Reconfigurable acceleration of genetic sequence alignment: A survey of two decades of efforts

Genetic sequence alignment has always been a computational challenge in bioinformatics. Depending on the problem size, software-based aligners can take multiple CPU-days to process the sequence data, creating a bottleneck point in bioinformatic analysis flow. Reconfigurable accelerator can achieve high performance for such computation by providing massive parallelism, but at the expense of programming flexibility and thus has not been commensurately used by practitioners. Therefore, this paper aims to provide a thorough survey of the proposed accelerators by giving a qualitative categorization based on their algorithms and speedup. A comprehensive comparison between work is also presented so as to guide selection for biologist, and to provide insight on future research direction for FPGA scientists

A study on the effect of stroop test on the formation of students discipline by using the Heart Rate Variability (HRV) technique

Discipline refers to self-control and individual behaviour. Other than that, discipline is an important element in the formation of integrity level. The objective of the study is to assess the effects of using the Stroop test of biofeedback protocol in order to evaluate individual level of discipline. A clinical study has been conducted on 50 participants which is the participants is a undergraduate student from Universiti Malaysia Pahang, who were divided into two groups. First group is students get high achiever and second group is students get low achierver in academic. The Heart Rate Variability (HRV) technique has been used in the assessment of this protocol. The findings show that there was a positive relationship between the Stroop test and the students discipline that those who excelled managed to get higher score of LF spectrum as compared to HF and VLF, while the students with lower achievement showed higher score of VLF and HF spectrum than LF. In conclusion, this test is one of the tests that can be used in increasing the level of individual discipline

FPGA Acceleration of Pre-Alignment Filters for Short Read Mapping With HLS

Pre-alignment filters are useful for reducing the computational requirements of genomic sequence mappers. Most of them are based on estimating or computing the edit distance between sequences and their candidate locations in a reference genome using a subset of the dynamic programming table used to compute Levenshtein distance. Some of their FPGA implementations of use classic HDL toolchains, thus limiting their portability. Currently, most FPGA accelerators offered by heterogeneous cloud providers support C/C++ HLS. In this work, we implement and optimize several state-of-the-art pre-alignment filters using C/C++ based-HLS to expand their portability to a wide range of systems supporting the OpenCL runtime. Moreover, we perform a complete analysis of the performance and accuracy of the filters and analyze the implications of the results. The maximum throughput obtained by an exact filter is 95.1 MPairs/s including memory transfers using 100 bp sequences, which is the highest ever reported for a comparable system and more than two times faster than previous HDL-based results. The best energy efficiency obtained from the accelerator (not considering host CPU) is 2.1 MPairs/J, more than one order of magnitude higher than other accelerator-based comparable approaches from the state of the art.10.13039/501100008530-European Union Regional Development Fund (ERDF) within the framework of the ERDF Operational Program of Catalonia 2014-2020 with a grant of 50% of the total cost eligible under the Designing RISC-V based Accelerators for next generation computers project (DRAC) (Grant Number: [001-P-001723]) 10.13039/501100002809-Catalan Government (Grant Number: 2017-SGR-313 and 2017-SGR-1624) 10.13039/501100004837-Spanish Ministry of Science, Innovation and Universities (Grant Number: PID2020-113614RB-C21 and RTI2018-095209-B-C22)Peer ReviewedPostprint (published version

FPGA acceleration of DNA sequence alignment: design analysis and optimization

Existing FPGA accelerators for short read mapping often fail to utilize the complete biological information in sequencing data for simple hardware design, leading to missed or incorrect alignment. In this work, we propose a runtime reconfigurable alignment pipeline that considers all information in sequencing data for the biologically accurate acceleration of short read mapping. We focus our efforts on accelerating two string matching techniques: FM-index and the Smith-Waterman algorithm with the affine-gap model which are commonly used in short read mapping. We further optimize the FPGA hardware using a design analyzer and merger to improve alignment performance. The contributions of this work are as follows. 1. We accelerate the exact-match and mismatch alignment by leveraging the FM-index technique. We optimize memory access by compressing the data structure and interleaving the access with multiple short reads. The FM-index hardware also considers complete information in the read data to maximize accuracy. 2. We propose a seed-and-extend model to accelerate alignment with indels. The FM-index hardware is extended to support the seeding stage while a Smith-Waterman implementation with the affine-gap model is developed on FPGA for the extension stage. This model can improve the efficiency of indel alignment with comparable accuracy versus state-of-the-art software. 3. We present an approach for merging multiple FPGA designs into a single hardware design, so that multiple place-and-route tasks can be replaced by a single task to speed up functional evaluation of designs. We first experiment with this approach to demonstrate its feasibility for different designs. Then we apply this approach to optimize one of the proposed FPGA aligners for better alignment performance.Open Acces

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