Demo Data from EDBT 2026 / reviewers in the wild / expert
Sara Rocha
dblp:95/10584
· DBLP profile ↗
2ranked-venue papers
0as first author
0since 2021 · last 2018
0000-0002-9705-1511ORCID · reported
Domains — the database's venue-derived domains; a paper can count in several
Computer networks · 1Applied, 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 2 heaviest of 3, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › next-generation sequencing
next-generation sequencing simulation |
0.3 | 1 | 2018 | NGSphy: phylogenomic simulation of next-generation sequencing data · Bioinform. 2018 |
Bioinformatics and computational biology › phylogenetics
phylogenomics |
0.3 | 1 | 2018 | NGSphy: phylogenomic simulation of next-generation sequencing data · Bioinform. 2018 |
Methods — techniques the papers use, named apart from their topics
statistical distribution sampling · 0.3
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2018 | NGSphy: phylogenomic simulation of next-generation sequencing dataabstractMotivation: Advances in sequencing technologies have made it feasible to obtain massive datasets for phylogenomic inference, often consisting of large numbers of loci from multiple species and individuals. The phylogenomic analysis of next-generation sequencing (NGS) data requires a complex computational pipeline where multiple technical and methodological decisions are necessary that can influence the final tree obtained, like those related to coverage, assembly, mapping, variant calling and/or phasing. Results: To assess the influence of these variables we introduce NGSphy, an open-source tool for the simulation of Illumina reads/read counts obtained from haploid/diploid individual genomes with thousands of independent gene families evolving under a common species tree. In order to resemble real NGS experiments, NGSphy includes multiple options to model sequencing coverage (depth) heterogeneity across species, individuals and loci, including off-target or uncaptured loci. For comprehensive simulations covering multiple evolutionary scenarios, parameter values for the different replicates can be sampled from user-defined statistical distributions. Availability and implementation: Source code, full documentation and tutorials including a 'Getting started' guide are available at http://github.com/merlyescalona/ngsphy. Supplementary information: Supplementary data are available at Bioinformatics online. Merly Escalona, Sara Rocha, David Posada |
Bioinform. | 2 |
| 2011 | From Mobile Computers to Mobile Information? A Case Study of Physicians' Mobile Information UseabstractPhysicians are faced with questions and uncertainties regarding information/knowledge for the best care of their patients. There are several sources of medical information available from which they can retrieve the necessary answers, such as colleagues, textbooks or software on personal digital assistants (PDA). This case study evaluates how physicians seek medical knowledge when they face a clinical challenge. Our observational study took place in one of the US Veterans Affair (VA) Hospitals, during August 2006, with combined observation of, and interviews with, physicians. Search for information was significantly different in strategy and materials used depending on location, temporality and complexity of the question. Daniel Ferreira 0004, Sara Rocha, João Santos 0003, Susan Hauser, Henrique M. G. Martins |
ICC | 2 |