23,482 research outputs found
The Parallelism Motifs of Genomic Data Analysis
Genomic data sets are growing dramatically as the cost of sequencing
continues to decline and small sequencing devices become available. Enormous
community databases store and share this data with the research community, but
some of these genomic data analysis problems require large scale computational
platforms to meet both the memory and computational requirements. These
applications differ from scientific simulations that dominate the workload on
high end parallel systems today and place different requirements on programming
support, software libraries, and parallel architectural design. For example,
they involve irregular communication patterns such as asynchronous updates to
shared data structures. We consider several problems in high performance
genomics analysis, including alignment, profiling, clustering, and assembly for
both single genomes and metagenomes. We identify some of the common
computational patterns or motifs that help inform parallelization strategies
and compare our motifs to some of the established lists, arguing that at least
two key patterns, sorting and hashing, are missing
Next-generation sequencing: applications beyond genomes.
The development of DNA sequencing more than 30 years ago has profoundly impacted biological research. In the last couple of years, remarkable technological innovations have emerged that allow the direct and cost-effective sequencing of complex samples at unprecedented scale and speed. These next-generation technologies make it feasible to sequence not only static genomes, but also entire transcriptomes expressed under different conditions. These and other powerful applications of next-generation sequencing are rapidly revolutionizing the way genomic studies are carried out. Below, we provide a snapshot of these exciting new approaches to understanding the properties and functions of genomes. Given that sequencing-based assays may increasingly supersede microarray-based assays, we also compare and contrast data obtained from these distinct approaches
Applications and Challenges of Real-time Mobile DNA Analysis
The DNA sequencing is the process of identifying the exact order of
nucleotides within a given DNA molecule. The new portable and relatively
inexpensive DNA sequencers, such as Oxford Nanopore MinION, have the potential
to move DNA sequencing outside of laboratory, leading to faster and more
accessible DNA-based diagnostics. However, portable DNA sequencing and analysis
are challenging for mobile systems, owing to high data throughputs and
computationally intensive processing performed in environments with unreliable
connectivity and power.
In this paper, we provide an analysis of the challenges that mobile systems
and mobile computing must address to maximize the potential of portable DNA
sequencing, and in situ DNA analysis. We explain the DNA sequencing process and
highlight the main differences between traditional and portable DNA sequencing
in the context of the actual and envisioned applications. We look at the
identified challenges from the perspective of both algorithms and systems
design, showing the need for careful co-design
A network approach for managing and processing big cancer data in clouds
Translational cancer research requires integrative analysis of multiple levels of big cancer data to identify and treat cancer. In order to address the issues that data is decentralised, growing and continually being updated, and the content living or archiving on different information sources partially overlaps creating redundancies as well as contradictions and inconsistencies, we develop a data network model and technology for constructing and managing big cancer data. To support our data network approach for data process and analysis, we employ a semantic content network approach and adopt the CELAR cloud platform. The prototype implementation shows that the CELAR cloud can satisfy the on-demanding needs of various data resources for management and process of big cancer data
DeepConv-DTI: Prediction of drug-target interactions via deep learning with convolution on protein sequences
Identification of drug-target interactions (DTIs) plays a key role in drug
discovery. The high cost and labor-intensive nature of in vitro and in vivo
experiments have highlighted the importance of in silico-based DTI prediction
approaches. In several computational models, conventional protein descriptors
are shown to be not informative enough to predict accurate DTIs. Thus, in this
study, we employ a convolutional neural network (CNN) on raw protein sequences
to capture local residue patterns participating in DTIs. With CNN on protein
sequences, our model performs better than previous protein descriptor-based
models. In addition, our model performs better than the previous deep learning
model for massive prediction of DTIs. By examining the pooled convolution
results, we found that our model can detect binding sites of proteins for DTIs.
In conclusion, our prediction model for detecting local residue patterns of
target proteins successfully enriches the protein features of a raw protein
sequence, yielding better prediction results than previous approaches.Comment: 26 pages, 7 figure
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