Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
0numbers the graph read from it
0cells of the map it votes in
2citing 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.
Yuval KlugerComputational Biology & Biomedical Informatics Program, Yale University, New Haven, CT, USA. yuval.kluger@yale.edu.ORCID http://orcid.org/0000-0002-3035-071X
Funding
Yale SPORE in Skin CancerP50CA121974 · NCI · YALE UNIVERSITY · PI MARCUS W BOSENBERG, Harriet M. Kluger · 2006 to 2026
$43.9M
The Y-SCORCH Data Generation Center at Yale for Single-Cell Opioid Responses in the Context of HIVUM1DA051410 · NIDA · YALE UNIVERSITY · PI GERSTEIN, MARK BENDER, KLUGER, YUVAL · 2020 to 2025
$15.3M
M-SCORCH: Methamphetamine use disorder data generation center for Single Cell Opioid Responses in the Context of HIVU01DA053628 · NIDA · YALE UNIVERSITY · PI HO, YA-CHI, SESTAN, NENAD · 2021 to 2025
$9.5M
Yale TMC for Cellular Senescence in Lymphoid OrgansU54AG076043 · NIA · YALE UNIVERSITY · PI FAN, RONG, HALENE, STEPHANIE · 2021 to 2025
$7.0M
Yale Murine-TMC on Immune Cell Senescence Derived InflammationU54AG079759 · NIA · YALE UNIVERSITY · PI DIXIT, VISHWA DEEP, MONTGOMERY, RUTH R · 2022 to 2025
$6.5M
Delineating spatiotemporal dynamics of hair follicle dermal niche specification at the single-cell levelR01AR076420 · NIAMS · YALE UNIVERSITY · PI MYUNG, PEGGY S · 2020 to 2024
$1.8M
Evaluating the role of opioid medication assisted therapies in HIV-1 Persistence for persons living with HIV and opioid use disordersR33DA047037 · NIDA · YALE UNIVERSITY · PI HO, YA-CHI, KLUGER, YUVAL · 2021 to 2022
$1.7M
EFFICIENT METHODS FOR CALIBRATION, CLUSTERING, VISUALIZATION AND IMPUTATION OF LARGE scRNA-seq DATAR01GM131642 · NIGMS · YALE UNIVERSITY · PI KLUGER, YUVAL · 2019 to 2022
$1.6M
NCI NIH HHS P50 CA121974NIAMS NIH HHS R01 AR076420NIA NIH HHS U54 AG076043NIA NIH HHS U54 AG079759NIDA NIH HHS R33 DA047037NIDA NIH HHS U01 DA053628NIDA NIH HHS UM1 DA051410NIGMS NIH HHS R01 GM131642NSF | Directorate for Mathematical & Physical Sciences | Division of Mathematical Sciences (DMS) DMS-2007040NSF | Directorate for Mathematical & Physical Sciences | Division of Mathematical Sciences (DMS) DMS-2237842Simons Foundation MPS-MODL-00814643U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) P50CA121974U.S. Department of Health & Human Services | NIH | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) R01AR076420U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R01GM131642U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) U54AG076043U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) U54AG079759U.S. Department of Health & Human Services | NIH | National Institute on Drug Abuse (NIDA) R33DA047037U.S. Department of Health & Human Services | NIH | National Institute on Drug Abuse (NIDA) U01DA053628U.S. Department of Health & Human Services | NIH | National Institute on Drug Abuse (NIDA) UM1PA051410
6 · The paper itself
Abstract
Identifying accurate cell markers in single-cell RNA-seq data is crucial for understanding cellular diversity and function. Localized Marker Detector (LMD) is a novel tool to identify "localized genes"-genes exclusively expressed in groups of highly similar cells-thereby characterizing cellular diversity in a multi-resolution and fine-grained manner. LMD constructs a cell-cell affinity graph, diffuses the gene expression value across the cell graph, and assigns a score to each gene based on its diffusion dynamics. LMD's candidate markers can be grouped into functional gene modules, which accurately reflect cell types, subtypes, and other sources of variation such as cell cycle status. We apply LMD to mouse bone marrow and hair follicle dermal condensate datasets, where it facilitates cross-sample comparisons by identifying shared and sample-specific gene signatures and novel cell populations, without requiring batch effect correction or integration. We also assess the performance of LMD across ten single-cell RNA sequencing datasets, compare it to eight existing methods with similar objectives, and find that LMD outperforms the other methods evaluated.
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.
Cluster-independent multiscale marker identification in single-cell RNA-seq data using localized marker detector (LMD). · full record | OpenQuestion