141,253 research outputs found
Feature and viewpoint selection for industrial car assembly
Abstract. Quality assurance programs of today’s car manufacturers show increasing demand for automated visual inspection tasks. A typical example is just-in-time checking of assemblies along production lines. Since high throughput must be achieved, object recognition and pose estimation heavily rely on offline preprocessing stages of available CAD data. In this paper, we propose a complete, universal framework for CAD model feature extraction and entropy index based viewpoint selection that is developed in cooperation with a major german car manufacturer
Topic Independent Identification of Agreement and Disagreement in Social Media Dialogue
Research on the structure of dialogue has been hampered for years because
large dialogue corpora have not been available. This has impacted the dialogue
research community's ability to develop better theories, as well as good off
the shelf tools for dialogue processing. Happily, an increasing amount of
information and opinion exchange occur in natural dialogue in online forums,
where people share their opinions about a vast range of topics. In particular
we are interested in rejection in dialogue, also called disagreement and
denial, where the size of available dialogue corpora, for the first time,
offers an opportunity to empirically test theoretical accounts of the
expression and inference of rejection in dialogue. In this paper, we test
whether topic-independent features motivated by theoretical predictions can be
used to recognize rejection in online forums in a topic independent way. Our
results show that our theoretically motivated features achieve 66% accuracy, an
improvement over a unigram baseline of an absolute 6%.Comment: @inproceedings{Misra2013TopicII, title={Topic Independent
Identification of Agreement and Disagreement in Social Media Dialogue},
author={Amita Misra and Marilyn A. Walker}, booktitle={SIGDIAL Conference},
year={2013}
An Efficient Primal-Dual Prox Method for Non-Smooth Optimization
We study the non-smooth optimization problems in machine learning, where both
the loss function and the regularizer are non-smooth functions. Previous
studies on efficient empirical loss minimization assume either a smooth loss
function or a strongly convex regularizer, making them unsuitable for
non-smooth optimization. We develop a simple yet efficient method for a family
of non-smooth optimization problems where the dual form of the loss function is
bilinear in primal and dual variables. We cast a non-smooth optimization
problem into a minimax optimization problem, and develop a primal dual prox
method that solves the minimax optimization problem at a rate of
{assuming that the proximal step can be efficiently solved}, significantly
faster than a standard subgradient descent method that has an
convergence rate. Our empirical study verifies the efficiency of the proposed
method for various non-smooth optimization problems that arise ubiquitously in
machine learning by comparing it to the state-of-the-art first order methods
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GenEpi: gene-based epistasis discovery using machine learning.
BackgroundGenome-wide association studies (GWAS) provide a powerful means to identify associations between genetic variants and phenotypes. However, GWAS techniques for detecting epistasis, the interactions between genetic variants associated with phenotypes, are still limited. We believe that developing an efficient and effective GWAS method to detect epistasis will be a key for discovering sophisticated pathogenesis, which is especially important for complex diseases such as Alzheimer's disease (AD).ResultsIn this regard, this study presents GenEpi, a computational package to uncover epistasis associated with phenotypes by the proposed machine learning approach. GenEpi identifies both within-gene and cross-gene epistasis through a two-stage modeling workflow. In both stages, GenEpi adopts two-element combinatorial encoding when producing features and constructs the prediction models by L1-regularized regression with stability selection. The simulated data showed that GenEpi outperforms other widely-used methods on detecting the ground-truth epistasis. As real data is concerned, this study uses AD as an example to reveal the capability of GenEpi in finding disease-related variants and variant interactions that show both biological meanings and predictive power.ConclusionsThe results on simulation data and AD demonstrated that GenEpi has the ability to detect the epistasis associated with phenotypes effectively and efficiently. The released package can be generalized to largely facilitate the studies of many complex diseases in the near future
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