Evidence map›Paper›PMID 37387155›Full record

ArticleBioinformatics (Oxford, England)2023

Robust reconstruction of single-cell RNA-seq data with iterative gene weight updates.

Yueqi Sheng, Boaz Barak, Mor Nitzan

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Yueqi ShengSchool of Engineering and Applied Sciences, Harvard University, Boston, MA 02134, United States.
Boaz BarakSchool of Engineering and Applied Sciences, Harvard University, Boston, MA 02134, United States.
Mor NitzanSchool of Computer Science and Engineering, Racah Institute of Physics, Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem 9190401, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationSingle-cell RNA-sequencing technologies have greatly enhanced our understanding of heterogeneous cell populations and underlying regulatory processes. However, structural (spatial or temporal) relations between cells are lost during cell dissociation. These relations are crucial for identifying associated biological processes. Many existing tissue-reconstruction algorithms use prior information about subsets of genes that are informative with respect to the structure or process to be reconstructed. When such information is not available, and in the general case when the input genes code for multiple processes, including being susceptible to noise, biological reconstruction is often computationally challenging.

resultsWe propose an algorithm that iteratively identifies manifold-informative genes using existing reconstruction algorithms for single-cell RNA-seq data as subroutine. We show that our algorithm improves the quality of tissue reconstruction for diverse synthetic and real scRNA-seq data, including data from the mammalian intestinal epithelium and liver lobules. AVAILABILITY AND IMPLEMENTATION: The code and data for benchmarking are available at github.com/syq2012/iterative_weight_update_for_reconstruction.

Indexed as

AlgorithmsSingle-Cell Gene Expression AnalysisAnimalsMammals

Identifiers

PMID37387155
PMCPMC10311330

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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.