Evidence map›Paper›PMID 35098354›Full record

ArticleHuman genetics2022

Evaluating the relevance of sequence conservation in the prediction of pathogenic missense variants.

Emidio Capriotti, Piero Fariselli

Abstract read
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In one paragraph

Article in Human genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Integrative analysis of KCNQ1 variants reveals molecular mechanisms of type 1 long QT syndrome pathogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Review
  7. Pathogenicity of de novo CACNA1D CaEuropean journal of human genetics : EJHG · 2024
    Article
  8. Article
  9. Resources and tools for rare disease variant interpretation.Frontiers in molecular biosciences · 2023
    Review
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

2 authors at 2 institutions in 2 countries.

Emidio CapriottiBioFolD Unit, Department of Pharmacy and Biotechnology (FaBiT), University of Bologna, Via F. Selmi 3, 40126, Bologna, Italy. emidio.capriotti@unibo.it.ORCID http://orcid.org/0000-0002-2323-0963
Piero FariselliDepartment of Medical Sciences, University of Torino, Via Santena 19, 10126, Turin, Italy. piero.fariselli@unito.it.
Department of Medical Sciences · BYUniversity of Bologna · IT

Funding

Ministero dell'Istruzione, dell'Università e della Ricerca PRIN201744NR8S
6 · The paper itself

Abstract

Evolutionary information is the primary tool for detecting functional conservation in nucleic acid and protein. This information has been extensively used to predict structure, interactions and functions in macromolecules. Pathogenicity prediction models rely on multiple sequence alignment information at different levels. However, most accurate genome-wide variant deleteriousness ranking algorithms consider different features to assess the impact of variants. Here, we analyze three different ways of extracting evolutionary information from sequence alignments in the context of pathogenicity predictions at DNA and protein levels. We showed that protein sequence-based information is slightly more informative in the annotation of Clinvar missense variants than those obtained at the DNA level. Furthermore, to achieve the performance of state-of-the-art methods, such as CADD and REVEL, the conservation of reference and variant, encoded as frequencies of reference/alternate alleles or wild-type/mutant residues, should be included. Our results on a large set of missense variants show that a basic method based on three input features derived from the protein sequence profile performs similarly to the CADD algorithm which uses hundreds of genomic features. As expected, our method results in ~ 3% lower area under the receiver-operating characteristic curve (AUC). When compared with an ensemble-based algorithm (REVEL). Nevertheless, the combination of predictions of multiple methods can help to identify more reliable predictions. These observations indicate that for missense variants, evolutionary information, when properly encoded, plays the primary role in ranking pathogenicity.

Indexed as

Computational BiologyNucleic AcidsAlgorithmsAmino Acid SequenceHumansMutation, MissenseSequence AlignmentNucleic Acids

Identifiers

PMID35098354
OpenAlexW4220702430

What Socratic holds

Textmetadata
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 Socratic graph.