Evidence map›Paper›PMID 36865385›Full record

ArticleFrontiers in genetics2023

iPoLNG-An unsupervised model for the integrative analysis of single-cell multiomics data.

Wenyu Zhang, Zhixiang Lin

Abstract read
In one paragraph

Article in Frontiers in genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Wenyu ZhangDepartment of Statistics, The Chinese University of Hong Kong, Hong Kong, China.
Zhixiang LinDepartment of Statistics, The Chinese University of Hong Kong, Hong Kong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single-cell multiomics technologies, where the transcriptomic and epigenomic profiles are simultaneously measured in the same set of single cells, pose significant challenges for effective integrative analysis. Here, we propose an unsupervised generative model, iPoLNG, for the effective and scalable integration of single-cell multiomics data. iPoLNG reconstructs low-dimensional representations of the cells and features using computationally efficient stochastic variational inference by modelling the discrete counts in single-cell multiomics data with latent factors. The low-dimensional representation of cells enables the identification of distinct cell types, and the feature by factor loading matrices help characterize cell-type specific markers and provide rich biological insights on the functional pathway enrichment analysis. iPoLNG is also able to handle the setting of partial information where certain modality of the cells is missing. Taking advantage of GPU and probabilistic programming, iPoLNG is scalable to large datasets and it takes less than 15 min to implement on datasets with 20,000 cells.

Indexed as

generative modelintegrative analysisprobabilistic non-negative matrix factorizationsingle-cell multi-omics datastochastic variational inferenceunsupervised learning

Identifiers

PMID36865385
PMCPMC9972291

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.