27,674 research outputs found
An Efficient Approach for Polyps Detection in Endoscopic Videos Based on Faster R-CNN
Polyp has long been considered as one of the major etiologies to colorectal
cancer which is a fatal disease around the world, thus early detection and
recognition of polyps plays a crucial role in clinical routines. Accurate
diagnoses of polyps through endoscopes operated by physicians becomes a
challenging task not only due to the varying expertise of physicians, but also
the inherent nature of endoscopic inspections. To facilitate this process,
computer-aid techniques that emphasize fully-conventional image processing and
novel machine learning enhanced approaches have been dedicatedly designed for
polyp detection in endoscopic videos or images. Among all proposed algorithms,
deep learning based methods take the lead in terms of multiple metrics in
evolutions for algorithmic performance. In this work, a highly effective model,
namely the faster region-based convolutional neural network (Faster R-CNN) is
implemented for polyp detection. In comparison with the reported results of the
state-of-the-art approaches on polyps detection, extensive experiments
demonstrate that the Faster R-CNN achieves very competing results, and it is an
efficient approach for clinical practice.Comment: 6 pages, 10 figures,2018 International Conference on Pattern
Recognitio
Sparse integrative clustering of multiple omics data sets
High resolution microarrays and second-generation sequencing platforms are
powerful tools to investigate genome-wide alterations in DNA copy number,
methylation and gene expression associated with a disease. An integrated
genomic profiling approach measures multiple omics data types simultaneously in
the same set of biological samples. Such approach renders an integrated data
resolution that would not be available with any single data type. In this
study, we use penalized latent variable regression methods for joint modeling
of multiple omics data types to identify common latent variables that can be
used to cluster patient samples into biologically and clinically relevant
disease subtypes. We consider lasso [J. Roy. Statist. Soc. Ser. B 58 (1996)
267-288], elastic net [J. R. Stat. Soc. Ser. B Stat. Methodol. 67 (2005)
301-320] and fused lasso [J. R. Stat. Soc. Ser. B Stat. Methodol. 67 (2005)
91-108] methods to induce sparsity in the coefficient vectors, revealing
important genomic features that have significant contributions to the latent
variables. An iterative ridge regression is used to compute the sparse
coefficient vectors. In model selection, a uniform design [Monographs on
Statistics and Applied Probability (1994) Chapman & Hall] is used to seek
"experimental" points that scattered uniformly across the search domain for
efficient sampling of tuning parameter combinations. We compared our method to
sparse singular value decomposition (SVD) and penalized Gaussian mixture model
(GMM) using both real and simulated data sets. The proposed method is applied
to integrate genomic, epigenomic and transcriptomic data for subtype analysis
in breast and lung cancer data sets.Comment: Published in at http://dx.doi.org/10.1214/12-AOAS578 the Annals of
Applied Statistics (http://www.imstat.org/aoas/) by the Institute of
Mathematical Statistics (http://www.imstat.org
The clustering of galaxies with pseudo bulge and classical bulge in the local Universe
We investigate the clustering properties and close neighbour counts for
galaxies with different types of bulges and stellar masses. We select samples
of "classical" and "pseudo" bulges, as well as "bulge-less" disk galaxies,
based on the bulge/disk decomposition catalog of SDSS galaxies provided by
Simard et al. (2011). For a given galaxy sample we estimate: the projected
two-point cross-correlation function with respect to a spectroscopic reference
sample, w_p(r_p), and the average background-subtracted neighbour count within
a projected separation using a photometric reference sample, N_neighbour(<r_p).
We compare the results with the measurements of control samples matched in
color, concentration and redshift. We find that, when limited to a certain
stellar mass range and matched in color and concentration, all the samples
present similar clustering amplitudes and neighbour counts on scales above
~0.1h^{-1}Mpc. This indicates that neither the presence of a central bulge, nor
the bulge type is related to intermediate-to-large scale environments. On
smaller scales, in contrast, pseudo-bulge and pure-disk galaxies similarly show
strong excess in close neighbour count when compared to control galaxies, at
all masses probed. For classical bulges, small-scale excess is also observed
but only for M_stars < 10^{10} M_sun; at higher masses, their neighbour counts
are similar to that of control galaxies at all scales. These results imply
strong connections between galactic bulges and galaxy-galaxy interactions in
the local Universe, although it is unclear how they are physically linked in
the current theory of galaxy formation.Comment: 14 pages, 16 figures, accepted for publication in MNRA
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