FPGA acceleration of sequence analysis tools in bioinformatics

Thesis (Ph.D.)--Boston UniversityWith advances in biotechnology and computing power, biological data are being produced at an exceptional rate. The purpose of this study is to analyze the application of FPGAs to accelerate high impact production biosequence analysis tools. Compared with other alternatives, FPGAs offer huge compute power, lower power consumption, and reasonable flexibility. BLAST has become the de facto standard in bioinformatic approximate string matching and so its acceleration is of fundamental importance. It is a complex highly-optimized system, consisting of tens of thousands of lines of code and a large number of heuristics. Our idea is to emulate the main phases of its algorithm on FPGA. Utilizing our FPGA engine, we quickly reduce the size of the database to a small fraction, and then use the original code to process the query. Using a standard FPGA-based system, we achieved 12x speedup over a highly optimized multithread reference code. Multiple Sequence Alignment (MSA)--the extension of pairwise Sequence Alignment to multiple Sequences--is critical to solve many biological problems. Previous attempts to accelerate Clustal-W, the most commonly used MSA code, have directly mapped a portion of the code to the FPGA. We use a new approach: we apply prefiltering of the kind commonly used in BLAST to perform the initial all-pairs alignments. This results in a speedup of from 8Ox to 190x over the CPU code (8 cores). The quality is comparable to the original according to a commonly used benchmark suite evaluated with respect to multiple distance metrics. The challenge in FPGA-based acceleration is finding a suitable application mapping. Unfortunately many software heuristics do not fall into this category and so other methods must be applied. One is restructuring: an entirely new algorithm is applied. Another is to analyze application utilization and develop accuracy/performance tradeoffs. Using our prefiltering approach and novel FPGA programming models we have achieved significant speedup over reference programs. We have applied approximation, seeding, and filtering to this end. The bulk of this study is to introduce the pros and cons of these acceleration models for biosequence analysis tools

FPGAs in Bioinformatics: Implementation and Evaluation of Common Bioinformatics Algorithms in Reconfigurable Logic

Life. Much effort is taken to grant humanity a little insight in this fascinating and complex but fundamental topic. In order to understand the relations and to derive consequences humans have begun to sequence their genomes, i.e. to determine their DNA sequences to infer information, e.g. related to genetic diseases. The process of DNA sequencing as well as subsequent analysis presents a computational challenge for recent computing systems due to the large amounts of data alone. Runtimes of more than one day for analysis of simple datasets are common, even if the process is already run on a CPU cluster. This thesis shows how this general problem in the area of bioinformatics can be tackled with reconfigurable hardware, especially FPGAs. Three compute intensive problems are highlighted: sequence alignment, SNP interaction analysis and genotype imputation. In the area of sequence alignment the software BLASTp for protein database searches is exemplarily presented, implemented and evaluated.SNP interaction analysis is presented with three applications performing an exhaustive search for interactions including the corresponding statistical tests: BOOST, iLOCi and the mutual information measurement. All applications are implemented in FPGA-hardware and evaluated, resulting in an impressive speedup of more than in three orders of magnitude when compared to standard computers. The last topic of genotype imputation presents a two-step process composed of the phasing step and the actual imputation step. The focus lies on the phasing step which is targeted by the SHAPEIT2 application. SHAPEIT2 is discussed with its underlying mathematical methods in detail, and finally implemented and evaluated. A remarkable speedup of 46 is reached here as well

High-Throughput DTW accelerator with minimum area in AMD FPGA by HLS.

Dynamic Time Warping (DTW) is a dynamic programming algorithm that is known to be one of the best methods to measure the similarities between two signals, even if there are variations in the speed of those. It is extensively used in many machine learning algorithms, especially for pattern recognition and classification. U nfortunately, i t h as a q uadratic complexity, which results in very high computational costs. Furthermore, its data dependency made it also very difficult t o parallelize. Special attention has been paid to computing DTW on the edge, as a way to reduce the load of communication on Internet-of- Thing applications. In this work, we propose a minimum area implementation of the DTW algorithm in AMD FPGAs with optimal use of the resources. That is achieved by maximizing the use time of the resources and taking advantage of the inner structure of the AMD FPGAs. This architecture could be used in small devices or as a base for a multi-core implementation with very high-throughput.MCIN/AEI/10.13039/501100011033and European Union Next Generation EU/PRTR under Project TED2021- 131527B-I00; by the Fondo Europeo de Desarrollo Regional (UMA20-FEDERJA-059); and by AMD™(Xilinx™) University Program Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tech

