Demonstration venue · read-only. Every page can be browsed; the buttons that would change it are switched off. Create an account to run TaxoReview on your own data. A simulation from public publication records: the people listed were not invited and did not agree to review.
? Tutorial for this page

Sarah J. Parker

dblp:371/1247 · DBLP profile ↗
← Back
1ranked-venue papers
0as first author
1since 2021 · last 2024
—ORCID · unresolved

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

Applied, interdisciplinary, general and emerging computing · 1 · 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
1 paper
Bioinformatics and computational biology · 100%

Topics — the 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › single-cell analysis
cell type composition estimation
0.812024
CAM3.0: determining cell type composition and expression from bulk tissues with fully unsupervised deconvolution · Bioinform. 2024
Bioinformatics and computational biology
deconvolution
0.812024
CAM3.0: determining cell type composition and expression from bulk tissues with fully unsupervised deconvolution · Bioinform. 2024
Bioinformatics and computational biology
gene expression
0.812024
CAM3.0: determining cell type composition and expression from bulk tissues with fully unsupervised deconvolution · Bioinform. 2024

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

radius-fixed clustering · 0.8linear programming · 0.8floating search · 0.8convex analysis of mixtures · 0.8
YearPublicationVenuePosition
2024 CAM3.0: determining cell type composition and expression from bulk tissues with fully unsupervised deconvolution
abstract
MOTIVATION: Complex tissues are dynamic ecosystems consisting of molecularly distinct yet interacting cell types. Computational deconvolution aims to dissect bulk tissue data into cell type compositions and cell-specific expressions. With few exceptions, most existing deconvolution tools exploit supervised approaches requiring various types of references that may be unreliable or even unavailable for specific tissue microenvironments. RESULTS: We previously developed a fully unsupervised deconvolution method-Convex Analysis of Mixtures (CAM), that enables estimation of cell type composition and expression from bulk tissues. We now introduce CAM3.0 tool that improves this framework with three new and highly efficient algorithms, namely, radius-fixed clustering to identify reliable markers, linear programming to detect an initial scatter simplex, and a smart floating search for the optimum latent variable model. The comparative experimental results obtained from both realistic simulations and case studies show that the CAM3.0 tool can help biologists more accurately identify known or novel cell markers, determine cell proportions, and estimate cell-specific expressions, complementing the existing tools particularly when study- or datatype-specific references are unreliable or unavailable. AVAILABILITY AND IMPLEMENTATION: The open-source R Scripts of CAM3.0 is freely available at https://github.com/ChiungTingWu/CAM3/(https://github.com/Bioconductor/Contributions/issues/3205). A user's guide and a vignette are provided.
Chiung-Ting Wu, Dongping Du, Lulu Chen, Rujia Dai, Chunyu Liu 0001, Guoqiang Yu, Saurabh Bhardwaj, Sarah J. Parker, Robert Clarke, David M. Herrington, Yue Joseph Wang
Bioinform.8