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Alexander Cope

dblp:223/8056 · DBLP profile ↗
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2ranked-venue papers
1as first author
1since 2021 · last 2022
0000-0002-5756-7812ORCID · reported

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 · 92% Computational science and engineering · 8%

Topics — the 6 heaviest of 6, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › transcriptomics
ribosome profiling
0.722022
riboviz 2: a flexible and robust ribosome profiling data analysis and visualization workflow · Bioinform. 2022
AnaCoDa: analyzing codon data with Bayesian mixture models · Bioinform. 2018
Bioinformatics and computational biology › transcriptomics
ribo-seq data analysis
0.612022
riboviz 2: a flexible and robust ribosome profiling data analysis and visualization workflow · Bioinform. 2022
Bioinformatics and computational biology › molecular evolution
codon usage analysis
0.312018
AnaCoDa: analyzing codon data with Bayesian mixture models · Bioinform. 2018
Bioinformatics and computational biology › genomics
computational genomics
0.312018
AnaCoDa: analyzing codon data with Bayesian mixture models · Bioinform. 2018
Bioinformatics and computational biology
bioinformatics workflow
0.212022
riboviz 2: a flexible and robust ribosome profiling data analysis and visualization workflow · Bioinform. 2022
Computational science and engineering
workflow management
0.212022
riboviz 2: a flexible and robust ribosome profiling data analysis and visualization workflow · Bioinform. 2022

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

nextflow · 0.6mixture model · 0.3hierarchical modeling · 0.3Bayesian MCMC · 0.3
YearPublicationVenuePosition
2022 riboviz 2: a flexible and robust ribosome profiling data analysis and visualization workflow
abstract
MOTIVATION: Ribosome profiling, or Ribo-seq, is the state-of-the-art method for quantifying protein synthesis in living cells. Computational analysis of Ribo-seq data remains challenging due to the complexity of the procedure, as well as variations introduced for specific organisms or specialized analyses. RESULTS: We present riboviz 2, an updated riboviz package, for the comprehensive transcript-centric analysis and visualization of Ribo-seq data. riboviz 2 includes an analysis workflow built on the Nextflow workflow management system for end-to-end processing of Ribo-seq data. riboviz 2 has been extensively tested on diverse species and library preparation strategies, including multiplexed samples. riboviz 2 is flexible and uses open, documented file formats, allowing users to integrate new analyses with the pipeline. AVAILABILITY AND IMPLEMENTATION: riboviz 2 is freely available at github.com/riboviz/riboviz.
Alexander Cope, Felicity Anderson, John Favate, Amanda Mok, Anna Kurowska, Emma Mackenzie, Vikram Shivakumar, Peter Tilton, Sophie M. Winterbourne, Siyin Xue, Kostas Kavoussanakis, Liana F. Lareau, Premal Shah, Edward W. J. Wallace
Bioinform.1
2018 AnaCoDa: analyzing codon data with Bayesian mixture models
abstract
Summary: AnaCoDa is an R package for estimating biologically relevant parameters of mixture models, such as selection against translation inefficiency, non-sense errors and ribosome pausing time, from genomic and high throughput datasets. AnaCoDa provides an adaptive Bayesian MCMC algorithm, fully implemented in C++ for high performance with an ergonomic R interface to improve usability. AnaCoDa employs a generic object-oriented design to allow users to extend the framework and implement their own models. Current models implemented in AnaCoDa can accurately estimate biologically relevant parameters given either protein coding sequences or ribosome foot-printing data. Optionally, AnaCoDa can utilize additional data sources, such as gene expression measurements, to aid model fitting and parameter estimation. By utilizing a hierarchical object structure, some parameters can vary between sets of genes while others can be shared. Genes may be assigned to clusters or membership may be estimated by AnaCoDa. This flexibility allows users to estimate the same model parameter under different biological conditions and categorize genes into different sets based on shared model properties embedded within the data. AnaCoDa also allows users to generate simulated data which can be used to aid model development and model analysis as well as evaluate model adequacy. Finally, AnaCoDa contains a set of visualization routines and the ability to revisit or re-initiate previous model fitting, providing researchers with a well rounded easy to use framework to analyze genome scale data. Availability and implementation: AnaCoDa is freely available under the Mozilla Public License 2.0 on CRAN (https://cran.r-project.org/web/packages/AnaCoDa/).
Cedric Landerer, Alexander Cope, Russell Zaretzki, Michael A. Gilchrist
Bioinform.2