Evidence mapPaperPMID 38714942Full record

ArticleBMC genomic data2024

Dataset including whole blood gene expression profiles and matched leukocyte counts with utility for benchmarking cellular deconvolution pipelines.

Grant C O'Connell

Abstract read
In one paragraph

Article in BMC genomic data, 2024. 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

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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

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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

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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

1 author.

Grant C O'ConnellMolecular Biomarker Core, Case Western Reserve University, Cleveland, OH, USA. grant.oconnell@case.edu.

Funding

Investigation of brain-originating circRNAs as targets in blood-based stroke triage diagnosticsR01NS129876 · NINDS · CASE WESTERN RESERVE UNIVERSITY · 2023 to 2025
$1.2M
NINDS NIH HHS R01 NS129876NINDS NIH HHS R01NS129876NINR NIH HHS R21 NR019337NINR NIH HHS R21NR019337
6 · The paper itself

Abstract

objectivesCellular deconvolution is a valuable computational process that can infer the cellular composition of heterogeneous tissue samples from bulk RNA-sequencing data. Benchmark testing is a crucial step in the development and evaluation of new cellular deconvolution algorithms, and also plays a key role in the process of building and optimizing deconvolution pipelines for specific experimental applications. However, few in vivo benchmarking datasets exist, particularly for whole blood, which is the single most profiled human tissue. Here, we describe a unique dataset containing whole blood gene expression profiles and matched circulating leukocyte counts from a large cohort of human donors with utility for benchmarking cellular deconvolution pipelines. DATA DESCRIPTION: To produce this dataset, venous whole blood was sampled from 138 total donors recruited at an academic medical center. Genome-wide expression profiling was subsequently performed via next-generation RNA sequencing, and white blood cell differentials were collected in parallel using flow cytometry. The resultant final dataset contains donor-level expression data for over 45,000 protein coding and non-protein coding genes, as well as matched neutrophil, lymphocyte, monocyte, and eosinophil counts.

Indexed as

BenchmarkingAlgorithmsGene Expression ProfilingHigh-Throughput Nucleotide SequencingHumansLeukocyte CountLeukocytesSequence Analysis, RNATranscriptomeBenchmarkingBloodDeconvolutionMethodsReference datasetRNA-seqWhite blood cells

Identifiers

PMID38714942
PMCPMC11077736

What Socratic holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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 Socratic graph.