|
Records |
Links |
|
Author |
Meysam Madadi; Sergio Escalera; Jordi Gonzalez; Xavier Roca; Felipe Lumbreras |
![goto web page (via DOI) doi](http://refbase.cvc.uab.es/img/doi.gif)
|
|
Title |
Multi-part body segmentation based on depth maps for soft biometry analysis |
Type |
Journal Article |
|
Year |
2015 |
Publication |
Pattern Recognition Letters |
Abbreviated Journal |
PRL |
|
|
Volume |
56 |
Issue |
|
Pages |
14-21 |
|
|
Keywords |
3D shape context; 3D point cloud alignment; Depth maps; Human body segmentation; Soft biometry analysis |
|
|
Abstract |
This paper presents a novel method extracting biometric measures using depth sensors. Given a multi-part labeled training data, a new subject is aligned to the best model of the dataset, and soft biometrics such as lengths or circumference sizes of limbs and body are computed. The process is performed by training relevant pose clusters, defining a representative model, and fitting a 3D shape context descriptor within an iterative matching procedure. We show robust measures by applying orthogonal plates to body hull. We test our approach in a novel full-body RGB-Depth data set, showing accurate estimation of soft biometrics and better segmentation accuracy in comparison with random forest approach without requiring large training data. |
|
|
Address |
|
|
|
Corporate Author |
|
Thesis |
|
|
|
Publisher ![sorted by Publisher field, ascending order (up)](http://refbase.cvc.uab.es/img/sort_asc.gif) |
|
Place of Publication |
|
Editor |
|
|
|
Language |
|
Summary Language |
|
Original Title |
|
|
|
Series Editor |
|
Series Title |
|
Abbreviated Series Title |
|
|
|
Series Volume |
|
Series Issue |
|
Edition |
|
|
|
ISSN |
|
ISBN |
|
Medium |
|
|
|
Area |
|
Expedition |
|
Conference |
|
|
|
Notes |
HuPBA; ISE; ADAS; 600.076;600.049; 600.063; 600.054; 302.018;MILAB |
Approved |
no |
|
|
Call Number |
Admin @ si @ MEG2015 |
Serial |
2588 |
|
Permanent link to this record |
|
|
|
|
Author |
Frederic Sampedro; Anna Domenech; Sergio Escalera; Ignasi Carrio |
![goto web page (via DOI) doi](http://refbase.cvc.uab.es/img/doi.gif)
|
|
Title |
Deriving global quantitative tumor response parameters from 18F-FDG PET-CT scans in patients with non-Hodgkins lymphoma |
Type |
Journal Article |
|
Year |
2015 |
Publication |
Nuclear Medicine Communications |
Abbreviated Journal |
NMC |
|
|
Volume |
36 |
Issue |
4 |
Pages |
328-333 |
|
|
Keywords |
|
|
|
Abstract |
OBJECTIVES:
The aim of the study was to address the need for quantifying the global cancer time evolution magnitude from a pair of time-consecutive positron emission tomography-computed tomography (PET-CT) scans. In particular, we focus on the computation of indicators using image-processing techniques that seek to model non-Hodgkin's lymphoma (NHL) progression or response severity.
MATERIALS AND METHODS:
A total of 89 pairs of time-consecutive PET-CT scans from NHL patients were stored in a nuclear medicine station for subsequent analysis. These were classified by a consensus of nuclear medicine physicians into progressions, partial responses, mixed responses, complete responses, and relapses. The cases of each group were ordered by magnitude following visual analysis. Thereafter, a set of quantitative indicators designed to model the cancer evolution magnitude within each group were computed using semiautomatic and automatic image-processing techniques. Performance evaluation of the proposed indicators was measured by a correlation analysis with the expert-based visual analysis.
RESULTS:
The set of proposed indicators achieved Pearson's correlation results in each group with respect to the expert-based visual analysis: 80.2% in progressions, 77.1% in partial response, 68.3% in mixed response, 88.5% in complete response, and 100% in relapse. In the progression and mixed response groups, the proposed indicators outperformed the common indicators used in clinical practice [changes in metabolic tumor volume, mean, maximum, peak standardized uptake value (SUV mean, SUV max, SUV peak), and total lesion glycolysis] by more than 40%.
