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Alexander Braunstein

dblp:44/2381 · DBLP profile ↗
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1ranked-venue papers
1as first author
0since 2021 · last 2008
—ORCID · none

Domains — the database's venue-derived domains; a paper can count in several

Artificial intelligence and machine learning · 1 · 1 first-author

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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › population genetics › coalescent theory
coalescent model
0.112008
A spatially varying two-sample recombinant coalescent, with applications to HIV escape response · NIPS 2008
Bioinformatics and computational biology
phylogenetics
0.112008
A spatially varying two-sample recombinant coalescent, with applications to HIV escape response · NIPS 2008
Bioinformatics and computational biology › population genetics
recombination
0.112008
A spatially varying two-sample recombinant coalescent, with applications to HIV escape response · NIPS 2008
Bioinformatics and computational biology › molecular evolution
viral evolution
0.112008
A spatially varying two-sample recombinant coalescent, with applications to HIV escape response · NIPS 2008

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

hierarchical bayesian model · 0.1
YearPublicationVenuePosition
2008 A spatially varying two-sample recombinant coalescent, with applications to HIV escape response
abstract
Statistical evolutionary models provide an important mechanism for describing and understanding the escape response of a viral population under a particular therapy. We present a new hierarchical model that incorporates spatially varying mutation and recombination rates at the nucleotide level. It also maintains sep- arate parameters for treatment and control groups, which allows us to estimate treatment effects explicitly. We use the model to investigate the sequence evolu- tion of HIV populations exposed to a recently developed antisense gene therapy, as well as a more conventional drug therapy. The detection of biologically rele- vant and plausible signals in both therapy studies demonstrates the effectiveness of the method.
Alexander Braunstein, Zhi Wei 0001, Shane T. Jensen, Jon D. McAuliffe
NIPS1