Evidence map›Paper›PMID 27355347›Full record

ArticlePLoS computational biology2016

Rare Variants Association Analysis in Large-Scale Sequencing Studies at the Single Locus Level.

Xinge Jessie Jeng, Zhongyin John Daye, Wenbin Lu, Jung-Ying Tzeng

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.8field-weighted citation impact, top 13% 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

5 citing papers in PubMed, 15 citations in OpenAlex.

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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 at 2 institutions in 2 countries.

Xinge Jessie JengDepartment of Statistics, North Carolina State University, Raleigh, North Carolina, United States of America.
Zhongyin John DayeEpidemiology and Biostatistics, University of Arizona, Tucson, Arizona, United States of America.
Wenbin LuDepartment of Statistics, North Carolina State University, Raleigh, North Carolina, United States of America.
Jung-Ying TzengDepartment of Statistics, North Carolina State University, Raleigh, North Carolina, United States of America.
North Carolina State University · USUniversity of Arizona · US

Funding

Statistical Methods for Cancer Clinical TrialsP01CA142538 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KOSOROK, MICHAEL R · 2010 to 2019
$21.3M
Powerful and Adaptive Statistical Methods for Sequencing StudiesR03HG008642 · NHGRI · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI JENG, XINGE JESSIE · 2016 to 2017
$152k
NCI NIH HHS P01 CA142538NHGRI NIH HHS R03 HG008642
6 · The paper itself

Abstract

Genetic association analyses of rare variants in next-generation sequencing (NGS) studies are fundamentally challenging due to the presence of a very large number of candidate variants at extremely low minor allele frequencies. Recent developments often focus on pooling multiple variants to provide association analysis at the gene instead of the locus level. Nonetheless, pinpointing individual variants is a critical goal for genomic researches as such information can facilitate the precise delineation of molecular mechanisms and functions of genetic factors on diseases. Due to the extreme rarity of mutations and high-dimensionality, significances of causal variants cannot easily stand out from those of noncausal ones. Consequently, standard false-positive control procedures, such as the Bonferroni and false discovery rate (FDR), are often impractical to apply, as a majority of the causal variants can only be identified along with a few but unknown number of noncausal variants. To provide informative analysis of individual variants in large-scale sequencing studies, we propose the Adaptive False-Negative Control (AFNC) procedure that can include a large proportion of causal variants with high confidence by introducing a novel statistical inquiry to determine those variants that can be confidently dispatched as noncausal. The AFNC provides a general framework that can accommodate for a variety of models and significance tests. The procedure is computationally efficient and can adapt to the underlying proportion of causal variants and quality of significance rankings. Extensive simulation studies across a plethora of scenarios demonstrate that the AFNC is advantageous for identifying individual rare variants, whereas the Bonferroni and FDR are exceedingly over-conservative for rare variants association studies. In the analyses of the CoLaus dataset, AFNC has identified individual variants most responsible for gene-level significances. Moreover, single-variant results using the AFNC have been successfully applied to infer related genes with annotation information.

Indexed as

Genetic Association StudiesGenomicsHigh-Throughput Nucleotide SequencingCardiovascular DiseasesComputer SimulationDatabases, FactualDrug Delivery SystemsGene FrequencyGenetic Predisposition to DiseaseHumansModels, Genetic

Identifiers

PMID27355347
PMCPMC4927097
OpenAlexW2469769396

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LicenceCC BY
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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.