Evidence map›Paper›PMID 34280183›Full record

ArticlePLoS biology2021

Assessing the replicability of spatial gene expression using atlas data from the adult mouse brain.

Shaina Lu, Cantin Ortiz, Daniel Fürth, Stephan Fischer, Konstantinos Meletis, Anthony Zador, Jesse Gillis

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 33% of its field
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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. A Review of the Application of Spatial Transcriptomics in Neuroscience.Interdisciplinary sciences, computational life sciences · 2024
    Review
  4. Article
  5. Article
  6. Article
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

7 authors at 2 institutions in 2 countries.

Shaina LuCold Spring Harbor Laboratory, Cold Spring Harbor, New York, United States of America.ORCID 0000-0001-8616-226X
Cantin OrtizDepartment of Neuroscience, Karolinska Institutet, Solna, Sweden.ORCID 0000-0001-9564-0059
Daniel FürthCold Spring Harbor Laboratory, Cold Spring Harbor, New York, United States of America.ORCID 0000-0002-6017-3419
Stephan FischerCold Spring Harbor Laboratory, Cold Spring Harbor, New York, United States of America.ORCID 0000-0002-7034-4103
Konstantinos MeletisDepartment of Neuroscience, Karolinska Institutet, Solna, Sweden.
Anthony ZadorCold Spring Harbor Laboratory, Cold Spring Harbor, New York, United States of America.
Jesse GillisCold Spring Harbor Laboratory, Cold Spring Harbor, New York, United States of America.
Cold Spring Harbor Laboratory · USKarolinska Institutet · SE

Funding

Tool and Technology Development CoreU19MH114821 · NIMH · COLD SPRING HARBOR LABORATORY · PI HUANG, Z JOSH · 2017 to 2021
$64.5M
SYNPLA: A scaleable method for monitoring circuit-specific learning-induced changes in synaptic strengthU01MH109113 · NIMH · COLD SPRING HARBOR LABORATORY · PI MALINOW, ROBERTO, ZADOR, ANTHONY M · 2015 to 2017
$2.9M
High throughput mapping of neuronal circuitry using DNA sequencingRF1MH114132 · NIMH · COLD SPRING HARBOR LABORATORY · PI ZADOR, ANTHONY M · 2017 to 2017
$2.7M
Revealing the transcriptomic basis of neuronal identity through functional meta-analysisR01MH113005 · NIMH · COLD SPRING HARBOR LABORATORY · PI GILLIS, JESSE · 2017 to 2021
$2.4M
High-throughput DNA sequencing method for probing the connectivity of neural circR01NS073129 · NINDS · COLD SPRING HARBOR LABORATORY · PI ZADOR, ANTHONY M · 2010 to 2014
$2.3M
CRCNS: Theory and experiment of neural circuit mapping by DNA sequencingR01DA036913 · NIDA · COLD SPRING HARBOR LABORATORY · PI KOULAKOV, ALEXEI, ZADOR, ANTHONY M · 2013 to 2017
$2.1M
Heuristics to evaluate biomedical and genomic knowledge bases for validityR01LM012736 · NLM · COLD SPRING HARBOR LABORATORY · PI GILLIS, JESSE · 2017 to 2020
$1.9M
NIDA NIH HHS R01 DA036913NIMH NIH HHS R01 MH113005NIMH NIH HHS RF1 MH114132NIMH NIH HHS U01 MH109113NIMH NIH HHS U19 MH114821NINDS NIH HHS R01 NS073129NLM NIH HHS R01 LM012736
6 · The paper itself

Abstract

High-throughput, spatially resolved gene expression techniques are poised to be transformative across biology by overcoming a central limitation in single-cell biology: the lack of information on relationships that organize the cells into the functional groupings characteristic of tissues in complex multicellular organisms. Spatial expression is particularly interesting in the mammalian brain, which has a highly defined structure, strong spatial constraint in its organization, and detailed multimodal phenotypes for cells and ensembles of cells that can be linked to mesoscale properties such as projection patterns, and from there, to circuits generating behavior. However, as with any type of expression data, cross-dataset benchmarking of spatial data is a crucial first step. Here, we assess the replicability, with reference to canonical brain subdivisions, between the Allen Institute's in situ hybridization data from the adult mouse brain (Allen Brain Atlas (ABA)) and a similar dataset collected using spatial transcriptomics (ST). With the advent of tractable spatial techniques, for the first time, we are able to benchmark the Allen Institute's whole-brain, whole-transcriptome spatial expression dataset with a second independent dataset that similarly spans the whole brain and transcriptome. We use regularized linear regression (LASSO), linear regression, and correlation-based feature selection in a supervised learning framework to classify expression samples relative to their assayed location. We show that Allen Reference Atlas labels are classifiable using transcription in both data sets, but that performance is higher in the ABA than in ST. Furthermore, models trained in one dataset and tested in the opposite dataset do not reproduce classification performance bidirectionally. While an identifying expression profile can be found for a given brain area, it does not generalize to the opposite dataset. In general, we found that canonical brain area labels are classifiable in gene expression space within dataset and that our observed performance is not merely reflecting physical distance in the brain. However, we also show that cross-platform classification is not robust. Emerging spatial datasets from the mouse brain will allow further characterization of cross-dataset replicability ultimately providing a valuable reference set for understanding the cell biology of the brain.

Indexed as

Gene Expression ProfilingAnimalsAtlases as TopicBrainDatasets as TopicMiceReproducibility of Results

Identifiers

PMID34280183
PMCPMC8321401
OpenAlexW3185300724

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.