Evidence map›Paper›PMID 42605801›Full record

ArticleNucleic acids research2026

Binary-SPA: a reference-free method for cell annotation in high-resolution spatial transcriptomics.

Honghao Bi, Wenjie Cai, Pan Wang, Kehan Ren, Inci Aydemir, Ermin Li, Johanna Melo-Cardenas, Matthew J Schipma, Ching Man Wai, Peng Ji

Abstract read
In one paragraph

Article in Nucleic acids research, 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

10 authors.

Honghao BiDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, United States.
Wenjie CaiDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, United States.
Pan WangDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, United States.
Kehan RenDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, United States.ORCID 0000-0002-4409-7145
Inci AydemirDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, United States.
Ermin LiDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, United States.
Johanna Melo-CardenasDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, United States.
Matthew J SchipmaDepartment of Biochemistry and Molecular Genetics, Northwestern University, Chicago, IL 60611, United States.
Ching Man WaiDepartment of Biochemistry and Molecular Genetics, Northwestern University, Chicago, IL 60611, United States.
Peng JiDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, United States.ORCID 0000-0002-8849-3625

Funding

Targeting gasdermin D to treat myelodysplastic syndromesR01HL169507 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Peng Ji · 2023 to 2026
$2.1M
The roles of mDia2 in hematopoietic stem and progenitor cell engraftment and migrationR01HL148012 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI JI, PENG · 2020 to 2023
$2.1M
The roles of mDia2 in membrane remodeling and organelle clearance during reticulocyte formationR01DK124220 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI JI, PENG · 2020 to 2024
$2.0M
The role of Pleckstrin-2 as a functional node in myeloid proliferationR01HL150729 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI JI, PENG · 2020 to 2023
$2.0M
Functional roles of DDX41 in the homeostasis of G quadruplexes in erythropoiesisR01DK138205 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Peng Ji · 2024 to 2026
$1.4M
Deciphering erythroblastic islands in mice and humans during development and stressR01DK142814 · NIDDK · NORTHWESTERN UNIVERSITY · PI Peng Ji · 2026 to 2026
$680k
The functional role of DDX41 in myelodysplastic syndromesF32HL170648 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BI, HONGHAO · 2023 to 2025
$249k
F32 Ruth L. Kirschstein Postdoctoral Individual National Research Service Award F32-HL170648NHLBI NIH HHS F32 HL170648NHLBI NIH HHS R01 HL148012NHLBI NIH HHS R01-HL148012NHLBI NIH HHS R01 HL150729NHLBI NIH HHS R01-HL150729NHLBI NIH HHS R01 HL169507NHLBI NIH HHS R01-HL169507NIDDK NIH HHS R01 DK124220NIDDK NIH HHS R01-DK124220NIDDK NIH HHS R01 DK138205NIDDK NIH HHS R01-DK138205NIDDK NIH HHS R01 DK142814NIDDK NIH HHS R01-DK142814
6 · The paper itself

Abstract

Accurate cell annotation is a primary challenge in spatial transcriptomics (ST). Current approaches primarily rely on label transfer from single-cell RNA sequencing (scRNA-seq) reference or marker-based clustering. While these methods are widely used, they have critical limitations. Label transfer approaches depend on the availability of a well-matched scRNA-seq reference. Marker-based annotation methods often suffer from accuracy and limited coverage. To address these challenges, we developed Binary-SPA (Binary Self-referenced Projection Annotation), a computational framework for cell-type annotation of high-resolution ST. Binary-SPA performs annotation in two stages. First, a binary classification step identifies high-confidence cells using predefined marker sets. These confidently annotated cells are then used as an internal reference for anchor-based label transfer in the second stage. Binary-SPA consistently outperforms conventional marker-based methods and matches or exceeds label-transfer methods across diverse spatial platforms, tissue types, and preservation protocols-without requiring matched reference data. Unlike label transfer methods that decline without same-tissue references, Binary-SPA eliminates external data dependencies entirely while maintaining high accuracy at high annotation coverage. Binary-SPA demonstrates robust performance in challenging specimens such as bone marrow biopsies, and validation against matched COMET protein expression data confirmed strong concordance between transcriptomic- and protein-based cell identities. Binary-SPA thus provides a robust, reference-free solution for ST annotation with broad applicability to research and clinical specimens.

Indexed as

Molecular Sequence AnnotationSoftwareTranscriptomeAlgorithmsAnimalsGene Expression ProfilingHumansSequence Analysis, RNASingle-Cell AnalysisSingle-Cell Gene Expression AnalysisSpatial Transcriptomics

Identifiers

PMID42605801
PMCPMC13478750

What OpenQuestion holds

Textmetadata
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.