CONCLUSION:
Computing global indicators of NHL response using PET-CT imaging techniques offers a strong correlation with the associated expert-based visual analysis, motivating the future incorporation of such quantitative and highly observer-independent indicators in oncological decision making or treatment response evaluation scenarios. |
|
|
Address |
|
|
|
Corporate Author |
|
Thesis |
|
|
|
Publisher ![sorted by Publisher field, ascending order (up)](http://refbase.cvc.uab.es/img/sort_asc.gif) |
|
Place of Publication |
|
Editor |
|
|
|
Language |
|
Summary Language |
|
Original Title |
|
|
|
Series Editor |
|
Series Title |
|
Abbreviated Series Title |
|
|
|
Series Volume |
|
Series Issue |
|
Edition |
|
|
|
ISSN |
|
ISBN |
|
Medium |
|
|
|
Area |
|
Expedition |
|
Conference |
|
|
|
Notes |
HuPBA;MILAB |
Approved |
no |
|
|
Call Number |
Admin @ si @ SDE2015 |
Serial |
2605 |
|
Permanent link to this record |
|
|
|
|
Author |
Adriana Romero; Petia Radeva; Carlo Gatta |
![goto web page (via DOI) doi](http://refbase.cvc.uab.es/img/doi.gif)
|
|
Title |
Meta-parameter free unsupervised sparse feature learning |
Type |
Journal Article |
|
Year |
2015 |
Publication |
IEEE Transactions on Pattern Analysis and Machine Intelligence |
Abbreviated Journal |
TPAMI |
|
|
Volume |
37 |
Issue |
8 |
Pages |
1716-1722 |
|
|
Keywords |
|
|
|
Abstract |
We propose a meta-parameter free, off-the-shelf, simple and fast unsupervised feature learning algorithm, which exploits a new way of optimizing for sparsity. Experiments on CIFAR-10, STL- 10 and UCMerced show that the method achieves the state-of-theart performance, providing discriminative features that generalize well. |
|
|
Address |
|
|
|
Corporate Author |
|
Thesis |
|
|
|
Publisher ![sorted by Publisher field, ascending order (up)](http://refbase.cvc.uab.es/img/sort_asc.gif) |
|
Place of Publication |
|
Editor |
|
|
|
Language |
|
Summary Language |
|
Original Title |
|
|
|
Series Editor |
|
Series Title |
|
Abbreviated Series Title |
|
|
|
Series Volume |
|
Series Issue |
|
Edition |
|
|
|
ISSN |
|
ISBN |
|
Medium |
|
|
|
Area |
|
Expedition |
|
Conference |
|
|
|
Notes |
MILAB; 600.068; 600.079; 601.160 |
Approved |
no |
|
|
Call Number |
Admin @ si @ RRG2014b |
Serial |
2594 |
|
Permanent link to this record |
|
|
|
|
Author |
Frederic Sampedro; Sergio Escalera; Anna Domenech; Ignasi Carrio |
![goto web page (via DOI) doi](http://refbase.cvc.uab.es/img/doi.gif)
|
|
Title |
A computational framework for cancer response assessment based on oncological PET-CT scans |
Type |
Journal Article |
|
Year |
2014 |
Publication |
Computers in Biology and Medicine |
Abbreviated Journal |
CBM |
|
|
Volume |
55 |
Issue |
|
Pages |
92–99 |
|
|
Keywords |
Computer aided diagnosis; Nuclear medicine; Machine learning; Image processing; Quantitative analysis |
|
|
Abstract |
In this work we present a comprehensive computational framework to help in the clinical assessment of cancer response from a pair of time consecutive oncological PET-CT scans. In this scenario, the design and implementation of a supervised machine learning system to predict and quantify cancer progression or response conditions by introducing a novel feature set that models the underlying clinical context is described. Performance results in 100 clinical cases (corresponding to 200 whole body PET-CT scans) in comparing expert-based visual analysis and classifier decision making show up to 70% accuracy within a completely automatic pipeline and 90% accuracy when providing the system with expert-guided PET tumor segmentation masks. |
|
|
Address |
|
|
|
Corporate Author |
|
Thesis |
|
|
|
Publisher ![sorted by Publisher field, ascending order (up)](http://refbase.cvc.uab.es/img/sort_asc.gif) |
|
Place of Publication |
|
Editor |
|
|
|
Language |
|
Summary Language |
|
Original Title |
|
|
|
Series Editor |
|
Series Title |
|
Abbreviated Series Title |
|
|
|
Series Volume |
|
Series Issue |
|
Edition |
|
|
|
ISSN |
|
ISBN |
|
Medium |
|
|
|
Area |
|
Expedition |
|
Conference |
|
|
|
Notes |
HuPBA;MILAB |
Approved |
no |
|
|
Call Number |
Admin @ si @ SED2014 |
Serial |
2606 |
|
Permanent link to this record |
|
|
|
|
Author |
Mariella Dimiccoli |
![download PDF file pdf](http://refbase.cvc.uab.es/img/file_PDF.gif)
![find record details (via OpenURL) openurl](http://refbase.cvc.uab.es/img/xref.gif)
|
|
Title |
Figure-ground segregation: A fully nonlocal approach |
Type |
Journal Article |
|
Year |
2016 |
Publication |
Vision Research |
Abbreviated Journal |
VR |
|
|
Volume |
126 |
Issue |
|
Pages |
308-317 |
|
|
Keywords |
Figure-ground segregation; Nonlocal approach; Directional linear voting; Nonlinear diffusion |
|
|
Abstract |
We present a computational model that computes and integrates in a nonlocal fashion several configural cues for automatic figure-ground segregation. Our working hypothesis is that the figural status of each pixel is a nonlocal function of several geometric shape properties and it can be estimated without explicitly relying on object boundaries. The methodology is grounded on two elements: multi-directional linear voting and nonlinear diffusion. A first estimation of the figural status of each pixel is obtained as a result of a voting process, in which several differently oriented line-shaped neighborhoods vote to express their belief about the figural status of the pixel. A nonlinear diffusion process is then applied to enforce the coherence of figural status estimates among perceptually homogeneous regions. Computer simulations fit human perception and match the experimental evidence that several cues cooperate in defining figure-ground segregation. The results of this work suggest that figure-ground segregation involves feedback from cells with larger receptive fields in higher visual cortical areas. |
|
|
Address |
|
|
|
Corporate Author |
|
Thesis |
|
|
|
Publisher ![sorted by Publisher field, ascending order (up)](http://refbase.cvc.uab.es/img/sort_asc.gif) |
|
Place of Publication |
|
Editor |
|
|
|
Language |
|
Summary Language |
|
Original Title |
|
|
|
Series Editor |
|
Series Title |
|
Abbreviated Series Title |
|
|
|
Series Volume |
|
Series Issue |
|
Edition |
|
|
|
ISSN |
|
ISBN |
|
Medium |
|
|
|
Area |
|
Expedition |
|
Conference |
|
|
|
Notes |
MILAB; |
Approved |
no |
|
|
Call Number |
Admin @ si @ Dim2016b |
Serial |
2623 |
|
Permanent link to this record |