Evidence map›Paper›PMID 32024824›Full record

ArticleNature communications2020

Estimating growth patterns and driver effects in tumor evolution from individual samples.

Leonidas Salichos, William Meyerson, Jonathan Warrell, Mark Gerstein

Abstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
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  3. Review
  4. Article
  5. Article
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  11. Review
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  15. Article
  16. New Insights into Therapy-Induced Progression of Cancer.International journal of molecular sciences · 2020
    Review
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

4 authors.

Leonidas SalichosProgram in Computational Biology and Bioinformatics, Yale University, New Haven, CT, 06520, USA.ORCID http://orcid.org/0000-0003-0228-6885
William MeyersonProgram in Computational Biology and Bioinformatics, Yale University, New Haven, CT, 06520, USA.
Jonathan WarrellProgram in Computational Biology and Bioinformatics, Yale University, New Haven, CT, 06520, USA.ORCID http://orcid.org/0000-0002-1323-4602
Mark GersteinProgram in Computational Biology and Bioinformatics, Yale University, New Haven, CT, 06520, USA. pi@gersteinlab.org.ORCID http://orcid.org/0000-0002-9746-3719

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007205 · NIGMS · YALE UNIVERSITY · PI KAZMIERCZAK, BARBARA I · 1985 to 2019
$42.9M
Prioritizing rare variants associated with cancer using non-coding annotationR01HG008126 · NHGRI · YALE UNIVERSITY · PI GERSTEIN, MARK BENDER · 2016 to 2018
$2.4M
NHGRI NIH HHS R01 HG008126NIGMS NIH HHS T32 GM007205U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01 HG 008126
6 · The paper itself

Abstract

Tumors accumulate thousands of mutations, and sequencing them has given rise to methods for finding cancer drivers via mutational recurrence. However, these methods require large cohorts and underperform for low recurrence. Recently, ultra-deep sequencing has enabled accurate measurement of VAFs (variant-allele frequencies) for mutations, allowing the determination of evolutionary trajectories. Here, based solely on the VAF spectrum for an individual sample, we report on a method that identifies drivers and quantifies tumor growth. Drivers introduce perturbations into the spectrum, and our method uses the frequency of hitchhiking mutations preceding a driver to measure this. As validation, we use simulation models and 993 tumors from the Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium with previously identified drivers. Then we apply our method to an ultra-deep sequenced acute myeloid leukemia (AML) tumor and identify known cancer genes and additional driver candidates. In summary, our framework presents opportunities for personalized driver diagnosis using sequencing data from a single individual.

Indexed as

Genes, Tumor SuppressorModels, GeneticMutationAlgorithmsGene FrequencyHigh-Throughput Nucleotide SequencingHumansLeukemia, Myeloid, AcuteMutation, MissenseMutation RateNeoplasmsOncogenesPrecision MedicineStochastic Processes

Identifiers

PMID32024824
PMCPMC7002450

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.