BiologyarXiv

Ranked by formulaVerdict: Notable

Spatially Informed and Direction Sensitive Representation Learning for Spatial Transcriptomics

Cellular states are shaped by both intrinsic gene expression programs and the spatial microenvironment in which cells reside.

By Amirabad, Yalabadi, Moskalev +4

Score████░░░░░░4.4

Key numbers

  • 16x larger than those seen

VerdictWorth a reader's time today.

Read the originalPDF

Abstract

Cellular states are shaped by both intrinsic gene expression programs and the spatial microenvironment in which cells reside. Spatial transcriptomics makes this context measurable, but effective representation learning requires capturing both spatially informative molecular signals and intercellular organization. Existing approaches address these challenges only partially: conventional gene selection can overlook spatially structured signals, while methods for encoding cell-cell relationships often either reduce a cell's microenvironment to proximity alone, discarding direction, or rely on absolute coordinates tied to an arbitrary tissue frame. Consequently, cells with similar neighbor distances but distinct spatial organization may receive overly similar representations, despite experiencing different biological contexts that shape their cellular states. We introduce Tessera, a spatial representation learning framework that addresses both molecular selection and cellular context. Tessera combines spatially informed gene selection with a geometric inductive bias that contextualizes each cell within its local tissue environment. By modeling relative cell-cell relationships, Tessera is translation-invariant while preserving direction, allowing neighboring cells to contribute differently according to their spatial context and cellular state. Across held-out tissues and technologies, Tessera outperforms existing spatial foundation models in representation quality and generalizes zero-shot to contexts up to 16× larger than those seen during training.

Azim Dehghani Amirabad, Ali Khodabandeh Yalabadi, Artem Moskalev, Yun-Ching Chen, Mehdi Pirooznia, Scott Oloff, Rui Liao

The editor's rubric

Heuristic review

Leverage3 / 5
A method or resource many groups across the field will adopt within a year.
24% of this desk’s rubric
Magnitude3 / 5
Large gain: roughly 2x, or a clear new state of the art on a hard, unsaturated problem.
16% of this desk’s rubric
Evidence3 / 5
Solid: multiple benchmarks or cohorts, ablations, fair baselines, released code or data.
20% of this desk’s rubric
Novelty3 / 5
A genuinely new approach to an open problem.
20% of this desk’s rubric
Trajectory2 / 5
Some room to improve with obvious engineering.
10% of this desk’s rubric
Stakes2 / 5
Benefits a professional community (practitioners, clinicians, engineers).
10% of this desk’s rubric

Editor’s rationale

Heuristic triage from title and abstract text only, not a reading of the paper. Cues found: method (we propose); breadth (zero/few-shot); gains (x-fold, outperforms); verification (held-out test).

How the score was computed

rank-2026-10-18

Score████░░░░░░4.4

Score = 10 × (75% × adjusted merit / 10 + 15% × attention + 10% × freshness)

Desks place stronger verdicts first, then use this score to order work within the same verdict.

Merit
5.6 / 10
Weighted rubric, evidence-gated.
Adjusted merit
4.6 / 10
Shrunk toward the desk prior by editor confidence (40%).
Attention
0%
Citations, upvotes, points, mentions.
Freshness
95%
Half-life decay since publication.

No attention signals recorded yet.

The record

  • Reviewed by heuristic-v7 on Oct 21, 2026, 05:48 UTC. Paper type: method.
  • Categories: q-bio.QM, cs.AI
  • TOP, No.6 in the Biology edition of October 21, 2026.