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Kelly M. Burkett

dblp:180/9744 · DBLP profile ↗
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2ranked-venue papers
1as first author
1since 2021 · last 2023
0000-0002-9488-5588ORCID · corroborated

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 · 100%

Topics — the 5 heaviest of 5, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
population genetics
0.922023
GENLIB: new function to simulate haplotype transmission in large complex genealogies · Bioinform. 2023
Sampletrees and Rsampletrees: sampling gene genealogies conditional on SNP genotype data · Bioinform. 2016
Bioinformatics and computational biology
statistical genetics
0.712023
GENLIB: new function to simulate haplotype transmission in large complex genealogies · Bioinform. 2023
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

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

monte carlo simulation · 0.7markov chain monte carlo · 0.2
YearPublicationVenuePosition
2023 GENLIB: new function to simulate haplotype transmission in large complex genealogies
abstract
SUMMARY: Founder populations with deep genealogical data are well suited for investigating genetic variants contributing to diseases. Here, we present a major update of the genealogical analysis R package GENLIB, centered around a new function which can simulate the transmission of haplotypes from founders to probands along very large and complex user-specified genealogies. AVAILABILITY AND IMPLEMENTATION: The latest update of the GENLIB package (v1.1.9) contains the new gen.simuHaplo() function and is available on the CRAN repository and from https://github.com/R-GENLIB/GENLIB. Examples can be accessed at https://github.com/R-GENLIB/simuhaplo_functions.
Mohan Rakesh, Hélène Vézina, Catherine Laprise, Ellen E. Freeman, Kelly M. Burkett, Marie-Hélène Roy-Gagnon
Bioinform.5
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.1