Evidence map›Paper›PMID 42182127›Full record

ArticlebioRxiv : the preprint server for biology2026

Lense: Optimizing data preprocessing in single-cell omics using LLMs.

Jingyun Liu, Zhicheng Ji

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. 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
–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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

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

5 · Who and what money

Authors and funding

2 authors.

Jingyun LiuDepartment of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC, USA.
Zhicheng JiDepartment of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC, USA.

Funding

The Duke Senescent Cell Evaluations in Normal Tissues (SCENT) Mapping CenterU54AG075936 · NIA · DUKE UNIVERSITY · PI CHAN, CLIBURN C · 2021 to 2025
$12.7M
Computational methods for in situ spatial transcriptomicsR35GM154865 · NIGMS · DUKE UNIVERSITY · PI Zhicheng Ji · 2024 to 2026
$1.2M
NIA NIH HHS U54 AG075936NIGMS NIH HHS R35 GM154865
6 · The paper itself

Abstract

Data preprocessing is critical for single-cell omics analyses, but default pipelines often underperform on diverse datasets, especially from emerging platforms like spatial transcriptomics. We introduce Lense, a language-model-guided method that automatically selects optimal preprocessing by comparing plots that visualize low-dimensional representations across pipeline variants. Integrated with Seurat, Lense streamlines analysis and improves preprocessing robustness without requiring manual tuning.

Indexed as

Data preprocessingLarge language modelSingle-cell genomicsSpatial genomics

Identifiers

PMID42182127
PMCPMC13192621

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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.