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I. S. Pika

dblp:96/4769 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 1997
—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 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
multiple sequence alignment
0.011997
ProMSED: protein multiple sequence editor for Windows 3.11/95 · Comput. Appl. Biosci. 1997
Bioinformatics and computational biology › sequence alignment
sequence alignment editing
0.011997
ProMSED: protein multiple sequence editor for Windows 3.11/95 · Comput. Appl. Biosci. 1997
Bioinformatics and computational biology
sequence analysis
0.011997
ProMSED: protein multiple sequence editor for Windows 3.11/95 · Comput. Appl. Biosci. 1997

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

clustalv · 0.0
YearPublicationVenuePosition
1997 ProMSED: protein multiple sequence editor for Windows 3.11/95
abstract
MOTIVATION: Most protein sequence alignment algorithms give similar results on closely related proteins, while manual intervention may be needed for distantly related molecules. To correct the alignment, it is often necessary to repeat calculations on selected parts of the alignments and edit the alignment manually. Software implementing such interactive alignment procedures is of significance. RESULTS: This paper presents a new MS Windows application called ProMSED for both automatic and manual protein sequence alignment. The program reads main sequence formats and has a user-friendly interface. ProMSED performs automatic (ClustalV algorithm) alignments, alignment visualization and editing, and it allows sequences to be aligned interactively leaving previously aligned regions unchanged. Manual alignment and sequence analysis are facilitated by colouring schemes reflecting amino acid similarity of mutational and physicochemical properties. The interactive alignment of a diverged set of reverse transcriptases has located four out of six known conserved motifs. AVAILABILITY: ProMSED is available on request from the authors. DEMO is available from ftp://ftp.ebi.ac.uk/pub/ software/dos/promsed/ or ftp://iubio.bio.indiana.edu/molbio/ ibmpc/.
Anatoly S. Frolov, I. S. Pika, A. M. Eroshkin
Comput. Appl. Biosci.2