Evidence map›Paper›PMID 41292735›Full record

ArticlebioRxiv : the preprint server for biology2025

Fast Optimization of Robust Transcriptomics Embeddings using Probabilistic Inference Autoencoder Networks for multi-Omics.

Ning Wang, David Turner, Hannah Feinberg, Victor Eduardo Nieto Caballero, Dan Yuan, Nathaniel Scott, Christopher Cardenas, Michael DeBerardine, Shu Dan, Lakme Caceres and 5 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

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

15 authors.

Ning WangPrinceton Neuroscience Institute (PNI).ORCID 0000-0003-3073-7911
David TurnerPrinceton Neuroscience Institute (PNI).
Hannah FeinbergPrinceton Neuroscience Institute (PNI).
Victor Eduardo Nieto CaballeroPrinceton Neuroscience Institute (PNI).
Dan YuanAllen Institute for Brain Science (AIBS).
Nathaniel ScottPrinceton Neuroscience Institute (PNI).
Christopher CardenasPrinceton Neuroscience Institute (PNI).
Michael DeBerardinePrinceton Neuroscience Institute (PNI).ORCID 0000-0002-5220-0341
Shu DanPrinceton Neuroscience Institute (PNI).ORCID 0009-0002-8442-5999
Lakme CaceresPrinceton Neuroscience Institute (PNI).ORCID 0000-0002-2019-0505
Jessica SchembriPrinceton Neuroscience Institute (PNI).
Zizhen YaoAllen Institute for Brain Science (AIBS).ORCID 0000-0002-9361-5607
Changkyu LeeAllen Institute for Brain Science (AIBS).ORCID 0000-0001-6146-0404
Jonathan W PillowPrinceton Neuroscience Institute (PNI).ORCID 0000-0002-3638-8831
Fenna M KrienenPrinceton Neuroscience Institute (PNI).ORCID 0000-0002-1400-6820

Funding

Functionally guided adult whole brain cell atlas in human and NHPUM1MH130981 · NIMH · ALLEN INSTITUTE · PI Ed Lein, Hongkui Zeng · 2022 to 2026
$91.9M
NRSA Training Grant in Quantitative NeuroscienceT32MH065214 · NIMH · PRINCETON UNIVERSITY · PI Nathaniel Douglass Daw, KENNETH A NORMAN · 2002 to 2026
$7.9M
Genomic recording systems to reveal evolutionary modifications in primate neocortexDP2MH140136 · NIMH · PRINCETON UNIVERSITY · PI KRIENEN, FENNA MARIE · 2024 to 2024
$1.4M
NIMH NIH HHS DP2 MH140136NIMH NIH HHS T32 MH065214NIMH NIH HHS UM1 MH130981
6 · The paper itself

Abstract

Advances in single-cell genomics technologies enable the routine acquisition of atlases with millions of cells. These datasets often include multiple covariates, such as donors, sequencing platforms, developmental timepoints, and species, which provide new opportunities for discovery and new challenges. To mitigate unwanted sources of variation, dataset integration is the starting point for most analyses. However, existing methods struggle with integrating large complex datasets. To address these limitations, we developed PIANO, a variational autoencoder framework that uses a negative binomial generalized linear model for stronger batch correction, and code compilation for ten times faster training than existing tools. We first demonstrate performant integration compared to commonly used methods on single-species datasets. We then show PIANO enables superior analyses of multiple atlases, solving challenging integration tasks across sequencing platforms, development, and species, while simultaneously preserving desired biological signals. Our contributions include a novel, high-performance integration method and recommendations for integration applications.

Indexed as

Cross-species atlasesDeep LearningIntegrationMethods DevelopmentMulti-omicsSingle cell RNA sequencingSpatial TranscriptomicsTranscriptomics

Identifiers

PMID41292735
PMCPMC12642614

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.