2008 International Conference on Reconfigurable Computing and FPGAs 2008
DOI: 10.1109/reconfig.2008.30
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Sequence Alignment with Traceback on Reconfigurable Hardware

Abstract: Biological sequence alignment is an essential tool used in molecular biology and biomedical applications. The growing volume of genetic data and the complexity of sequence alignment present a challenge in obtaining alignment results in a timely manner. Known methods to accelerate alignment on reconfigurable hardware only address sequence comparison, limit the sequence length, or exhibit memory and I/O bottlenecks. A space-efficient, global sequence alignment algorithm and architecture is presented that acceler… Show more

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Cited by 10 publications
(13 citation statements)
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“…We get the following conclusions: (1) compared to hardware SW alignment with backtracking [12,14,20], our implementation is able to implement larger PE array and obtains higher frequency and performance. (2) Compared to other hardware SW implementations without backtracking, our comprehensive computing performance is also superior to others obviously.…”
Section: Performance Comparison With Fpga Platformsmentioning
confidence: 75%
See 2 more Smart Citations
“…We get the following conclusions: (1) compared to hardware SW alignment with backtracking [12,14,20], our implementation is able to implement larger PE array and obtains higher frequency and performance. (2) Compared to other hardware SW implementations without backtracking, our comprehensive computing performance is also superior to others obviously.…”
Section: Performance Comparison With Fpga Platformsmentioning
confidence: 75%
“…Most GPU-based SW implementations [28,29,37] adopt intra-task parallelization and focus on memory access optimization. All FPGA-based SW implementations [6][7][8][9][10][11][12][13][14][15][16][17][18][19][20] use the systolic array architecture as the basis for their designs. However, those implementations either simplify the scoring rules, or only take into account the scoring matrix calculations, or only support small scale sequence alignment with specific sequence type and scoring model.…”
Section: Discussionmentioning
confidence: 99%
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“…When two DNA strands are separated by an enzyme, a single strand messenger RNA, complementary to DNA strand, is formed by mapping from DNA sequences, which consist of A, T, C, G, to complementary RNA sequences, which consist of U, A, G, C. These process noncoding segments, called introns in DNA sequences, are removed by splicing and remaining segments that encode information for protein synthesis, called exons, are assembled in mRNA [10]. [10] DNA and RNA both share common codons; A, G, C. DNA has an additional T codon whereas RNA has an additional U codon.…”
Section: Dna Translation Transcriptionmentioning
confidence: 99%
“…[10] DNA and RNA both share common codons; A, G, C. DNA has an additional T codon whereas RNA has an additional U codon. Both these additional codons are used to form proteins.…”
Section: Dna Translation Transcriptionmentioning
confidence: 99%