Evidence map›Paper›PMID 31268618›Full record

ArticleHuman mutation2019

What went wrong with variant effect predictor performance for the PCM1 challenge.

Maximilian Miller, Yanran Wang, Yana Bromberg

Abstract read
In one paragraph

Article in Human mutation, 2019. 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
–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

9 citing papers in PubMed.

  1. Article
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  5. Review
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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

3 authors.

Maximilian MillerDepartment of Biochemistry and Microbiology, Rutgers University, New Brunswick, New Jersey.ORCID 0000-0002-1335-9499
Yanran WangDepartment of Biochemistry and Microbiology, Rutgers University, New Brunswick, New Jersey.
Yana BrombergDepartment of Biochemistry and Microbiology, Rutgers University, New Brunswick, New Jersey.ORCID 0000-0002-8351-0844

Funding

The NINDS Human Cell and Data Repository (U24 renewal)U24NS095914 · NINDS · RUTGERS, THE STATE UNIV OF N.J. · PI Azadeh Jadali, JAMES A KNOWLES · 2015 to 2026
$15.9M
1/7 Collaborative Genomic Studies of Tourette Disorder.R01MH115958 · NIMH · RUTGERS, THE STATE UNIV OF N.J. · PI HEIMAN, GARY A., TISCHFIELD, JAY ARNOLD · 2018 to 2023
$6.8M
Component 2 - Resource ProjectU41HG007346 · NHGRI · UNIVERSITY OF CALIFORNIA BERKELEY · PI BRENNER, STEVEN E · 2015 to 2017
$1.7M
AVA,Dx: Analysis of Variation for Association with DiseaseU01GM115486 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI BROMBERG, YANA · 2015 to 2018
$1.2M
AVA,Dx: Analysis of Variation for Association with DiseaseR01GM115486 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI BROMBERG, YANA · 2019 to 2019
$306k
Critical Assessment of Genome Interpretation ConferenceR13HG006650 · NHGRI · UNIVERSITY OF CALIFORNIA BERKELEY · PI BRENNER, STEVEN E · 2011 to 2018
$165k
Health Services and Delivery Research Programme NIH R01 MH115958 01NHGRI NIH HHS R13 HG006650NHGRI NIH HHS U41 HG007346NIGMS NIH HHS R01 GM115486NIGMS NIH HHS U01 GM115486NIH Clinical Center NIH U01 GM115486NIH R01 MH115958NIH R13 HG006650NIH U01 GM115486NIH U41 HG007346NIMH NIH HHS R01 MH115958NINDS NIH HHS U24 NS095914
6 · The paper itself

Abstract

The recent years have seen a drastic increase in the amount of available genomic sequences. Alongside this explosion, hundreds of computational tools were developed to assess the impact of observed genetic variation. Critical Assessment of Genome Interpretation (CAGI) provides a platform to evaluate the performance of these tools in experimentally relevant contexts. In the CAGI-5 challenge assessing the 38 missense variants affecting the human Pericentriolar material 1 protein (PCM1), our SNAP-based submission was the top performer, although it did worse than expected from other evaluations. Here, we compare the CAGI-5 submissions, and 24 additional commonly used variant effect predictors, to analyze the reasons for this observation. We identified per residue conservation, structural, and functional PCM1 characteristics, which may be responsible. As expected, predictors had a hard time distinguishing effect variants in nonconserved positions. They were also better able to call effect variants in a structurally rich region than in a less-structured one; in the latter, they more often correctly identified benign than effect variants. Curiously, most of the protein was predicted to be functionally robust to mutation-a feature that likely makes it a harder problem for generalized variant effect predictors.

Indexed as

Mutation, MissenseAlgorithmsAutoantigensCell Cycle ProteinsComputational BiologyDatabases, GeneticGenetic Predisposition to DiseaseHumansAutoantigensCell Cycle ProteinsPCM1 protein, humanCAGImissense mutationPCM1protein sequence position typesvariant effect prediction

Identifiers

PMID31268618
PMCPMC6744297

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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.