並列計算アクセラレータへの効率的なアプリケーションマッピングに関する研究

長崎大学学位論文 学位記番号:博(工)甲第3号 学位授与年月日:平成26年3月20日Nagasaki University (長崎大学)課程博

FPGAs in der Bioinformatik: Implementierung und Evaluierung bekannter bioinformatischer Algorithmen in rekonfigurierbarer Logik

Life. Much effort is taken to grant humanity a little insight in this fascinating and complex but fundamental topic. In order to understand the relations and to derive consequences humans have begun to sequence their genomes, i.e. to determine their DNA sequences to infer information, e.g. related to genetic diseases. The process of DNA sequencing as well as subsequent analysis presents a computational challenge for recent computing systems due to the large amounts of data alone. Runtimes of more than one day for analysis of simple datasets are common, even if the process is already run on a CPU cluster. This thesis shows how this general problem in the area of bioinformatics can be tackled with reconfigurable hardware, especially FPGAs. Three compute intensive problems are highlighted: sequence alignment, SNP interaction analysis and genotype imputation. In the area of sequence alignment the software BLASTp for protein database searches is exemplarily presented, implemented and evaluated. SNP interaction analysis is presented with three applications performing an exhaustive search for interactions including the corresponding statistical tests: BOOST, iLOCi and the mutual information measurement. All applications are implemented in FPGA-hardware and evaluated, resulting in an impressive speedup of more than in three orders of magnitude when compared to standard computers. The last topic of genotype imputation presents a two-step process composed of the phasing step and the actual imputation step. The focus lies on the phasing step which is targeted by the SHAPEIT2 application. SHAPEIT2 is discussed with its underlying mathematical methods in detail, and finally implemented and evaluated. A remarkable speedup of 46 is reached here as well.Das Leben. Sehr viel Aufwand wird getrieben um der Menschheit einen Einblick in dieses faszinierende und komplexe, aber fundamentale Thema zu erlauben. Um Zusammenhänge zu verstehen und Folgen ableiten zu können hat der Mensch begonnen sein Genom zu sequenzieren, d.h. seine DNA zu bestimmen um daraus Informationen, z.B. in Bezug auf Erbkrankheiten folgern zu können. Der Prozess der DNA-Sequenzierung sowie die darauffolgenden Analysen sind schon allein wegen der riesigen Datenmengen eine Herausforderung für aktuelle Rechensysteme. Laufzeiten von über einen Tag für die Analyse einfacher Datensätze sind üblich, selbst wenn der Prozess bereits auf einem Computercluster ausgeführt wird. Diese Arbeit zeigt, wie dieses gängige Problem im Bereich der Bioinformatik mit rekonfigurierbarer Hardware, speziell FPGAs, angegangen werden kann. Es werden drei rechenintensive Themengebiete hervorgehoben: Sequenzalignment, SNP-Interaktionsanalyse und Genotyp-Imputation. Beispielhaft wird im Bereich des Sequenzalignments die Software BLASTp für die Suche in Proteinsequenzdatenbanken vorgestellt, implementiert und evaluiert. Die SNP-Interaktionsanalyse wird mit drei Verfahren zur vollständigen Suche von Interaktionen inklusive des dazugehörigen statistischen Tests vorgestellt: BOOST, iLOCi und die Messung der Transinformation. Alle Verfahren werden auf FPGA-Hardware implementiert und evaluiert, mit einer bestechenden Beschleunigung im dreistelligen Bereich gegenüber Standard-Rechnern. Das letzte Gebiet der Genotyp-Imputierung ist ein zweiteiliges Verfahren bestehend aus dem Phasing und der eigentlichen Imputation. Der Schwerpunkt liegt im Phasing-Schritt, der mit dem SHAPEIT2-Tool adressiert wird. SHAPEIT2 wird ausführlich mit den zugrunde liegenden mathematischen Methoden diskutiert, und schließlich implementiert und evaluiert. Auch hier wird ein beachtlicher Speedup von 46 erreicht

