The solution structure of homotrimetallic lanthanide helicates investigated with novel model-free multi-centre paramagnetic NMR methodsElectronic supplementary information (ESI) available: tables of structural factors Cikl, Dikl obtained for the model complexes and for [Ln3(L1)3]9+ in solution (Table S1) and geometrical factors calculated for the structure of [Eu3(L1)3]9+ optimized in the gas phase (Table S2). Figures showing a plot of 1/Tpara1i vs. according to eqn. (19) (Fig. S1), a plot of AFikl for the 165 Hikl triplets in [Ln3(L1)3]9+ (Fig. S2) and comparisons of structural parameters between the optimized gas phase model and the solution structure (Figs. S3 and S4). See http://www.rsc.org/suppdata/dt/b2/b212352e/

2003 ◽  
pp. 1251-1263 ◽  
Author(s):  
Nadjet Ouali ◽  
Jean-Pierre Rivera ◽  
Pierre-Yves Morgantini ◽  
Jacques Weber ◽  
Claude Piguet
2007 ◽  
Vol 26 (8) ◽  
pp. 2070-2076 ◽  
Author(s):  
Brandon S. Tackett ◽  
Chandana Karunatilaka ◽  
Adam M. Daly ◽  
Stephen G. Kukolich

2021 ◽  
Vol 6 (42) ◽  
pp. 11779-11787
Author(s):  
Yunping Zhai ◽  
Youju Wang ◽  
Junwen Chen ◽  
Shihang Liang ◽  
Yongrui Wang ◽  
...  

2019 ◽  
Vol 123 (28) ◽  
pp. 5995-6002 ◽  
Author(s):  
Kamal K. Mishra ◽  
Santosh K. Singh ◽  
Satish Kumar ◽  
Gulzar Singh ◽  
Biplab Sarkar ◽  
...  

2019 ◽  
Vol 35 (14) ◽  
pp. i427-i435 ◽  
Author(s):  
Héctor Climente-González ◽  
Chloé-Agathe Azencott ◽  
Samuel Kaski ◽  
Makoto Yamada

AbstractMotivationFinding non-linear relationships between biomolecules and a biological outcome is computationally expensive and statistically challenging. Existing methods have important drawbacks, including among others lack of parsimony, non-convexity and computational overhead. Here we propose block HSIC Lasso, a non-linear feature selector that does not present the previous drawbacks.ResultsWe compare block HSIC Lasso to other state-of-the-art feature selection techniques in both synthetic and real data, including experiments over three common types of genomic data: gene-expression microarrays, single-cell RNA sequencing and genome-wide association studies. In all cases, we observe that features selected by block HSIC Lasso retain more information about the underlying biology than those selected by other techniques. As a proof of concept, we applied block HSIC Lasso to a single-cell RNA sequencing experiment on mouse hippocampus. We discovered that many genes linked in the past to brain development and function are involved in the biological differences between the types of neurons.Availability and implementationBlock HSIC Lasso is implemented in the Python 2/3 package pyHSICLasso, available on PyPI. Source code is available on GitHub (https://github.com/riken-aip/pyHSICLasso).Supplementary informationSupplementary data are available at Bioinformatics online.


Author(s):  
Tao Jiang ◽  
Yuanyuan Li ◽  
Alison A Motsinger-Reif

Abstract Motivation The recently proposed knockoff filter is a general framework for controlling the false discovery rate (FDR) when performing variable selection. This powerful new approach generates a ‘knockoff’ of each variable tested for exact FDR control. Imitation variables that mimic the correlation structure found within the original variables serve as negative controls for statistical inference. Current applications of knockoff methods use linear regression models and conduct variable selection only for variables existing in model functions. Here, we extend the use of knockoffs for machine learning with boosted trees, which are successful and widely used in problems where no prior knowledge of model function is required. However, currently available importance scores in tree models are insufficient for variable selection with FDR control. Results We propose a novel strategy for conducting variable selection without prior model topology knowledge using the knockoff method with boosted tree models. We extend the current knockoff method to model-free variable selection through the use of tree-based models. Additionally, we propose and evaluate two new sampling methods for generating knockoffs, namely the sparse covariance and principal component knockoff methods. We test and compare these methods with the original knockoff method regarding their ability to control type I errors and power. In simulation tests, we compare the properties and performance of importance test statistics of tree models. The results include different combinations of knockoffs and importance test statistics. We consider scenarios that include main-effect, interaction, exponential and second-order models while assuming the true model structures are unknown. We apply our algorithm for tumor purity estimation and tumor classification using Cancer Genome Atlas (TCGA) gene expression data. Our results show improved discrimination between difficult-to-discriminate cancer types. Availability and implementation The proposed algorithm is included in the KOBT package, which is available at https://cran.r-project.org/web/packages/KOBT/index.html. Supplementary information Supplementary data are available at Bioinformatics online.


Author(s):  
Xiaofan Lu ◽  
Jialin Meng ◽  
Yujie Zhou ◽  
Liyun Jiang ◽  
Fangrong Yan

Abstract Summary Stratification of cancer patients into distinct molecular subgroups based on multi-omics data is an important issue in the context of precision medicine. Here, we present MOVICS, an R package for multi-omics integration and visualization in cancer subtyping. MOVICS provides a unified interface for 10 state-of-the-art multi-omics integrative clustering algorithms, and incorporates the most commonly used downstream analyses in cancer subtyping researches, including characterization and comparison of identified subtypes from multiple perspectives, and verification of subtypes in external cohort using two model-free approaches for multiclass prediction. MOVICS also creates feature rich customizable visualizations with minimal effort. By analysing two published breast cancer cohort, we signifies that MOVICS can serve a wide range of users and assist cancer therapy by moving away from the ‘one-size-fits-all’ approach to patient care. Availability and implementation MOVICS package and online tutorial are freely available at https://github.com/xlucpu/MOVICS. Supplementary information Supplementary data are available at Bioinformatics online.


2013 ◽  
Vol 712-715 ◽  
pp. 2035-2038
Author(s):  
Hua Yi Tang ◽  
Shu Li Pan ◽  
Ping Jie Huang ◽  
Di Bo Hou ◽  
Guang Xin Zhang

Eddy current testing technique has been widely used in a variety of fields, many researches have been done in quantitative estimation in conductive structure. In the actual use of ECT system, lift-off effect is an inevitable factor which is still a challenging task. Hence, the objectives of this study are to introduce a novel model-free method Support Vector Regression optimized by Particle Swarm Optimization (PSO-SVR) to estimate the surface defect with variable lift-off. Experimental validation carried out that the proposed method had a good performance in surface defect estimation with lift-off effect.


Sign in / Sign up

Export Citation Format

Share Document