Demo Data from EDBT 2026 / reviewers in the wild / expert
Brad McNeney
dblp:99/6713
· DBLP profile ↗
2ranked-venue papers
0as first author
0since 2021 · last 2016
—ORCID · none
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 2
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 6 heaviest of 6, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology
population genetics |
0.3 | 2 | 2016 | Sampletrees and Rsampletrees: sampling gene genealogies conditional on SNP genotype data · Bioinform. 2016 Stepwise detection of recombination breakpoints in sequence alignments · Bioinform. 2005 |
Bioinformatics and computational biology
markov chain monte carlo |
0.2 | 1 | 2016 | Sampletrees and Rsampletrees: sampling gene genealogies conditional on SNP genotype data · Bioinform. 2016 |
Bioinformatics and computational biology › statistical genetics
genotype data analysis |
0.1 | 1 | 2016 | Sampletrees and Rsampletrees: sampling gene genealogies conditional on SNP genotype data · Bioinform. 2016 |
Bioinformatics and computational biology › genomics › genomic data management
genotype data management |
0.1 | 1 | 2016 | Sampletrees and Rsampletrees: sampling gene genealogies conditional on SNP genotype data · Bioinform. 2016 |
Bioinformatics and computational biology › molecular evolution
recombination breakpoint detection |
0.1 | 1 | 2005 | Stepwise detection of recombination breakpoints in sequence alignments · Bioinform. 2005 |
Bioinformatics and computational biology › molecular evolution
recombination detection |
0.1 | 1 | 2005 | Stepwise detection of recombination breakpoints in sequence alignments · Bioinform. 2005 |
Methods — techniques the papers use, named apart from their topics
markov chain monte carlo · 0.2permutation test · 0.1maximum chi-squared method · 0.1
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2016 | Sampletrees and Rsampletrees: sampling gene genealogies conditional on SNP genotype dataabstractUNLABELLED: : The program sampletrees is a Markov chain Monte Carlo sampler of gene genealogies conditional on either phased or unphased SNP genotype data. The companion program Rsampletrees is for pre- and post-processing of sampletrees files, including setting up the files for sampletrees and storing and plotting the output of a sampletrees run. AVAILABILITY AND IMPLEMENTATION: sampletrees is implemented in C ++. The source code, documentation and test files are available at http://stat.sfu.ca/statgen/research/sampletrees.html The R package Rsampletrees is available on CRAN http://cran.r-project.org/web/packages/Rsampletrees/index.html CONTACT: : [email protected] SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Kelly M. Burkett, Brad McNeney, Jinko Graham |
Bioinform. | 2 |
| 2005 | Stepwise detection of recombination breakpoints in sequence alignmentsabstractMOTIVATION: We propose a stepwise approach to identify recombination breakpoints in a sequence alignment. The approach can be applied to any recombination detection method that uses a permutation test and provides estimates of breakpoints. RESULTS: We illustrate the approach by analyses of a simulated dataset and alignments of real data from HIV-1 and human chromosome 7. The presented simulation results compare the statistical properties of one-step and two-step procedures. More breakpoints are found with a two-step procedure than with a single application of a given method, particularly for higher recombination rates. At higher recombination rates, the additional breakpoints were located at the cost of only a slight increase in the number of falsely declared breakpoints. However, a large proportion of breakpoints still go undetected. AVAILABILITY: A makefile and C source code for phylogenetic profiling and the maximum chi2 method, tested with the gcc compiler on Linux and WindowsXP, are available at http://stat-db.stat.sfu.ca/stepwise/ CONTACT: [email protected]. Jinko Graham, Brad McNeney, Françoise Seillier-Moiseiwitsch |
Bioinform. | 2 |