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Supriya Munshaw

dblp:21/7970 · DBLP profile ↗
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1ranked-venue papers
1as first author
0since 2021 · last 2010
—ORCID · unresolved

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

Applied, interdisciplinary, general and emerging computing · 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 2 heaviest of 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › immunoinformatics
b cell repertoire analysis
0.112010
SoDA2: a Hidden Markov Model approach for identification of immunoglobulin rearrangements · Bioinform. 2010
Bioinformatics and computational biology › sequence analysis › sequence modeling
probabilistic sequence modeling
0.112010
SoDA2: a Hidden Markov Model approach for identification of immunoglobulin rearrangements · Bioinform. 2010

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

hidden markov model · 0.1bayesian inference · 0.1
YearPublicationVenuePosition
2010 SoDA2: a Hidden Markov Model approach for identification of immunoglobulin rearrangements
abstract
MOTIVATION: The inference of pre-mutation immunoglobulin (Ig) rearrangements is essential in the study of the antibody repertoires produced in response to infection, in B-cell neoplasms and in autoimmune disease. Often, there are several rearrangements that are nearly equivalent as candidates for a given Ig gene, but have different consequences in an analysis. Our aim in this article is to develop a probabilistic model of the rearrangement process and a Bayesian method for estimating posterior probabilities for the comparison of multiple plausible rearrangements. RESULTS: We have developed SoDA2, which is based on a Hidden Markov Model and used to compute the posterior probabilities of candidate rearrangements and to find those with the highest values among them. We validated the software on a set of simulated data, a set of clonally related sequences, and a group of randomly selected Ig heavy chains from Genbank. In most tests, SoDA2 performed better than other available software for the task. Furthermore, the output format has been redesigned, in part, to facilitate comparison of multiple solutions. AVAILABILITY: SoDA2 is available online at https://hippocrates.duhs.duke.edu/soda. Simulated sequences are available upon request.
Supriya Munshaw, Thomas B. Kepler
Bioinform.1