Evidence map›Paper›PMID 23895164›Full record

ArticleGenome biology2013

THetA: inferring intra-tumor heterogeneity from high-throughput DNA sequencing data.

Layla Oesper, Ahmad Mahmoody, Benjamin J Raphael

Abstract read
In one paragraph

Article in Genome biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 133 papers.

0numbers the graph read from it
0cells of the map it votes in
133citing 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

133 citing papers in PubMed.

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73 more citing papers are in PubMed but not listed here.

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 Oesper
Ahmad Mahmoody
Benjamin J Raphael

Funding

Computational Approaches for Structural Variation Studies in GenomesR01HG005690 · NHGRI · BROWN UNIVERSITY · PI RAPHAEL, BENJAMIN · 2011 to 2015
$2.4M
NHGRI NIH HHS R01 HG005690NHGRI NIH HHS R01 HG5690
6 · The paper itself

Abstract

Tumor samples are typically heterogeneous, containing admixture by normal, non-cancerous cells and one or more subpopulations of cancerous cells. Whole-genome sequencing of a tumor sample yields reads from this mixture, but does not directly reveal the cell of origin for each read. We introduce THetA (Tumor Heterogeneity Analysis), an algorithm that infers the most likely collection of genomes and their proportions in a sample, for the case where copy number aberrations distinguish subpopulations. THetA successfully estimates normal admixture and recovers clonal and subclonal copy number aberrations in real and simulated sequencing data. THetA is available at http://compbio.cs.brown.edu/software/.

Indexed as

Genetic HeterogeneitySoftwareAlgorithmsBreast NeoplasmsComputer SimulationFemaleGenome, HumanHigh-Throughput Nucleotide SequencingHumansLikelihood FunctionsStatistics as Topic

Identifiers

PMID23895164
PMCPMC4054893

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.