Evidence map›Paper›PMID 26708336›Full record

ArticleBioinformatics (Oxford, England)2016

rCGH: a comprehensive array-based genomic profile platform for precision medicine.

Frederic Commo, Justin Guinney, Charles Ferté, Brian Bot, Celine Lefebvre, Jean-Charles Soria, Fabrice André

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2016. 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.

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  11. T-cell bispecific antibodies in node-positive breast cancer: novel therapeutic avenue for MHC class I loss variants.Annals of oncology : official journal of the European Society for Medical Oncology · 2019
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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

7 authors.

Frederic CommoINSERM U981, Gustave Roussy, University Paris-Sud, Villejuif 94805, France, Sage Bionetworks, Seattle, WA 98109, USA and.
Justin GuinneySage Bionetworks, Seattle, WA 98109, USA and.
Charles FertéINSERM U981, Gustave Roussy, University Paris-Sud, Villejuif 94805, France, Sage Bionetworks, Seattle, WA 98109, USA and.
Brian BotSage Bionetworks, Seattle, WA 98109, USA and.
Celine LefebvreINSERM U981, Gustave Roussy, University Paris-Sud, Villejuif 94805, France.
Jean-Charles SoriaINSERM U981, Gustave Roussy, University Paris-Sud, Villejuif 94805, France, Department of Medical Oncology, Gustave Roussy, Villejuif 94805, France.
Fabrice AndréINSERM U981, Gustave Roussy, University Paris-Sud, Villejuif 94805, France, Department of Medical Oncology, Gustave Roussy, Villejuif 94805, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledWe present rCGH, a comprehensive array-based comparative genomic hybridization analysis workflow, integrating computational improvements and functionalities specifically designed for precision medicine. rCGH supports the major microarray platforms, ensures a full traceability and facilitates profiles interpretation and decision-making through sharable interactive visualizations. AVAILABILITY AND IMPLEMENTATION: The rCGH R package is available on bioconductor (under Artistic-2.0). The aCGH-viewer is available at https://fredcommo.shinyapps.io/aCGH_viewer, and the application implementation is freely available for installation at https://github.com/fredcommo/aCGH_viewer CONTACT: frederic.commo@gustaveroussy.fr SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

Comparative Genomic HybridizationGenomicsPrecision MedicineHumansSoftware

Identifiers

PMID26708336
PMCPMC4848396

What OpenQuestion holds

Textmetadata
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.