Trace-based Performance Analysis for Hardware Accelerators

This thesis presents how performance data from hardware accelerators can be included in event logs. It extends the capabilities of trace-based performance analysis to also monitor and record data from this novel parallelization layer. The increasing awareness to power consumption of computing devices has led to an interest in hybrid computing architectures as well. High-end computers, workstations, and mobile devices start to employ hardware accelerators to offload computationally intense and parallel tasks, while at the same time retaining a highly efficient scalar compute unit for non-parallel tasks. This execution pattern is typically asynchronous so that the scalar unit can resume other work while the hardware accelerator is busy. Performance analysis tools provided by the hardware accelerator vendors cover the situation of one host using one device very well. Yet, they do not address the needs of the high performance computing community. This thesis investigates ways to extend existing methods for recording events from highly parallel applications to also cover scenarios in which hardware accelerators aid these applications. After introducing a generic approach that is suitable for any API based acceleration paradigm, the thesis derives a suggestion for a generic performance API for hardware accelerators and its implementation with NVIDIA CUPTI. In a next step the visualization of event logs containing data from execution streams on different levels of parallelism is discussed. In order to overcome the limitations of classic performance profiles and timeline displays, a graph-based visualization using Parallel Performance Flow Graphs (PPFGs) is introduced. This novel technical approach is using program states in order to display similarities and differences between the potentially very large number of event streams and, thus, enables a fast way to spot load imbalances. The thesis concludes with the in-depth analysis of a case-study of PIConGPU---a highly parallel, multi-hybrid plasma physics simulation---that benefited greatly from the developed performance analysis methods.Diese Dissertation zeigt, wie der Ablauf von Anwendungsteilen, die auf Hardwarebeschleuniger ausgelagert wurden, als Programmspur mit aufgezeichnet werden kann. Damit wird die bekannte Technik der Leistungsanalyse von Anwendungen mittels Programmspuren so erweitert, dass auch diese neue Parallelitätsebene mit erfasst wird. Die Beschränkungen von Computersystemen bezüglich der elektrischen Leistungsaufnahme hat zu einer steigenden Anzahl von hybriden Computerarchitekturen geführt. Sowohl Hochleistungsrechner, aber auch Arbeitsplatzcomputer und mobile Endgeräte nutzen heute Hardwarebeschleuniger um rechenintensive, parallele Programmteile auszulagern und so den skalaren Hauptprozessor zu entlasten und nur für nicht parallele Programmteile zu verwenden. Dieses Ausführungsschema ist typischerweise asynchron: der Skalarprozessor kann, während der Hardwarebeschleuniger rechnet, selbst weiterarbeiten. Die Leistungsanalyse-Werkzeuge der Hersteller von Hardwarebeschleunigern decken den Standardfall (ein Host-System mit einem Hardwarebeschleuniger) sehr gut ab, scheitern aber an einer Unterstützung von hochparallelen Rechnersystemen. Die vorliegende Dissertation untersucht, in wie weit auch multi-hybride Anwendungen die Aktivität von Hardwarebeschleunigern aufzeichnen können. Dazu wird die vorhandene Methode zur Erzeugung von Programmspuren für hochparallele Anwendungen entsprechend erweitert. In dieser Untersuchung wird zuerst eine allgemeine Methodik entwickelt, mit der sich für jede API-gestützte Hardwarebeschleunigung eine Programmspur erstellen lässt. Darauf aufbauend wird eine eigene Programmierschnittstelle entwickelt, die es ermöglicht weitere leistungsrelevante Daten aufzuzeichnen. Die Umsetzung dieser Schnittstelle wird am Beispiel von NVIDIA CUPTI darstellt. Ein weiterer Teil der Arbeit beschäftigt sich mit der Darstellung von Programmspuren, welche Aufzeichnungen von den unterschiedlichen Parallelitätsebenen enthalten. Um die Einschränkungen klassischer Leistungsprofile oder Zeitachsendarstellungen zu überwinden, wird mit den parallelen Programmablaufgraphen (PPFGs) eine neue graphenbasisierte Darstellungsform eingeführt. Dieser neuartige Ansatz zeigt eine Programmspur als eine Folge von Programmzuständen mit gemeinsamen und unterchiedlichen Abläufen. So können divergierendes Programmverhalten und Lastimbalancen deutlich einfacher lokalisiert werden. Die Arbeit schließt mit der detaillierten Analyse von PIConGPU -- einer multi-hybriden Simulation aus der Plasmaphysik --, die in großem Maße von den in dieser Arbeit entwickelten Analysemöglichkeiten profiert hat

