Pilot corpus: NIH-funded biomedical datasets. Any DOI can be scored on demand — network effects sharpen as coverage grows.

Codon and amino acid content are associated with mRNA stability in mammalian cells

PLoS ONE(2020)10.1371/journal.pone.0228730Source: DataRank Database

Codon and amino acid content are associated with mRNA stability in mammalian cells is a research paper published in PLoS ONE (2020). On theSindex it has a DataRank of 0. It has been cited 128 times.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access128 citations

Download PDF

Cite:

Linked data & code

geo gen go interpro doi

DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?

›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (9 grants)Impact (FWCI 4.47)OA: goldTopics (59)Linked Datasets (14)DataCite Reuse (14)IDs (PubMed, PMC, OpenAlex)Annotations (5)SDGs (1)

FAIR Checklist

Context only (not used in score)

Findable (2/2)

Has DOI
Indexed in repositories

Accessible (1/2)

Open Access

Interoperable (2/2)

DataCite relations
Linked datasets

Reusable (0/3)

FAIR checklist signals are shown for context only and do not affect DataRank scoring.

Run a calibrated FAIR evaluation for this paper →

We only score data papers we can read in full — never from an abstract alone.

Authors (6)

Otis Pinkard ORCID,Sophie Martin ORCID,Thomas J. Sweet ORCID,Gavin Hanson ORCID,Jeff Coller ORCID

Live enrichment

PubMed:32053646 PMC:PMC7018022 OpenAlex:https://openalex.org/W3006243445

National Institutes of Health

Grant: GM125086

National Institute of General Medical Sciences

Grant: GM118018

National Institute of General Medical Sciences

Grant: T32GM136570

NIGMS NIH HHS

Grant: R01 GM125086

NIGMS NIH HHS

Grant: T32 GM136503

NIGMS NIH HHS

Grant: R01 GM118018

NIGMS NIH HHS

Grant: T32 GM007250

National Institutes of Health

Grant: 3R01GM125086-02S1

Understanding the interconnection between mRNA turnover and mRNA translation

National Institutes of Health

Grant: 7R01GM118018-04

Determining the influence of codon optimality on mRNA translation and decay

FWCI

4.47

Citation Percentile

1.0%

Citation Trend

2019

2020

2021

2022

2023

2024

2025

2026

goldLicense: cc-by

journalhttps://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0228730&type=printable

publisherhttps://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0228730&type=printable

publisherhttps://dx.plos.org/10.1371/journal.pone.0228730

journalhttps://doi.org/10.1371/journal.pone.0228730

repositoryhttps://pubmed.ncbi.nlm.nih.gov/32053646

Fields of Study

RNA and protein synthesis mechanismsRNA Research and SplicingRNA modifications and cancer0301 basic medicine0303 health sciences03 medical and health sciences

MeSH Terms

Amino AcidsAnimalsCodonCricetulusHalf-LifeCricetinaeHeLa CellsHumansRNA, MessengerRNA, TransferOpen Reading FramesCHO CellsRNA StabilityHela Cells

Keywords

Messenger RNAAmino acidBiologyCodon usage biasNonsense-mediated decayTransfer RNACoding regionP-bodiesGeneRNATranslation (biology)Gene expressionTranslational efficiencyProtein biosynthesisChinese hamster ovary cellGeneticsCell biologyBiochemistryGenomeCell cultureRNA splicingScienceRNA StabilityQRCHO CellsOpen Reading FramesCricetulusRNA, TransferCricetinaeMedicineAnimalsHumansRNA, MessengerAmino AcidsCodonResearch ArticleHalf-LifeHeLa Cells

Sustainable Development Goals

SDG 0: Life in Land

Additional file 10 of Differential regulation of mRNA fate by the human Ccr4-Not complex is driven by coding sequence composition and mRNA localization

10.6084/m9.figshare.16756060.v1figshare

Additional file 10 of Differential regulation of mRNA fate by the human Ccr4-Not complex is driven by coding sequence composition and mRNA localization

10.6084/m9.figshare.16756060figshare

Additional file 11 of Differential regulation of mRNA fate by the human Ccr4-Not complex is driven by coding sequence composition and mRNA localization

10.6084/m9.figshare.16756063.v1figshare

Additional file 11 of Differential regulation of mRNA fate by the human Ccr4-Not complex is driven by coding sequence composition and mRNA localization

10.6084/m9.figshare.16756063figshare

Additional file 1 of Differential regulation of mRNA fate by the human Ccr4-Not complex is driven by coding sequence composition and mRNA localization

10.6084/m9.figshare.16756066.v1figshare

Additional file 1 of Differential regulation of mRNA fate by the human Ccr4-Not complex is driven by coding sequence composition and mRNA localization

10.6084/m9.figshare.16756066figshare

Additional file 9 of Differential regulation of mRNA fate by the human Ccr4-Not complex is driven by coding sequence composition and mRNA localization

10.6084/m9.figshare.16756090.v1figshare

Additional file 9 of Differential regulation of mRNA fate by the human Ccr4-Not complex is driven by coding sequence composition and mRNA localization

10.6084/m9.figshare.16756090figshare

Additional file 2 of Differences in 5'untranslated regions highlight the importance of translational regulation of dosage sensitive genes

10.6084/m9.figshare.25720279.v1figshare

Additional file 2 of Differences in 5'untranslated regions highlight the importance of translational regulation of dosage sensitive genes

10.6084/m9.figshare.25720279figshare

Additional file 3 of Differences in 5'untranslated regions highlight the importance of translational regulation of dosage sensitive genes

10.6084/m9.figshare.26713891.v1figshare

Additional file 3 of Differences in 5'untranslated regions highlight the importance of translational regulation of dosage sensitive genes

10.6084/m9.figshare.26713891figshare

Additional file 1 of Differences in 5'untranslated regions highlight the importance of translational regulation of dosage sensitive genes

10.6084/m9.figshare.25720156figshare

Additional file 1 of Differences in 5'untranslated regions highlight the importance of translational regulation of dosage sensitive genes