Evidence map›Paper›PMID 35453737›Full record

ArticleBiology2022

AmazonForest: In Silico Metaprediction of Pathogenic Variants.

Helber Gonzales Almeida Palheta, Wanderson Gonçalves Gonçalves, Leonardo Miranda Brito, Arthur Ribeiro Dos Santos, Marlon Dos Reis Matsumoto, Ândrea Ribeiro-Dos-Santos, Gilderlanio Santana de Araújo

Abstract read
In one paragraph

Article in Biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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.

Helber Gonzales Almeida PalhetaLaboratory of Human and Medical Genetics, Graduate Program of Genetics and Molecular Biology, Institute of Biological Sciences, Federal University of Pará, Belém 66075-110, Brazil.ORCID 0000-0003-0916-6616
Wanderson Gonçalves GonçalvesLaboratory of Human and Medical Genetics, Graduate Program of Genetics and Molecular Biology, Institute of Biological Sciences, Federal University of Pará, Belém 66075-110, Brazil.ORCID 0000-0003-0918-1728
Leonardo Miranda BritoLaboratory of Human and Medical Genetics, Graduate Program of Genetics and Molecular Biology, Institute of Biological Sciences, Federal University of Pará, Belém 66075-110, Brazil.ORCID 0000-0002-0598-5115
Arthur Ribeiro Dos SantosLaboratory of Human and Medical Genetics, Graduate Program of Genetics and Molecular Biology, Institute of Biological Sciences, Federal University of Pará, Belém 66075-110, Brazil.ORCID 0000-0002-6697-4698
Marlon Dos Reis MatsumotoLaboratory of Human and Medical Genetics, Graduate Program of Genetics and Molecular Biology, Institute of Biological Sciences, Federal University of Pará, Belém 66075-110, Brazil.ORCID 0000-0001-8479-6912
Ândrea Ribeiro-Dos-SantosLaboratory of Human and Medical Genetics, Graduate Program of Genetics and Molecular Biology, Institute of Biological Sciences, Federal University of Pará, Belém 66075-110, Brazil.ORCID 0000-0001-7001-1483
Gilderlanio Santana de AraújoLaboratory of Human and Medical Genetics, Graduate Program of Genetics and Molecular Biology, Institute of Biological Sciences, Federal University of Pará, Belém 66075-110, Brazil.ORCID 0000-0001-9199-9419

Funding

Amazon Research Foundation No. BJT - 2021/658671
6 · The paper itself

Abstract

ClinVar is a web platform that stores ∼789,000 genetic associations with complex diseases. A partial set of these cataloged genetic associations has challenged clinicians and geneticists, often leading to conflicting interpretations or uncertain clinical impact significance. In this study, we addressed the (re)classification of genetic variants by AmazonForest, which is a random-forest-based pathogenicity metaprediction model that works by combining functional impact data from eight prediction tools. We evaluated the performance of representation learning algorithms such as autoencoders to propose a better strategy. All metaprediction models were trained with ClinVar data, and genetic variants were annotated with eight functional impact predictors cataloged with SnpEff/SnpSift. AmazonForest implements the best random forest model with a one hot data-encoding strategy, which shows an Area Under ROC Curve of ≥0.93. AmazonForest was employed for pathogenicity prediction of a set of ∼101,000 genetic variants of uncertain significance or conflict of interpretation. Our findings revealed ∼24,000 variants with high pathogenic probability (RFprob≥0.9). In addition, we show results for Alzheimer's Disease as a demonstration of its application in clinical interpretation of genetic variants in complex diseases. Lastly, AmazonForest is available as a web tool and R object that can be loaded to perform pathogenicity predictions.

Indexed as

clinical impactencoding datafunctional impactgenetic variantsmetapredictionrandom forestrepresentation learning

Identifiers

PMID35453737
PMCPMC9024711

What OpenQuestion holds

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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.