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Lina Weinbrand

dblp:136/6120 · DBLP profile ↗
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1ranked-venue papers
1as first author
0since 2021 · last 2013
—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 2 heaviest of 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › RNA biology › RNA analysis › RNA bioinformatics › RNA design
RNA inverse folding
0.212013
RNAfbinv: an interactive Java application for fragment-based design of RNA sequences · Bioinform. 2013
Bioinformatics and computational biology › RNA biology › RNA analysis › RNA bioinformatics › RNA structure
RNA secondary structure
0.012013
RNAfbinv: an interactive Java application for fragment-based design of RNA sequences · Bioinform. 2013

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

thermodynamic stability optimization · 0.2mutational robustness · 0.2
YearPublicationVenuePosition
2013 RNAfbinv: an interactive Java application for fragment-based design of RNA sequences
abstract
SUMMARY: In RNA design problems, it is plausible to assume that the user would be interested in preserving a particular RNA secondary structure motif, or fragment, for biological reasons. The preservation could be in structure or sequence, or both. Thus, the inverse RNA folding problem could benefit from considering fragment constraints. We have developed a new interactive Java application called RNA fragment-based inverse that allows users to insert an RNA secondary structure in dot-bracket notation. It then performs sequence design that conforms to the shape of the input secondary structure, the specified thermodynamic stability, the specified mutational robustness and the user-selected fragment after shape decomposition. In this shape-based design approach, specific RNA structural motifs with known biological functions are strictly enforced, while others can possess more flexibility in their structure in favor of preserving physical attributes and additional constraints. AVAILABILITY: RNAfbinv is freely available for download on the web at http://www.cs.bgu.ac.il/~RNAexinv/RNAfbinv. The site contains a help file with an explanation regarding the exact use.
Lina Weinbrand, Assaf Avihoo, Danny Barash
Bioinform.1