1,283 research outputs found
Fast stereoscopic images with ray-traced volume rendering
Journal ArticleOne of the drawbacks of standard volume rendering techniques is that it is often difficult to comprehend the three-dimensional structure of the volume from a single frame; this is especially true in cases where there is no solid surface. Generally, several frames must be generated and viewed sequentially, using motion parallax to relay depth. Another option is to generate a single stereoscopic pair, resulting in clear and unambiguous depth information in both static and moving images. Methods have been developed which take advantage of the coherence between the two halves of a stereo pair for polygon rendering and ray-tracing, generating the second half of the pair in significantly less time than that required to completely render a single image. This paper reports the results of implementing these techniques with parallel ray-traced volume rendering. In tests with different data types, the time savings is in the range of 70 - 80%
bíogo/hts: high throughput sequence handling for the Go language
biogo/hts provides a Go native implementation of the SAM specification (Group 2016) for SAM and BAM alignment formats (H. et al. 2012) commonly used for representation of high throughput genomic data, the BAI, CSI and tabix indexing formats, and the BGZF blocked compression format. The biogo/hts packages perform parallelized read and write operations and are able to cache recent reads according to user-specified caching methods. The parallelisation approach used by the biogo/hts package is influenced by the approach of the D implementation, sambamba by Tarazov et al. (T. A. et al. 2015). The biogo/hts APIs have been constructed to provide a consistent interface to sequence alignment data and the underlying compression system in order to aid ease of use and tool development.R. Daniel Kortschak, Brent S. Pedersen, and David L. Adelso
A novel hypothesis-unbiased method for gene ontology enrichment based on transcriptome data
Gene Ontology (GO) classification of statistically significantly differentially expressed genes is commonly used to interpret transcriptomics data as a part of functional genomic analysis. In this approach, all significantly expressed genes contribute equally to the final GO classification regardless of their actual expression levels. Gene expression levels can significantly affect protein production and hence should be reflected in GO term enrichment. Genes with low expression levels can also participate in GO term enrichment through cumulative effects. In this report, we have introduced a new GO enrichment method that is suitable for multiple samples and time series experiments that uses a statistical outlier test to detect GO categories with special patterns of variation that can potentially identify candidate biological mechanisms. To demonstrate the value of our approach, we have performed two case studies. Whole transcriptome expression profiles of Salmonella enteritidis and Alzheimer's disease (AD) were analysed in order to determine GO term enrichment across the entire transcriptome instead of a subset of differentially expressed genes used in traditional GO analysis. Our result highlights the key role of inflammation related functional groups in AD pathology as granulocyte colony-stimulating factor receptor binding, neuromedin U binding, and interleukin were remarkably upregulated in AD brain when all using all of the gene expression data in the transcriptome. Mitochondrial components and the molybdopterin synthase complex were identified as potential key cellular components involved in AD pathology.Mario Fruzangohar, Esmaeil Ebrahimie, David L. Adelso
Personalized medicine support system : resolving conflict in allocation to risk groups and predicting patient molecular response to targeted therapy
Treatment management in cancer patients is largely based on the use of a standardized set of predictive and prognostic factors. The former are used to evaluate specific clinical interventions, and they can be useful for selecting treatments because they directly predict the response to a treatment. The latter are used to evaluate a patient’s overall outcomes, and can be used to identify the risks or recurrence of a disease. Current intelligent systems can be a solution for transferring advancements in molecular biology into practice, especially for predicting the molecular response to molecular targeted therapy and the prognosis of risk groups in cancer medicine. This framework primarily focuses on the importance of integrating domain knowledge in predictive and prognostic models for personalized treatment. Our personalized medicine support system provides the needed support in complex decisions and can be incorporated into a treatment guide for selecting molecular targeted therapies.Haneen Banjar, David Adelson, Fred Brown, and Tamara Leclerc
Intelligent techniques using molecular data analysis in leukaemia: an opportunity for personalized medicine support system
The use of intelligent techniques in medicine has brought a ray of hope in terms of treating leukaemia patients. Personalized treatment uses patient’s genetic profile to select a mode of treatment. This process makes use of molecular technology and machine learning, to determine the most suitable approach to treating a leukaemia patient. Until now, no reviews have been published from a computational perspective concerning the development of personalized medicine intelligent techniques for leukaemia patients using molecular data analysis. This review studies the published empirical research on personalized medicine in leukaemia and synthesizes findings across studies related to intelligence techniques in leukaemia, with specific attention to particular categories of these studies to help identify opportunities for further research into personalized medicine support systems in chronic myeloid leukaemia. A systematic search was carried out to identify studies using intelligence techniques in leukaemia and to categorize these studies based on leukaemia type and also the task, data source, and purpose of the studies. Most studies used molecular data analysis for personalized medicine, but future advancement for leukaemia patients requires molecular models that use advanced machine-learning methods to automate decision-making in treatment management to deliver supportive medical information to the patient in clinical practice.Haneen Banjar, David Adelson, Fred Brown, and Naeem Chaudhr
Depth Estimation Through a Generative Model of Light Field Synthesis
Light field photography captures rich structural information that may
facilitate a number of traditional image processing and computer vision tasks.
