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Brad McNeney

dblp:99/6713 · DBLP profile ↗
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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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
population genetics
0.322016
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
0.212016
Sampletrees and Rsampletrees: sampling gene genealogies conditional on SNP genotype data · Bioinform. 2016
Bioinformatics and computational biology › statistical genetics
genotype data analysis
0.112016
Sampletrees and Rsampletrees: sampling gene genealogies conditional on SNP genotype data · Bioinform. 2016
Bioinformatics and computational biology › genomics › genomic data management
genotype data management
0.112016
Sampletrees and Rsampletrees: sampling gene genealogies conditional on SNP genotype data · Bioinform. 2016
Bioinformatics and computational biology › molecular evolution
recombination breakpoint detection
0.112005
Stepwise detection of recombination breakpoints in sequence alignments · Bioinform. 2005
Bioinformatics and computational biology › molecular evolution
recombination detection
0.112005
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
YearPublicationVenuePosition
2016 Sampletrees and Rsampletrees: sampling gene genealogies conditional on SNP genotype data
abstract
UNLABELLED: : 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 alignments
abstract
MOTIVATION: 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