73,820 research outputs found

    BioWorkbench: A High-Performance Framework for Managing and Analyzing Bioinformatics Experiments

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    Advances in sequencing techniques have led to exponential growth in biological data, demanding the development of large-scale bioinformatics experiments. Because these experiments are computation- and data-intensive, they require high-performance computing (HPC) techniques and can benefit from specialized technologies such as Scientific Workflow Management Systems (SWfMS) and databases. In this work, we present BioWorkbench, a framework for managing and analyzing bioinformatics experiments. This framework automatically collects provenance data, including both performance data from workflow execution and data from the scientific domain of the workflow application. Provenance data can be analyzed through a web application that abstracts a set of queries to the provenance database, simplifying access to provenance information. We evaluate BioWorkbench using three case studies: SwiftPhylo, a phylogenetic tree assembly workflow; SwiftGECKO, a comparative genomics workflow; and RASflow, a RASopathy analysis workflow. We analyze each workflow from both computational and scientific domain perspectives, by using queries to a provenance and annotation database. Some of these queries are available as a pre-built feature of the BioWorkbench web application. Through the provenance data, we show that the framework is scalable and achieves high-performance, reducing up to 98% of the case studies execution time. We also show how the application of machine learning techniques can enrich the analysis process

    A perceptual hash function to store and retrieve large scale DNA sequences

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    This paper proposes a novel approach for storing and retrieving massive DNA sequences.. The method is based on a perceptual hash function, commonly used to determine the similarity between digital images, that we adapted for DNA sequences. Perceptual hash function presented here is based on a Discrete Cosine Transform Sign Only (DCT-SO). Each nucleotide is encoded as a fixed gray level intensity pixel and the hash is calculated from its significant frequency characteristics. This results to a drastic data reduction between the sequence and the perceptual hash. Unlike cryptographic hash functions, perceptual hashes are not affected by "avalanche effect" and thus can be compared. The similarity distance between two hashes is estimated with the Hamming Distance, which is used to retrieve DNA sequences. Experiments that we conducted show that our approach is relevant for storing massive DNA sequences, and retrieving them

    A highly parameterized and efficient FPGA-based skeleton for pairwise biological sequence alignment

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    Automatic Translating Between Ancient Chinese and Contemporary Chinese with Limited Aligned Corpora

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    The Chinese language has evolved a lot during the long-term development. Therefore, native speakers now have trouble in reading sentences written in ancient Chinese. In this paper, we propose to build an end-to-end neural model to automatically translate between ancient and contemporary Chinese. However, the existing ancient-contemporary Chinese parallel corpora are not aligned at the sentence level and sentence-aligned corpora are limited, which makes it difficult to train the model. To build the sentence level parallel training data for the model, we propose an unsupervised algorithm that constructs sentence-aligned ancient-contemporary pairs by using the fact that the aligned sentence pair shares many of the tokens. Based on the aligned corpus, we propose an end-to-end neural model with copying mechanism and local attention to translate between ancient and contemporary Chinese. Experiments show that the proposed unsupervised algorithm achieves 99.4% F1 score for sentence alignment, and the translation model achieves 26.95 BLEU from ancient to contemporary, and 36.34 BLEU from contemporary to ancient.Comment: Acceptted by NLPCC 201

    The Parallelism Motifs of Genomic Data Analysis

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    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
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