Evidence map›Paper›PMID 31680375›Full record

ArticleHuman mutation2020

Matching whole genomes to rare genetic disorders: Identification of potential causative variants using phenotype-weighted knowledge in the CAGI SickKids5 clinical genomes challenge.

Lipika R Pal, Kunal Kundu, Yizhou Yin, John Moult

Abstract read
In one paragraph

Article in Human mutation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. 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

4 authors.

Lipika R PalInstitute for Bioscience and Biotechnology Research, University of Maryland, Rockville, Maryland.ORCID 0000-0002-3390-110X
Kunal KunduInstitute for Bioscience and Biotechnology Research, University of Maryland, Rockville, Maryland.ORCID 0000-0002-4452-4290
Yizhou YinInstitute for Bioscience and Biotechnology Research, University of Maryland, Rockville, Maryland.ORCID 0000-0002-5365-2294
John MoultInstitute for Bioscience and Biotechnology Research, University of Maryland, Rockville, Maryland.ORCID 0000-0002-3012-2282

Funding

Component 2 - Resource ProjectU41HG007346 · NHGRI · UNIVERSITY OF CALIFORNIA BERKELEY · PI BRENNER, STEVEN E · 2015 to 2017
$1.7M
Mechanisms underlying complex trait human diseaseR01GM104436 · NIGMS · UNIV OF MARYLAND, COLLEGE PARK · PI MOULT, JOHN · 2013 to 2016
$1.1M
Molecular impact of mutations in monogenic disease and cancerR01GM120364 · NIGMS · UNIV OF MARYLAND, COLLEGE PARK · PI MOULT, JOHN · 2016 to 2018
$1.1M
Critical Assessment of Genome Interpretation ConferenceR13HG006650 · NHGRI · UNIVERSITY OF CALIFORNIA BERKELEY · PI BRENNER, STEVEN E · 2011 to 2018
$165k
NHGRI NIH HHS R13 HG006650NHGRI NIH HHS U41 HG007346NIGMS NIH HHS R01 GM104436NIGMS NIH HHS R01 GM120364
6 · The paper itself

Abstract

Precise identification of causative variants from whole-genome sequencing data, including both coding and noncoding variants, is challenging. The Critical Assessment of Genome Interpretation 5 SickKids clinical genome challenge provided an opportunity to assess our ability to extract such information. Participants in the challenge were required to match each of the 24 whole-genome sequences to the correct phenotypic profile and to identify the disease class of each genome. These are all rare disease cases that have resisted genetic diagnosis in a state-of-the-art pipeline. The patients have a range of eye, neurological, and connective-tissue disorders. We used a gene-centric approach to address this problem, assigning each gene a multiphenotype-matching score. Mutations in the top-scoring genes for each phenotype profile were ranked on a 6-point scale of pathogenicity probability, resulting in an approximately equal number of top-ranked coding and noncoding candidate variants overall. We were able to assign the correct disease class for 12 cases and the correct genome to a clinical profile for five cases. The challenge assessor found genes in three of these five cases as likely appropriate. In the postsubmission phase, after careful screening of the genes in the correct genome, we identified additional potential diagnostic variants, a high proportion of which are noncoding.

Indexed as

Genetic Predisposition to DiseaseGenome, HumanRare DiseasesAlgorithmsAllelesGenetic Association StudiesGenetic Diseases, InbornGenetic VariationGenome-Wide Association StudyGenomicsGenotypeHumansModels, TheoreticalPhenotypeWhole Genome SequencingWorkflowCAGI5connective-tissue disorderdiagnostic variantseye disorderHuman Phenotype Ontology (HPO)neurological diseaseswhole-genome sequencing data

Identifiers

PMID31680375
PMCPMC7182498

What Socratic holds

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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.