Evidence map›Paper›PMID 30252889›Full record

ArticlePloS one2018

Spatial statistical tools for genome-wide mutation cluster detection under a microarray probe sampling system.

Bin Luo, Alanna K Edge, Cornelia Tolg, Eva A Turley, C B Dean, Kathleen A Hill, R J Kulperger

Open access · goldAbstract read
In one paragraph

Article in PloS one, 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, top 91% of its field
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, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 3 institutions in 1 country.

Bin LuoDepartment of Statistical and Actuarial Sciences, Western University, London, Ontario, Canada.ORCID 0000-0002-0608-9793
Alanna K EdgeDepartment of Biology, Western University, London, Ontario, Canada.
Cornelia TolgLondon Regional Cancer Program, Lawson Health Research Institute, London, Ontario, Canada.
Eva A TurleyLondon Regional Cancer Program, Lawson Health Research Institute, London, Ontario, Canada.
C B DeanDepartment of Statistics and Actuarial Science, University of Waterloo, Waterloo, Ontario, Canada.
Kathleen A HillDepartment of Biology, Western University, London, Ontario, Canada.
R J KulpergerDepartment of Statistical and Actuarial Sciences, Western University, London, Ontario, Canada.
Western University · CALawson Health Research Institute · CAUniversity of Waterloo · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutation cluster analysis is critical for understanding certain mutational mechanisms relevant to genetic disease, diversity, and evolution. Yet, whole genome sequencing for detection of mutation clusters is prohibitive with high cost for most organisms and population surveys. Single nucleotide polymorphism (SNP) genotyping arrays, like the Mouse Diversity Genotyping Array, offer an alternative low-cost, screening for mutations at hundreds of thousands of loci across the genome using experimental designs that permit capture of de novo mutations in any tissue. Formal statistical tools for genome-wide detection of mutation clusters under a microarray probe sampling system are yet to be established. A challenge in the development of statistical methods is that microarray detection of mutation clusters is constrained to select SNP loci captured by probes on the array. This paper develops a Monte Carlo framework for cluster testing and assesses test statistics for capturing potential deviations from spatial randomness which are motivated by, and incorporate, the array design. While null distributions of the test statistics are established under spatial randomness via the homogeneous Poisson process, power performance of the test statistics is evaluated under postulated types of Neyman-Scott clustering processes through Monte Carlo simulation. A new statistic is developed and recommended as a screening tool for mutation cluster detection. The statistic is demonstrated to be excellent in terms of its robustness and power performance, and useful for cluster analysis in settings of missing data. The test statistic can also be generalized to any one dimensional system where every site is observed, such as DNA sequencing data. The paper illustrates how the informal graphical tools for detecting clusters may be misleading. The statistic is used for finding clusters of putative SNP differences in a mixture of different mouse genetic backgrounds and clusters of de novo SNP differences arising between tissues with development and carcinogenesis.

Indexed as

GenomeOligonucleotide Array Sequence AnalysisStatistics as TopicAlgorithmsAnimalsChromosomes, MammalianCluster AnalysisComputer SimulationDNA ProbesGenetic VariationGenotypeMiceMutationPolymorphism, Single NucleotideDNA Probes

Identifiers

PMID30252889
PMCPMC6155535
OpenAlexW2893214649

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.