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J. T. Pedersen

dblp:72/5865 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 1992
—ORCID · none

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

Applied, 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.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › multiple sequence alignment
multiple sequence alignment analysis
0.011992
BIOSITE: a program for the interactive comparison of aligned homologous protein sequences · Comput. Appl. Biosci. 1992
Bioinformatics and computational biology
sequence alignment
0.011992
BIOSITE: a program for the interactive comparison of aligned homologous protein sequences · Comput. Appl. Biosci. 1992
Bioinformatics and computational biology
sequence analysis
0.011992
BIOSITE: a program for the interactive comparison of aligned homologous protein sequences · Comput. Appl. Biosci. 1992
Bioinformatics and computational biology › protein sequence analysis
sequence-function relationship
0.011992
BIOSITE: a program for the interactive comparison of aligned homologous protein sequences · Comput. Appl. Biosci. 1992

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

identity sequence generation · 0.0difference sequence generation · 0.0
YearPublicationVenuePosition
1992 BIOSITE: a program for the interactive comparison of aligned homologous protein sequences
abstract
A program, BIOSITE, providing for the interactive visual comparison of aligned homologous amino-acid sequences is presented, including an example of its application. The program allows for two types of comparison sequence to be generated: an 'identity' sequence and a 'difference' sequence. These may be used on subsets of sequences and in further comparisons to identify candidate sites involved in a distinct functional property. The program should prove a useful tool for biologists engaged in understanding sequence--function relationships.
V. B. Cockcroft, J. T. Pedersen, G. G. Lunt, David J. Osguthorpe
Comput. Appl. Biosci.2