Following publication of the original article [1], the author requested changes to the figures 4, 7, 8, 9, 12 and 14 to align these with the text. The corrected figures are supplied below. The original article [1] has been corrected. [Typesetter, please insert new supplied figure in package].

@en

BACKGROUND: Due the computational complexity of sequence alignment algorithms, various accelerated solutions have been proposed to speedup this analysis. NVBIO is the only available GPU library that accelerates sequence alignment of high-throughput NGS data, but has limited performance. In this article we present GASAL2, a GPU library for aligning DNA and RNA sequences that outperforms existing CPU and GPU libraries. RESULTS: The GASAL2 library provides specialized, accelerated kernels for local, global and all types of semi-global alignment. Pairwise sequence alignment can be performed with and without traceback. GASAL2 outperforms the fastest CPU-optimized SIMD implementations such as SeqAn and Parasail, as well as NVIDIA's own GPU-based library known as NVBIO. GASAL2 is unique in performing sequence packing on GPU, which is up to 750x faster than NVBIO. Overall on Geforce GTX 1080 Ti GPU, GASAL2 is up to 21x faster than Parasail on a dual socket hyper-threaded Intel Xeon system with 28 cores and up to 13x faster than NVBIO with a query length of up to 300 bases and 100 bases, respectively. GASAL2 alignment functions are asynchronous/non-blocking and allow full overlap of CPU and GPU execution. The paper shows how to use GASAL2 to accelerate BWA-MEM, speeding up the local alignment by 20x, which gives an overall application speedup of 1.3x vs. CPU with up to 12 threads. CONCLUSIONS: The library provides high performance APIs for local, global and semi-global alignment that can be easily integrated into various bioinformatics tools.

@en

Background: Pairwise sequence alignment is widely used in many biological tools and applications. Existing GPU accelerated implementations mainly focus on calculating optimal alignment score and omit identifying the optimal alignment itself. In GATK HaplotypeCaller (HC), the semi-global pairwise sequence alignment with traceback has so far
been difficult to accelerate effectively on GPUs.
Results: We first analyze the characteristics of the semi-global alignment with traceback in GATK HC and then propose a new algorithm that allows for retrieving the optimal alignment efficiently on GPUs. For the first stage, we choose intra-task parallelization model to calculate the position of the optimal alignment score and the backtracking matrix. Moreover, in the first stage, our GPU implementation also records the length of consecutive matches/mismatches in
addition to lengths of consecutive insertions and deletions as in the CPU-based implementation. This helps efficiently
retrieve the backtracking matrix to obtain the optimal alignment in the second stage.
Conclusions: Experimental results show that our alignment kernel with traceback is up to 80x and 14.14x faster than its CPU counterpart with synthetic datasets and real datasets, respectively. When integrated into GATK HC (alongside a GPU accelerated pair-HMMs forward kernel), the overall acceleration is 2.3x faster than the baseline GATK HC
implementation, and 1.34x faster than the GATK HC implementation with the integrated GPU-based pair-HMMs forward algorithm. Although the methods proposed in this paper is to improve the performance of GATK HC, they can also be used in other pairwise alignments and applications.@en

In order to improve the accuracy of indel detection, micro-assembly is used in multiple variant callers, such as the GATK HaplotypeCaller to reassemble reads in a specific region of the genome. Assembly is a computationally intensive process that causes runtime bottlenecks. In this paper, we propose a GPU-based de Bruijn graph construction algorithm for micro-assembly in the GATK HaplotypeCaller to improve its performance. Various synthetic datasets are used to compare the performance of the GPU-based de Bruijn graph construction implementation with the software-only baseline, which achieves a speedup of up to 3x. An experiment using two human genome datasets is used to evaluate the performance shows a speedup of up to 2.66x.@en

