfying results in practice. We propose an optimal method to assemble haplotypes of highly heterozygous polyploids from Illumina short-sequencing reads. Our method is based on a generalization of the existing minimum fragment removal model to the polyploid case and on new integer linear programs to reconstruct optimal haplotypes. We validate our methods experimentally by means of a combined evaluation on simulated and experimental data based on 83 previously sequenced autotetraploid potato cultivars. Results on simulated data show that our methods produce highly accurate haplotype assemblies, while results on experimental data confirm a sensible improvement over the state of the art. Availability and implementation Executables for Linux at http://github.com/Computational Genomics/HaplotypeAssembler. Supplementary information Supplementary data are available at Bioinformatics online.


2019 ◽  
Vol 35 (18) ◽  
pp. 3378-3386 ◽  
Author(s):  
Marco S Nobile ◽  
Thalia Vlachou ◽  
Simone Spolaor ◽  
Daniela Bossi ◽  
Paolo Cazzaniga ◽  
...  

Abstract Motivation Acute myeloid leukemia (AML) is one of the most common hematological malignancies, characterized by high relapse and mortality rates. The inherent intra-tumor heterogeneity in AML is thought to play an important role in disease recurrence and resistance to chemotherapy. Although experimental protocols for cell proliferation studies are well established and widespread, they are not easily applicable to in vivo contexts, and the analysis of related time-series data is often complex to achieve. To overcome these limitations, model-driven approaches can be exploited to investigate different aspects of cell population dynamics. Results In this work, we present ProCell, a novel modeling and simulation framework to investigate cell proliferation dynamics that, differently from other approaches, takes into account the inherent stochasticity of cell division events. We apply ProCell to compare different models of cell proliferation in AML, notably leveraging experimental data derived from human xenografts in mice. ProCell is coupled with Fuzzy Self-Tuning Particle Swarm Optimization, a swarm-intelligence settings-free algorithm used to automatically infer the models parameterizations. Our results provide new insights on the intricate organization of AML cells with highly heterogeneous proliferative potential, highlighting the important role played by quiescent cells and proliferating cells characterized by different rates of division in the progression and evolution of the disease, thus hinting at the necessity to further characterize tumor cell subpopulations. Availability and implementation The source code of ProCell and the experimental data used in this work are available under the GPL 2.0 license on GITHUB at the following URL: https://github.com/aresio/ProCell. Supplementary information Supplementary data are available at Bioinformatics online.


Entropy ◽  
2019 ◽  
Vol 22 (1) ◽  
pp. 13
Author(s):  
Ivan Anashkin ◽  
Sergey Dyakonov ◽  
German Dyakonov

An expression is proposed that relates the transport properties of polar substances (diffusion coefficient, viscosity coefficient, and thermal conductivity coefficient) with entropy. To calculate the entropy, an equation of state with a good description of the properties in a wide region of the state is used. Comparison of calculations based on the proposed expressions with experimental data showed good agreement. A deviation exceeding 20% is observed only in the region near the critical point as well as at high pressures.


2019 ◽  
Author(s):  
Laura Avino Esteban ◽  
Lyubov R Lonishin ◽  
Daniil Bobrovskiy ◽  
Gregory Leleytner ◽  
Natalya S Bogatyreva ◽  
...  

Abstract Motivation Epistasis, the context-dependence of the contribution of an amino acid substitution to fitness, is common in evolution. To detect epistasis, fitness must be measured for at least four genotypes: the reference genotype, two different single mutants and a double mutant with both of the single mutations. For higher-order epistasis of the order n, fitness has to be measured for all 2n genotypes of an n-dimensional hypercube in genotype space forming a “combinatorially complete dataset”. So far, only a handful of such datasets have been produced by manual curation. Concurrently, random mutagenesis experiments have produced measurements of fitness and other phenotypes in a high-throughput manner, potentially containing a number of combinatorially complete datasets. Results We present an effective recursive algorithm for finding all hypercube structures in random mutagenesis experimental data. To test the algorithm, we applied it to the data from a recent HIS3 protein dataset and found all 199,847,053 unique combinatorially complete genotype combinations of dimensionality ranging from two to twelve. The algorithm may be useful for researchers looking for higher-order epistasis in their high-throughput experimental data. Availability https://github.com/ivankovlab/HypercubeME.git Supplementary information Supplementary data are available at Bioinformatics online.


Sign in / Sign up

Export Citation Format

Share Document