Evidence map›Paper›PMID 31691385›Full record

ArticleHuman mutation2020

The Clinical Genome and Ancestry Report: An interactive web application for prioritizing clinically implicated variants from genome sequencing data with ancestry composition.

In-Hee Lee, Jose A Negron, Carles Hernandez-Ferrer, William Jefferson Alvarez, Kenneth D Mandl, Sek Won Kong

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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

In-Hee LeeComputational Health Informatics Program, Boston Children's Hospital, Boston, Massachusetts.ORCID 0000-0002-8857-1355
Jose A NegronComputational Health Informatics Program, Boston Children's Hospital, Boston, Massachusetts.ORCID 0000-0003-3454-0104
Carles Hernandez-FerrerComputational Health Informatics Program, Boston Children's Hospital, Boston, Massachusetts.ORCID 0000-0002-8029-7160
William Jefferson AlvarezComputational Health Informatics Program, Boston Children's Hospital, Boston, Massachusetts.
Kenneth D MandlComputational Health Informatics Program, Boston Children's Hospital, Boston, Massachusetts.ORCID 0000-0002-9781-0477
Sek Won KongComputational Health Informatics Program, Boston Children's Hospital, Boston, Massachusetts.ORCID 0000-0003-4877-7567

Funding

Coordinating Center for the Undiagnosed Diseases NetworkU01HG007530 · NHGRI · HARVARD MEDICAL SCHOOL · PI KOHANE, ISAAC S. · 2014 to 2022
$30.2M
Instrumenting the Delivery System for a Genomics Research Information CommonsU01TR002623 · NCATS · BOSTON CHILDREN'S HOSPITAL · PI MANDL, KENNETH D. · 2019 to 2024
$8.6M
Biorepository of iPSC lines from diverse rat strains for regenerative medicine researchR24OD024622 · OD · MCLEAN HOSPITAL · PI KIM, KWANG-SOO, KONG, SEK WON · 2018 to 2021
$3.4M
An environment-wide association study in autism spectrum disorders using novel bioinformatics methods and metabolomics via mass spectrometryR01MH107205 · NIMH · BOSTON CHILDREN'S HOSPITAL · PI KONG, SEK WON · 2015 to 2019
$2.1M
NCATS NIH HHS U01 TR002623NHGRI NIH HHS U01 HG007530NIH HHS R24 OD024622NIMH NIH HHS R01 MH107205
6 · The paper itself

Abstract

Genome sequencing is positioned as a routine clinical work-up for diverse clinical conditions. A commonly used approach to highlight candidate variants with potential clinical implication is to search over locus- and gene-centric knowledge databases. Most web-based applications allow a federated query across diverse databases for a single variant; however, sifting through a large number of genomic variants with combination of filtering criteria is a substantial challenge. Here we describe the Clinical Genome and Ancestry Report (CGAR), an interactive web application developed to follow clinical interpretation workflows by organizing variants into seven categories: (1) reported disease-associated variants, (2) rare- and high-impact variants in putative disease-associated genes, (3) secondary findings that the American College of Medical Genetics and Genomics recommends reporting back to patients, (4) actionable pharmacogenomic variants, (5) focused reports for candidate genes, (6) de novo variant candidates for trio analysis, and (7) germline and somatic variants implicated in cancer risk, diagnosis, treatment and prognosis. For each variant, a comprehensive list of external links to variant-centric and phenotype databases are provided. Furthermore, genotype-derived ancestral composition is used to highlight allele frequencies from a matched population since some disease-associated variants show a wide variation between populations. CGAR is an open-source software and is available at https://tom.tch.harvard.edu/apps/cgar/.

Indexed as

Databases, GeneticGenome, HumanSoftwareWeb BrowserComputational BiologyGenetic Association StudiesGenetic Predisposition to DiseaseGenetic VariationGenomicsHumansMolecular Sequence AnnotationUser-Computer Interfaceancestrycancerclinical interpretationpharmacogenomicsvariant annotationwhole-genome sequencing

Identifiers

PMID31691385
PMCPMC7180092

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.