GATK HaplotypeCaller (HC) is a popular variant caller, which is widely used to identify variants in complex genomes. However, due to its high variants detection accuracy, it suffers from long execution time. In GATK HC, the pair-HMMs forward algorithm accounts for a large percentage of the total execution time. This article proposes to accelerate the pair-HMMs forward algorithm on graphics processing units (GPUs) to improve the performance of GATK HC. This article presents several GPU-based implementations of the pair-HMMs forward algorithm. It also analyzes the performance bottlenecks of the implementations on an NVIDIA Tesla K40 card with various data sets. Based on these results and the characteristics of GATK HC, we are able to identify the GPU-based implementations with the highest performance for the various analyzed data sets. Experimental results show that the GPU-based implementations of the pair-HMMs forward algorithm achieve a speedup of up to 5.47× over existing GPU-based implementations.@en

Due to its high-throughput and low cost, Next Generation Sequencing (NGS) technology is becoming increasingly popular in many genomics research labs. However, handling the massive raw data generated by the NGS platforms poses a significant computational challenge to genomics analysis tools. This paper presents a GPU acceleration of the GATK HaplotypeCaller (GATK HC), a widely used DNA variant caller in the clinic. Moreover, this paper proposes a load-balanced multi-process optimization of GATK HaplotypeCaller to address its implementation limitation which forces the sequential execution of the program and prevents effective utilization of hardware acceleration. In single-threaded mode, the GPU-based GATK HC is 1.71x and 1.21x faster than the baseline HC implementation and the vectorized GATK HC implementation, respectively. Moreover, the GPU-based implementation achieves up to 2.04x and 1.40x speedup in load-balanced multi-process mode over the baseline implementation and the vectorized GATK HC implementation in non-load-balanced multi-process mode, respectively.@en

In the analysis of next-generation DNA sequencing data, Hidden Markov Models (HMMs) are used to perform variant calling between DNA sequences and a reference genome. The PairHMM model is solved by the Forward Algorithm, for which the performance and power efficiency can be increased tremendously using systolic arrays (SAs) in FPGAs. We model the performance characteristics of such SAs, and propose a novel architecture that allows the computational units to continuously perform useful work on the input data. The implementation achieves up to 90\% of the theoretical throughput for a real dataset. The implementation of the proposed architecture achieves more than 2.5x throughput over the state-of-the-art on a similar contemporary platform.@en

In order to handle the massive raw data generated by next generation sequencing (NGS) platforms, GPUs are widely used by many genetic analysis tools to speed up the used algorithms. In this paper, we use GPUs to accelerate the pair-HMMs forward algorithm, which is used to calculate the overall alignment probability in many genomics analysis tools. We firstly evaluate two different implementation methods to accelerate the pair-HMMs forward algorithm according to their effectiveness on GPU platforms. Based on these two methods, we present several implementations of the pair-HMMs forward algorithm.
We execute these implementations on the NVIDIA Tesla K40 card using different datasets to compare the performance. Experimental results show that the intra-task implementation has the highest throughput in most cases, achieving pure computational throughput as high as 23.56 GCUPS for synthetic datasets.
On a real dataset, the inter-task implementation achieves 4.82x speedup compared with a vectorized implementation executed on a 20-core POWER8 system.@en

Many DNA sequence analysis tools have been developed to turn the massive raw DNA sequencing data generated by NGS (Next Generation Sequencing) platforms into biologically meaningful information. The pair-HMMs forward algorithm is widely used to calculate the overall alignment probability needed by a number of DNA analysis tools. In this paper, we propose a novel systolic array design to accelerate the pair-HMMs forward algorithm on FPGAs. A number of architectural features have been implemented to improve the performance of the design, such as early exit points to increase the utilization of the array for small sequence sizes, as well as on-chip buffering to enable the processing of long sequences effectively. We present an implementation of the design on the Convey supercomputing platform. Experimental results show that the FPGA implementation of the pair-HMMs forward algorithm is up to 67x faster, compared to software-only execution.@en