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Novel insights into breast cancer copy number genetic heterogeneity revealed by single-cell genome sequencing

eLife(2020)10.7554/elife.51480Source: DataRank Database

Novel insights into breast cancer copy number genetic heterogeneity revealed by single-cell genome sequencing is a research paper published in eLife (2020). On theSindex it has a DataRank of 0. It has been cited 73 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access73 citations

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (13 grants)Impact (FWCI 3.75)OA: goldTopics (72)IDs (PubMed, PMC, OpenAlex)Annotations (2)SDGs (3)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (25)

Jude Kendall,Konstantin Volyanskyy,Katherine McNamara ORCID,Hilary Cox,Sean D'Italia

Live enrichment

PubMed:32401198 PMC:PMC7220379 OpenAlex:https://openalex.org/W3025790441

NCI NIH HHS

Grant: R01 CA182514

Department of Defense

Grant: W81XWH-11-10747

Susan G. Komen

Grant: IIR13265578

NIH

Grant: P30 -CA008748

Memorial Sloan-Kettering Cancer Center

Grant: Single Cell Sequencing Initiative

NCI NIH HHS

Grant: P30 CA008748

NCI NIH HHS

Grant: P30 CA045508

American Cancer Society

Grant: Research professor

National Institutes of Health

Grant: 2P30CA008748-43

MOUSE GENETICS

Breast Cancer Research Foundation

William C and Joyce C O'Neil Charitable Trust

McFarland Fund

Philips Research North America

FWCI

3.75

Citation Percentile

1.0%

Citation Trend

2020

2021

2022

2023

2024

2025

2026

goldLicense: public-domain

journalhttps://doi.org/10.7554/elife.51480

publisherhttps://doi.org/10.7554/elife.51480

repositoryhttps://pubmed.ncbi.nlm.nih.gov/32401198

repositoryhttps://doaj.org/article/b100cf9df74a4bccbe9405981826f8e4

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/7220379

Fields of Study

Cancer Genomics and DiagnosticsSingle-cell and spatial transcriptomicsGenomic variations and chromosomal abnormalities0301 basic medicine03 medical and health sciences0303 health sciencesBiomarkers, TumorBreast NeoplasmsClinical Trials, Phase II as TopicDNA Copy Number VariationsFemaleGene DosageGenetic HeterogeneityGenetic Predisposition to DiseaseGenomicsHumansPhenotypePrognosisRNA-SeqSingle-Cell AnalysisWhole Genome Sequencing

MeSH Terms

Whole Genome SequencingRNA-SeqBreast NeoplasmsFemaleHumansPhenotypePrognosisBiomarkers, TumorClinical Trials, Phase II as TopicGene DosageGenetic HeterogeneityGenetic Predisposition to DiseaseGenomicsDNA Copy Number VariationsSingle-Cell Analysis

Keywords

Genetic heterogeneityBiologyBreast cancerCopy-number variationGenomicsTumour heterogeneityGeneticsComputational biologyGenomeSomatic evolution in cancerCancerSomatic cellGenePhenotypeHumanCancer BiologyCopy Number AlterationsSingle-cell SequencingDNA Copy Number VariationsQH301-705.5ScienceGene DosageBreast NeoplasmsClinical Trials, Phase II as TopicBiomarkers, TumorHumansGenetic Predisposition to DiseaseRNA-SeqBiology (General)Whole Genome SequencingQRPrognosisMedicineFemaleSingle-Cell Analysis

Sustainable Development Goals

SDG 2: 2. Zero hungerSDG 3: 3. Good healthSDG 0: Good health and well-being

Novel insights into breast cancer copy number genetic heterogeneity revealed by single-cell genome sequencing

FAIR Checklist

Authors (25)

Funding (13 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)