Evidence map›Paper›PMID 30022114›Full record

ArticleNature genetics2018

Author Correction: Quantification of subclonal selection in cancer from bulk sequencing data.

Marc J Williams, Benjamin Werner, Timon Heide, Christina Curtis, Chris P Barnes, Andrea Sottoriva, Trevor A Graham

Abstract readPublished Erratum
PubMed Publisher
In one paragraph

Article in Nature genetics, 2018. 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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Marc J WilliamsEvolution and Cancer Laboratory, Barts Cancer Institute, Queen Mary University of London, London, UK.ORCID http://orcid.org/0000-0001-5524-4174
Benjamin WernerEvolutionary Genomics & Modelling Lab, Centre for Evolution and Cancer, Institute of Cancer Research, London, UK.
Timon HeideEvolutionary Genomics & Modelling Lab, Centre for Evolution and Cancer, Institute of Cancer Research, London, UK.ORCID http://orcid.org/0000-0002-1386-7469
Christina CurtisDepartments of Medicine and Genetics, Stanford University School of Medicine, Stanford, CA, USA.ORCID http://orcid.org/0000-0003-0166-3802
Chris P BarnesDepartment of Cell and Developmental Biology, University College London, London, UK. christopher.barnes@ucl.ac.uk.ORCID http://orcid.org/0000-0002-9459-1395
Andrea SottorivaEvolutionary Genomics & Modelling Lab, Centre for Evolution and Cancer, Institute of Cancer Research, London, UK. andrea.sottoriva@icr.ac.uk.ORCID http://orcid.org/0000-0001-6709-9533
Trevor A GrahamEvolution and Cancer Laboratory, Barts Cancer Institute, Queen Mary University of London, London, UK. t.graham@qmul.ac.uk.ORCID http://orcid.org/0000-0001-9582-1597

Funding

Cancer Research UK 19771Wellcome Trust 202778/Z/16/Z
6 · The paper itself

Abstract

In the version of this article originally published, in the "Theoretical framework of subclonal selection" section of the main text, ref. 11 instead of ref. 19 should have been cited at the end of the phrase "Our previously presented frequentist approach to detect subclonal selection from bulk sequencing data involves an R

Identifiers

PMID30022114

What OpenQuestion holds

Textmetadata
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.