Demo Data from EDBT 2026 / reviewers in the wild / expert
Sarath Chandra Dantu
dblp:410/7294
· DBLP profile ↗
2ranked-venue papers
0as first author
2since 2021 · last 2024
0000-0003-2019-5311ORCID · corroborated
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 2 · 2 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 · 65% Computational science and engineering · 35% |
Topics — the 4 heaviest of 4, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › molecular evolution
coevolution analysis |
0.8 | 1 | 2024 | PyCoM: a python library for large-scale analysis of residue-residue coevolution data · Bioinform. 2024 |
Computational science and engineering › computational chemistry › molecular simulation
molecular dynamics |
0.7 | 1 | 2023 | MDSubSampler: a posteriori sampling of important protein conformations from biomolecular simulations · Bioinform. 2023 |
Bioinformatics and computational biology
protein structure prediction |
0.2 | 1 | 2024 | PyCoM: a python library for large-scale analysis of residue-residue coevolution data · Bioinform. 2024 |
Bioinformatics and computational biology › protein structure prediction
residue contact prediction |
0.2 | 1 | 2024 | PyCoM: a python library for large-scale analysis of residue-residue coevolution data · Bioinform. 2024 |
Methods — techniques the papers use, named apart from their topics
statistical analysis · 0.8weighted sampling · 0.7stratified sampling · 0.7bootstrapping · 0.7
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2024 | PyCoM: a python library for large-scale analysis of residue-residue coevolution dataabstractMOTIVATION: Computational methods to detect correlated amino acid positions in proteins have become a valuable tool to predict intra- and inter-residue protein contacts, protein structures, and effects of mutation on protein stability and function. While there are many tools and webservers to compute coevolution scoring matrices, there is no central repository of alignments and coevolution matrices for large-scale studies and pattern detection leveraging on biological and structural annotations already available in UniProt. RESULTS: We present a Python library, PyCoM, which enables users to query and analyze coevolution matrices and sequence alignments of 457 622 proteins, selected from UniProtKB/Swiss-Prot database (length ≤ 500 residues), from a precompiled coevolution matrix database (PyCoMdb). PyCoM facilitates the development of statistical analyses of residue coevolution patterns using filters on biological and structural annotations from UniProtKB/Swiss-Prot, with simple access to PyCoMdb for both novice and advanced users, supporting Jupyter Notebooks, Python scripts, and a web API access. The resource is open source and will help in generating data-driven computational models and methods to study and understand protein structures, stability, function, and design. AVAILABILITY AND IMPLEMENTATION: PyCoM code is freely available from https://github.com/scdantu/pycom and PyCoMdb and the Jupyter Notebook tutorials are freely available from https://pycom.brunel.ac.uk. Philipp E. Glass, Sabriyeh Alibai, Alessandro Pandini, Sarath Chandra Dantu |
Bioinform. | 4 |
| 2023 | MDSubSampler: a posteriori sampling of important protein conformations from biomolecular simulationsabstractMOTIVATION: Molecular dynamics (MD) simulations have become routine tools for the study of protein dynamics and function. Thanks to faster GPU-based algorithms, atomistic and coarse-grained simulations are being used to explore biological functions over the microsecond timescale, yielding terabytes of data spanning multiple trajectories, thereby extracting relevant protein conformations without losing important information is often challenging. RESULTS: We present MDSubSampler, a Python library and toolkit for a posteriori subsampling of data from multiple trajectories. This toolkit provides access to uniform, random, stratified, weighted sampling, and bootstrapping sampling methods. Sampling can be performed under the constraint of preserving the original distribution of relevant geometrical properties. Possible applications include simulations post-processing, noise reduction, and structures selection for ensemble docking. AVAILABILITY AND IMPLEMENTATION: MDSubSampler is freely available at https://github.com/alepandini/MDSubSampler, along with guidance on installation and tutorials on how it can be used. Namir Oues, Sarath Chandra Dantu, Riktaben Jigarkumar Patel, Alessandro Pandini |
Bioinform. | 2 |