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R. D. Shortridge

dblp:12/6993 · DBLP profile ↗
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1ranked-venue papers
1as first author
0since 2021 · last 1986
—ORCID · none

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

Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author

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 › genome annotation
gene prediction
0.011986
IBM microcomputer programs that analyze DNA sequences for tRNA genes · Comput. Appl. Biosci. 1986
Bioinformatics and computational biology › genome annotation › gene prediction
tRNA gene search
0.011986
IBM microcomputer programs that analyze DNA sequences for tRNA genes · Comput. Appl. Biosci. 1986
Bioinformatics and computational biology › RNA biology › RNA analysis › RNA bioinformatics › RNA structure prediction
RNA secondary structure prediction
0.011986
IBM microcomputer programs that analyze DNA sequences for tRNA genes · Comput. Appl. Biosci. 1986
Bioinformatics and computational biology
sequence analysis
0.011986
IBM microcomputer programs that analyze DNA sequences for tRNA genes · Comput. Appl. Biosci. 1986

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

nearest-neighbor model · 0.0graphical plotting · 0.0
YearPublicationVenuePosition
1986 IBM microcomputer programs that analyze DNA sequences for tRNA genes
abstract
A set of four computer programs that search DNA sequence data files for transfer RNA genes have been written in IBM (Microsoft) BASIC for the IBM personal computer. These programs locate and plot predicted secondary structures of tRNA genes in the cloverleaf conformation. The set of programs are applicable to eukaryotic tRNA genes, including those containing intervening sequences, and to prokaryotic and mitochondrial tRNA genes. In addition, two of the programs search up to 150 residues downstream of tRNA gene sequences for possible eukaryotic RNA polymerase III termination sites comprised of at least four consecutive T residues. Molecular biologists studying a variety of gene sequence and flanking regions can use these programs to search for the additional presence of tRNA genes. Furthermore, investigators studying tRNA gene structure-to-function relationships would not need to do extensive restriction mapping to locate tRNA gene sequences within their cloned DNA fragments.
R. D. Shortridge, I. L. Pirtle, R. M. Pirtle
Comput. Appl. Biosci.1