Evidence map›Paper›PMID 26266814›Full record

ArticlePloS one2015

Efficient Estimation of Mutation Rates during Individual Development by Minimization of Chi-Square.

Shi-Meng Ai, Jian-Jun Gao, Shu-Qun Liu, Yun-Xin Fu

Abstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

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.

Shi-Meng AiLaboratory for Conservation and Utilization of Bioresources, Yunnan University, Kunming, 650091, China; Department of Applied Mathematics, Yunnan Agricultural University, Kunming, 650201, China.
Jian-Jun GaoLaboratory for Conservation and Utilization of Bioresources, Yunnan University, Kunming, 650091, China.
Shu-Qun LiuLaboratory for Conservation and Utilization of Bioresources, Yunnan University, Kunming, 650091, China.
Yun-Xin FuLaboratory for Conservation and Utilization of Bioresources, Yunnan University, Kunming, 650091, China; Human Genetics Center and Division of Biostatistics, School of Public Health, The University of Texas Health Science Center, Houston, Texas, 77030, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutation primarily occurs when cells divide and it is highly desirable to have knowledge of the rate of mutations for each of the cell divisions during individual development. Recently, recessive lethal or nearly lethal mutations which were observed in a large mutation accumulation experiment using Drosophila melanogaster suggested that mutation rates vary significantly during the germline development of male Drosophila melanogaster. The analysis of the data was based on a combination of the maximum likelihood framework with numerical assistance from a newly developed coalescent algorithm. Although powerful, the likelihood based framework is computationally highly demanding which limited the scope of the inference. This paper presents a new estimation approach by minimizing chi-square statistics which is asymptotically consistent with the maximum likelihood method. When only at most one mutation in a family is considered the minimization of chi-square is simplified to a constrained weighted minimum least square method which can be solved easily by optimization theory. The new methods effectively eliminates the computational bottleneck of the likelihood. Reanalysis of the published Drosophila melanogaster mutation data results in similar estimates of mutation rates. The new method is also expected to be applicable to the analysis of mutation data generated by next-generation sequencing technology.

Indexed as

Germ-Line MutationModels, GeneticMutation RateAnimalsDrosophila melanogasterMaleSpermatogenesis

Identifiers

PMID26266814
PMCPMC4534375

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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.