Evidence map›Paper›PMID 29950021›Full record

ArticleBioinformatics (Oxford, England)2018

LONGO: an R package for interactive gene length dependent analysis for neuronal identity.

Matthew J McCoy, Alexander J Paul, Matheus B Victor, Michelle Richner, Harrison W Gabel, Haijun Gong, Andrew S Yoo, Tae-Hyuk Ahn

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. eNeuro · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Article
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  8. Article
  9. Article
  10. Review
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  12. MiR-124 synergism with ELAVL3 enhances target gene expression to promote neuronal maturity.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  13. Article
  14. 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

8 authors.

Matthew J McCoyDepartment of Developmental Biology, Washington University School of Medicine, Saint Louis, MO, USA.
Alexander J PaulProgram in Bioinformatics & Computational Biology, Saint Louis University, Saint Louis, MO, USA.
Matheus B VictorDepartment of Developmental Biology, Washington University School of Medicine, Saint Louis, MO, USA.
Michelle RichnerDepartment of Developmental Biology, Washington University School of Medicine, Saint Louis, MO, USA.
Harrison W GabelDepartment of Neuroscience, Washington University School of Medicine, Saint Louis, MO, USA.
Haijun GongDepartment of Mathematics & Statistics, Saint Louis University, Saint Louis, MO, USA.
Andrew S YooDepartment of Developmental Biology, Washington University School of Medicine, Saint Louis, MO, USA.
Tae-Hyuk AhnProgram in Bioinformatics & Computational Biology, Saint Louis University, Saint Louis, MO, USA.

Funding

MICRORNA AND NEURAL FACTOR-MEDIATED DIRECT REPROGRAMMING OF CELL FATESDP2NS083372 · NINDS · WASHINGTON UNIVERSITY · PI YOO, ANDREW · 2012 to 2017
$2.7M
Training At The Interface of Psychology, Neuroscience, and GeneticsT32GM081739 · NIGMS · WASHINGTON UNIVERSITY · PI BARCH, DEANNA · 2007 to 2016
$2.1M
Modeling Neuronal Aging and Alzheimer's Disease in Human Neurons Directly Converted from FibroblastsRF1AG056296 · NIA · WASHINGTON UNIVERSITY · PI YOO, ANDREW · 2017 to 2017
$1.9M
NIA NIH HHS RF1 AG056296NIGMS NIH HHS T32 GM081739NINDS NIH HHS DP2 NS083372
6 · The paper itself

Abstract

Motivation: Reprogramming somatic cells into neurons holds great promise to model neuronal development and disease. The efficiency and success rate of neuronal reprogramming, however, may vary between different conversion platforms and cell types, thereby necessitating an unbiased, systematic approach to estimate neuronal identity of converted cells. Recent studies have demonstrated that long genes (>100 kb from transcription start to end) are highly enriched in neurons, which provides an opportunity to identify neurons based on the expression of these long genes. Results: We have developed a versatile R package, LONGO, to analyze gene expression based on gene length. We propose a systematic analysis of long gene expression (LGE) with a metric termed the long gene quotient (LQ) that quantifies LGE in RNA-seq or microarray data to validate neuronal identity at the single-cell and population levels. This unique feature of neurons provides an opportunity to utilize measurements of LGE in transcriptome data to quickly and easily distinguish neurons from non-neuronal cells. By combining this conceptual advancement and statistical tool in a user-friendly and interactive software package, we intend to encourage and simplify further investigation into LGE, particularly as it applies to validating and improving neuronal differentiation and reprogramming methodologies. Availability and implementation: LONGO is freely available for download at https://github.com/biohpc/longo. Supplementary information: Supplementary data are available at Bioinformatics online.

Indexed as

Cellular ReprogrammingSoftwareAgedFemaleGene Expression ProfilingHumansMaleMiddle AgedNeuronsOligonucleotide Array Sequence AnalysisSequence Analysis, RNATranscriptome

Identifiers

PMID29950021
PMCPMC6022641

What OpenQuestion holds

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LicenceCC BY-NC
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.