Language:
English
繁體中文
Help
回圖書館首頁
手機版館藏查詢
Login
Back
Switch To:
Labeled
|
MARC Mode
|
ISBD
FPGA acceleration of sequence analys...
~
Mahram, Atabak.
Linked to FindBook
Google Book
Amazon
博客來
FPGA acceleration of sequence analysis tools in bioinformatics.
Record Type:
Language materials, printed : Monograph/item
Title/Author:
FPGA acceleration of sequence analysis tools in bioinformatics./
Author:
Mahram, Atabak.
Description:
187 p.
Notes:
Source: Dissertation Abstracts International, Volume: 75-02(E), Section: B.
Contained By:
Dissertation Abstracts International75-02B(E).
Subject:
Engineering, Computer. -
Online resource:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3575302
ISBN:
9781303529764
FPGA acceleration of sequence analysis tools in bioinformatics.
Mahram, Atabak.
FPGA acceleration of sequence analysis tools in bioinformatics.
- 187 p.
Source: Dissertation Abstracts International, Volume: 75-02(E), Section: B.
Thesis (Ph.D.)--Boston University, 2013.
With 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.
ISBN: 9781303529764Subjects--Topical Terms:
1669061
Engineering, Computer.
FPGA acceleration of sequence analysis tools in bioinformatics.
LDR
:03123nam a2200313 4500
001
1964641
005
20141010092629.5
008
150210s2013 ||||||||||||||||| ||eng d
020
$a
9781303529764
035
$a
(MiAaPQ)AAI3575302
035
$a
AAI3575302
040
$a
MiAaPQ
$c
MiAaPQ
100
1
$a
Mahram, Atabak.
$3
2101130
245
1 0
$a
FPGA acceleration of sequence analysis tools in bioinformatics.
300
$a
187 p.
500
$a
Source: Dissertation Abstracts International, Volume: 75-02(E), Section: B.
500
$a
Adviser: Martin Herbordt.
502
$a
Thesis (Ph.D.)--Boston University, 2013.
520
$a
With 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.
520
$a
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.
520
$a
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 80x 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.
520
$a
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.
590
$a
School code: 0017.
650
4
$a
Engineering, Computer.
$3
1669061
650
4
$a
Biology, Bioinformatics.
$3
1018415
690
$a
0464
690
$a
0715
710
2
$a
Boston University.
$b
Electrical and Computer Engineering.
$3
2094969
773
0
$t
Dissertation Abstracts International
$g
75-02B(E).
790
$a
0017
791
$a
Ph.D.
792
$a
2013
793
$a
English
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3575302
based on 0 review(s)
Location:
ALL
電子資源
Year:
Volume Number:
Items
1 records • Pages 1 •
1
Inventory Number
Location Name
Item Class
Material type
Call number
Usage Class
Loan Status
No. of reservations
Opac note
Attachments
W9259640
電子資源
11.線上閱覽_V
電子書
EB
一般使用(Normal)
On shelf
0
1 records • Pages 1 •
1
Multimedia
Reviews
Add a review
and share your thoughts with other readers
Export
pickup library
Processing
...
Change password
Login