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J. Gill Watt

dblp:40/3202 · DBLP profile ↗
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2ranked-venue papers
0as first author
0since 2021 · last 1993
—ORCID · none

Domains — the database's venue-derived domains; a paper can count in several

Systems, architecture and hardware · 1Applied, interdisciplinary, general and emerging computing · 1

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Computer architecture, parallel and distributed computing, and storage systems
1 paper
Hardware accelerators and domain-specific architectures · 100%
Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
sequence alignment
0.011993
A special-purpose processor for gene sequence analysis · Comput. Appl. Biosci. 1993
Hardware accelerators and domain-specific architectures
bioinformatics accelerator
0.011993
A special-purpose processor for gene sequence analysis · Comput. Appl. Biosci. 1993
Hardware accelerators and domain-specific architectures › bioinformatics accelerator
sequence alignment accelerator
0.011993
A special-purpose processor for gene sequence analysis · Comput. Appl. Biosci. 1993

Methods — techniques the papers use, named apart from their topics

custom hardware design · 0.0FPGA · 0.0
YearPublicationVenuePosition
1993 A special-purpose processor for gene sequence analysis
abstract
Advances in computational biology have occurred primarily in the areas of software and algorithm development; new designs of hardware to support biological computing are extremely scarce. This is due, we believe, to the presence of a non-trivial knowledge gap between molecular biologists and computer designers. The existence of this gap is unfortunate, as it has long been known that for certain problems, special-purpose computers can achieve significant cost/performance gains over general-purpose machines. We describe one such computer here: a custom accelerator for gene sequence analysis. The accelerator implements a version of the Needleman-Wunsch algorithm for nucleotide sequence alignment. Sequence lengths are constrained only by available memory; the product of sequence lengths in the current implementation can be up to 2(22). The machine is implemented as two NuBus boards connected to a Mac IIf/x, using a mixture of TTL and FPGA technology clocked at 10 MHz. The boards are completely functional, and yield a 15-fold performance improvement over an unassisted host.
Barry S. Fagin, J. Gill Watt, R. Gross
Comput. Appl. Biosci.2
1992 FPGA and Rapid Prototyping Technology Use in a Special Purpose Computer for Molecular Genetics
abstract
A custom accelerator for gene sequence analysis is described. The use of rapid prototyping technology, the key to producing a working system in a short amount of time, as well as field-programmable gate arrays (FPGAs) and in-house printed circuit board (PCB) prototyping, are discussed. Price-performance comparisons of the processor with other machines are offered. The processor is completely functional and yields a 15* performance improvement over an unassisted host.>
Barry S. Fagin, J. Gill Watt
ICCD2