Evidence map›Paper›PMID 31235655›Full record

ArticleGenome research2019

Genetic variant pathogenicity prediction trained using disease-specific clinical sequencing data sets.

Perry Evans, Chao Wu, Amanda Lindy, Dianalee A McKnight, Matthew Lebo, Mahdi Sarmady, Ahmad N Abou Tayoun

Abstract readEvaluation Study
In one paragraph

Article in Genome research, 2019. 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.

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  11. Statistical models of the genetic etiology of congenital heart disease.Current opinion in genetics & development · 2022
    Review
  12. Evaluating the impact of in silico predictors on clinical variant classification.Genetics in medicine : official journal of the American College of Medical Genetics · 2022
    Article
  13. Article
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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

7 authors.

Perry EvansDepartment of Biomedical and Health Informatics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.
Chao WuDivision of Genomic Diagnostics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.
Amanda LindyGeneDx, Gaithersburg, Maryland 20877, USA.
Dianalee A McKnightGeneDx, Gaithersburg, Maryland 20877, USA.
Matthew LeboLaboratory for Molecular Medicine, Partners HealthCare Personalized Medicine, Cambridge, Massachusetts 02139, USA.
Mahdi SarmadyDivision of Genomic Diagnostics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.
Ahmad N Abou TayounDivision of Genomic Diagnostics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.ORCID 0000-0002-9134-1673

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent advances in DNA sequencing have expanded our understanding of the molecular basis of genetic disorders and increased the utilization of clinical genomic tests. Given the paucity of evidence to accurately classify each variant and the difficulty of experimentally evaluating its clinical significance, a large number of variants generated by clinical tests are reported as variants of unknown clinical significance. Population-scale variant databases can improve clinical interpretation. Specifically, pathogenicity prediction for novel missense variants can use features describing regional variant constraint. Constrained genomic regions are those that have an unusually low variant count in the general population. Computational methods have been introduced to capture these regions and incorporate them into pathogenicity classifiers, but these methods have yet to be compared on an independent clinical variant data set. Here, we introduce one variant data set derived from clinical sequencing panels and use it to compare the ability of different genomic constraint metrics to determine missense variant pathogenicity. This data set is compiled from 17,071 patients surveyed with clinical genomic sequencing for cardiomyopathy, epilepsy, or RASopathies. We further use this data set to demonstrate the necessity of disease-specific classifiers and to train PathoPredictor, a disease-specific ensemble classifier of pathogenicity based on regional constraint and variant-level features. PathoPredictor achieves an average precision >90% for variants from all 99 tested disease genes while approaching 100% accuracy for some genes. The accumulation of larger clinical variant training data sets can significantly enhance their performance in a disease- and gene-specific manner.

Indexed as

Datasets as TopicGenetic VariationCardiomyopathiesEpilepsyHumansMutation, Missenseras Proteinsras Proteins

Identifiers

PMID31235655
PMCPMC6633260

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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.