Evidence map›Paper›PMID 29186385›Full record

ArticleBioinformatics (Oxford, England)2018

Identifying simultaneous rearrangements in cancer genomes.

Layla Oesper, Simone Dantas, Benjamin J Raphael

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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Chromothripsis.Methods in molecular biology (Clifton, N.J.) · 2025
    Review
  2. A new algebraic approach to genome rearrangement models.Journal of mathematical biology · 2022
    Article
  3. 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

3 authors.

Layla OesperDepartment of Computer Science, Carleton College, Northfield, MN, USA.
Simone DantasInstitute of Mathematics and Statistics, Fluminense Federal University, Niterói, Rio de Janeiro, Brazil.
Benjamin J RaphaelDepartment of Computer Science, Princeton University, Princeton, NJ, USA.

Funding

Pathway and Network Integration of Cancer Genomics and Clinical DataU24CA211000 · NCI · PRINCETON UNIVERSITY · PI RAPHAEL, BENJAMIN, YEH, JEN JEN · 2016 to 2020
$1.7M
Computational Characterization of Genetic HeterogeneityR01HG007069 · NHGRI · PRINCETON UNIVERSITY · PI RAPHAEL, BENJAMIN · 2013 to 2015
$1.1M
NCI NIH HHS U24 CA211000NHGRI NIH HHS R01 HG007069
6 · The paper itself

Abstract

motivationThe traditional view of cancer evolution states that a cancer genome accumulates a sequential ordering of mutations over a long period of time. However, in recent years it has been suggested that a cancer genome may instead undergo a one-time catastrophic event, such as chromothripsis, where a large number of mutations instead occur simultaneously. A number of potential signatures of chromothripsis have been proposed. In this work, we provide a rigorous formulation and analysis of the 'ability to walk the derivative chromosome' signature originally proposed by Korbel and Campbell. In particular, we show that this signature, as originally envisioned, may not always be present in a chromothripsis genome and we provide a precise quantification of under what circumstances it would be present. We also propose a variation on this signature, the H/T alternating fraction, which allows us to overcome some of the limitations of the original signature.

resultsWe apply our measure to both simulated data and a previously analyzed real cancer dataset and find that the H/T alternating fraction may provide useful signal for distinguishing genomes having acquired mutations simultaneously from those acquired in a sequential fashion. AVAILABILITY AND IMPLEMENTATION: An implementation of the H/T alternating fraction is available at https://bitbucket.org/oesperlab/ht-altfrac. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Identifiers

PMID29186385
PMCPMC5860217

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.