A crucial ingredient in such endeavors is accurate depth recovery. We present a
novel framework that allows the recovery of a high quality continuous depth map
from light field data. To this end we propose a generative model of a light
field that is fully parametrized by its corresponding depth map. The model
allows for the integration of powerful regularization techniques such as a
non-local means prior, facilitating accurate depth map estimation.Comment: German Conference on Pattern Recognition (GCPR) 201
Associations between perceived teaching behaviors and affect in upper elementary school students.
We explored the associations between student-perceived teaching behaviors and negative affect (NA) and positive affect (PA) in upper elementary age students, both before and after controlling for perceived parenting behaviors. The Teaching Behavior Questionnaire (TBQ), the Alabama Parenting Questionnaire (APQ), and the Positive and Negative Affect Schedule for Children (PANAS-C) were completed by 777 third to fifth graders in nine elementary schools. Using two-level hierarchical linear model analyses, we found that (a) perceived instructional teaching behavior was negatively associated with NA and positively associated with PA; (b) perceived organizational behavior was not associated with either; (c) perceived socio-emotional teaching behavior was positively associated with both; (d) perceived negative teaching behavior was positively associated with NA but not associated with PA. When parenting behaviors were controlled for, the associations with NA but not with PA held up. We discuss implications of the findings for education and mental health personnel
Dichotomy in the Dynamical Status of Massive Cores in Orion
To study the evolution of high mass cores, we have searched for evidence of
collapse motions in a large sample of starless cores in the Orion molecular
cloud. We used the Caltech Submillimeter Observatory telescope to obtain
spectra of the optically thin (\H13CO+) and optically thick (\HCO+) high
density tracer molecules in 27 cores with masses 1 \Ms. The red- and
blue-asymmetries seen in the line profiles of the optically thick line with
respect to the optically thin line indicate that 2/3 of these cores are not
static. We detect evidence for infall (inward motions) in 9 cores and outward
motions for 10 cores, suggesting a dichotomy in the kinematic state of the
non-static cores in this sample. Our results provide an important observational
constraint on the fraction of collapsing (inward motions) versus non-collapsing
(re-expanding) cores for comparison with model simulations.Comment: 9 pages, 2 Figures. To appear in ApJ(Letters
Evolutionary conservation and functional roles of ncRNA
Extent: 11 p.Non-coding RNAs(ncRNAs)are a class of transcribed RNA molecules without protein-coding potential. They were regarded as transcriptional noise,or the by product of genetic information flow from DNA to protein for a long time. However, in recent years, a number of studies have shown that ncRNAs are pervasively transcribed, and most of them show evidence of evolutionary conservation, although less conserved than protein-coding genes. More importantly, many ncRNAs have been confirmed as playing crucial regulatory roles in diverse biological processes and tumorigenesis. Here we summarize the functional significance of this class of “darkmatter” in terms its genomic organization,evolutionary conservation, and broad functional classes.Zhipeng Qu and David L. Adelso
Bovine ncRNAs are abundant, primarily intergenic, conserved and associated with regulatory genes
It is apparent that non-coding transcripts are a common feature of higher organisms and encode uncharacterized layers of genetic regulation and information. We used public bovine EST data from many developmental stages and tissues, and developed a pipeline for the genome wide identification and annotation of non-coding RNAs (ncRNAs). We have predicted 23,060 bovine ncRNAs, 99% of which are un-annotated, based on known ncRNA databases. Intergenic transcripts accounted for the majority (57%) of the predicted ncRNAs and the occurrence of ncRNAs and genes were only moderately correlated (r = 0.55, p-value<2.2e-16). Many of these intergenic non-coding RNAs mapped close to the 3’ or 5’ end of thousands of genes and many of these were transcribed from the opposite strand with respect to the closest gene, particularly regulatory-related genes. Conservation analyses showed that these ncRNAs were evolutionarily conserved, and many intergenic ncRNAs proximate to genes contained sequence-specific motifs. Correlation analysis of expression between these intergenic ncRNAs and protein-coding genes using RNA-seq data from a variety of tissues showed significant correlations with many transcripts. These results support the hypothesis that ncRNAs are common, transcribed in a regulated fashion and have regulatory functions.Zhipeng Qu and David L. Adelso
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