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Haotian Teng

dblp:313/5149 · DBLP profile ↗
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1ranked-venue papers
1as first author
1since 2021 · last 2022
0000-0003-0337-8722ORCID · reported

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

Applied, interdisciplinary, general and emerging computing · 1 · 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
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 › single-cell analysis › cell clustering
cell type clustering
0.612022
Clustering spatial transcriptomics data · Bioinform. 2022
Bioinformatics and computational biology › transcriptomics
spatial transcriptomics
0.612022
Clustering spatial transcriptomics data · Bioinform. 2022

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

probabilistic modeling · 0.6inference algorithms · 0.6
YearPublicationVenuePosition
2022 Clustering spatial transcriptomics data
abstract
MOTIVATION: Recent advancements in fluorescence in situ hybridization (FISH) techniques enable them to concurrently obtain information on the location and gene expression of single cells. A key question in the initial analysis of such spatial transcriptomics data is the assignment of cell types. To date, most studies used methods that only rely on the expression levels of the genes in each cell for such assignments. To fully utilize the data and to improve the ability to identify novel sub-types, we developed a new method, FICT, which combines both expression and neighborhood information when assigning cell types. RESULTS: FICT optimizes a probabilistic function that we formalize and for which we provide learning and inference algorithms. We used FICT to analyze both simulated and several real spatial transcriptomics data. As we show, FICT can accurately identify cell types and sub-types, improving on expression only methods and other methods proposed for clustering spatial transcriptomics data. Some of the spatial sub-types identified by FICT provide novel hypotheses about the new functions for excitatory and inhibitory neurons. AVAILABILITY AND IMPLEMENTATION: FICT is available at: https://github.com/haotianteng/FICT. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Haotian Teng, Ziv Bar-Joseph
Bioinform.1