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Mehari B. Zerihun

dblp:276/1587 · DBLP profile ↗
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2ranked-venue papers
1as first author
1since 2021 · last 2024
—ORCID · none

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

Applied, interdisciplinary, general and emerging computing · 2 · 1 first-author · 1 since 2021

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
2 papers
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 › statistical genetics
variant effect prediction
0.812024
pycofitness - Evaluating the fitness landscape of RNA and protein sequences · Bioinform. 2024
Bioinformatics and computational biology › protein structure prediction
direct coupling analysis
0.412020
pydca v1.0: a comprehensive software for direct coupling analysis of RNA and protein sequences · Bioinform. 2020
Bioinformatics and computational biology
protein structure prediction
0.112020
pydca v1.0: a comprehensive software for direct coupling analysis of RNA and protein sequences · Bioinform. 2020
Bioinformatics and computational biology › protein structure prediction
residue contact prediction
0.112020
pydca v1.0: a comprehensive software for direct coupling analysis of RNA and protein sequences · Bioinform. 2020

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

pseudo-likelihood maximization · 1.2direct coupling analysis · 0.8coevolution · 0.8mean-field approximation · 0.4inverse statistical approach · 0.4
YearPublicationVenuePosition
2024 pycofitness - Evaluating the fitness landscape of RNA and protein sequences
abstract
MOTIVATION: The accurate prediction of how mutations change biophysical properties of proteins or RNA is a major goal in computational biology with tremendous impacts on protein design and genetic variant interpretation. Evolutionary approaches such as coevolution can help solving this issue. RESULTS: We present pycofitness, a standalone Python-based software package for the in silico mutagenesis of protein and RNA sequences. It is based on coevolution and, more specifically, on a popular inverse statistical approach, namely direct coupling analysis by pseudo-likelihood maximization. Its efficient implementation and user-friendly command line interface make it an easy-to-use tool even for researchers with no bioinformatics background. To illustrate its strengths, we present three applications in which pycofitness efficiently predicts the deleteriousness of genetic variants and the effect of mutations on protein fitness and thermodynamic stability. AVAILABILITY AND IMPLEMENTATION: https://github.com/KIT-MBS/pycofitness.
Fabrizio Pucci, Mehari B. Zerihun, Marianne Rooman, Alexander Schug
Bioinform.2
2020 pydca v1.0: a comprehensive software for direct coupling analysis of RNA and protein sequences
abstract
MOTIVATION: The ongoing advances in sequencing technologies have provided a massive increase in the availability of sequence data. This made it possible to study the patterns of correlated substitution between residues in families of homologous proteins or RNAs and to retrieve structural and stability information. Direct coupling analysis (DCA) infers coevolutionary couplings between pairs of residues indicating their spatial proximity, making such information a valuable input for subsequent structure prediction. RESULTS: Here, we present pydca, a standalone Python-based software package for the DCA of protein- and RNA-homologous families. It is based on two popular inverse statistical approaches, namely, the mean-field and the pseudo-likelihood maximization and is equipped with a series of functionalities that range from multiple sequence alignment trimming to contact map visualization. Thanks to its efficient implementation, features and user-friendly command line interface, pydca is a modular and easy-to-use tool that can be used by researchers with a wide range of backgrounds. AVAILABILITY AND IMPLEMENTATION: pydca can be obtained from https://github.com/KIT-MBS/pydca or from the Python Package Index under the MIT License. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Mehari B. Zerihun, Fabrizio Pucci, Emanuel K. Peter, Alexander Schug
Bioinform.1