Efficiently and Transparently Maintaining High SIMD Occupancy in the Presence of Wavefront Irregularity

Demand is increasing for high throughput processing of irregular streaming applications; examples of such applications from scientific and engineering domains include biological sequence alignment, network packet filtering, automated face detection, and big graph algorithms. With wide SIMD, lightweight threads, and low-cost thread-context switching, wide-SIMD architectures such as GPUs allow considerable flexibility in the way application work is assigned to threads. However, irregular applications are challenging to map efficiently onto wide SIMD because data-dependent filtering or replication of items creates an unpredictable data wavefront of items ready for further processing. Straightforward implementations of irregular applications on a wide-SIMD architecture are prone to load imbalance and reduced occupancy, while more sophisticated implementations require advanced use of parallel GPU operations to redistribute work efficiently among threads. This dissertation will present strategies for addressing the performance challenges of wavefront- irregular applications on wide-SIMD architectures. These strategies are embodied in a developer framework called Mercator that (1) allows developers to map irregular applications onto GPUs ac- cording to the streaming paradigm while abstracting from low-level data movement and (2) includes generalized techniques for transparently overcoming the obstacles to high throughput presented by wavefront-irregular applications on a GPU. Mercator forms the centerpiece of this dissertation, and we present its motivation, performance model, implementation, and extensions in this work

High Performance Computing for DNA Sequence Alignment and Assembly

Recent advances in DNA sequencing technology have dramatically increased the scale and scope of DNA sequencing. These data are used for a wide variety of important biological analyzes, including genome sequencing, comparative genomics, transcriptome analysis, and personalized medicine but are complicated by the volume and complexity of the data involved. Given the massive size of these datasets, computational biology must draw on the advances of high performance computing. Two fundamental computations in computational biology are read alignment and genome assembly. Read alignment maps short DNA sequences to a reference genome to discover conserved and polymorphic regions of the genome. Genome assembly computes the sequence of a genome from many short DNA sequences. Both computations benefit from recent advances in high performance computing to efficiently process the huge datasets involved, including using highly parallel graphics processing units (GPUs) as high performance desktop processors, and using the MapReduce framework coupled with cloud computing to parallelize computation to large compute grids. This dissertation demonstrates how these technologies can be used to accelerate these computations by orders of magnitude, and have the potential to make otherwise infeasible computations practical

Transcript assembly and abundance estimation with high-throughput RNA sequencing

We present algorithms and statistical methods for the reconstruction and abundance estimation of transcript sequences from high throughput RNA sequencing ("RNA-Seq"). We evaluate these approaches through large-scale experiments of a well studied model of muscle development. We begin with an overview of sequencing assays and outline why the short read alignment problem is fundamental to the analysis of these assays. We then describe two approaches to the contiguous alignment problem, one of which uses massively parallel graphics hardware to accelerate alignment, and one of which exploits an indexing scheme based on the Burrows-Wheeler transform. We then turn to the spliced alignment problem, which is fundamental to RNA-Seq, and present an algorithm, TopHat. TopHat is the first algorithm that can align the reads from an entire RNA-Seq experiment to a large genome without the aid of reference gene models. In the second part of the thesis, we present the first comparative RNA-Seq as- sembly algorithm, Cufflinks, which is adapted from a constructive proof of Dilworth's Theorem, a classic result in combinatorics. We evaluate Cufflinks by assembling the transcriptome from a time course RNA-Seq experiment of developing skeletal muscle cells. The assembly contains 13,689 known transcripts and 3,724 novel ones. Of the novel transcripts, 62% were strongly supported by earlier sequencing experiments or by homologous transcripts in other organisms. We further validated interesting genes with isoform-specific RT-PCR. We then present a statistical model for RNA-Seq included in Cufflinks and with which we estimate abundances of transcripts from RNA-seq data. Simulation studies demonstrate that the model is highly accurate. We apply this model to the muscle data, and track the abundances of individual isoforms over development. Finally, we present significance tests for changes in relative and absolute abundances between time points, which we employ to uncover differential expression and differential regulation. By testing for relative abundance changes within and between transcripts sharing a transcription start site, we find significant shifts in the rates of alternative splicing and promoter preference in hundreds of genes, including those believed to regulate muscle development