Whole Genome Trio Sequencing as a Standard Routine Test in Patients With Rare Diseases - "GENOME FIRST APPROACH"

University Hospital Tuebingen

Status: Completed

Conditions: Genetic Predisposition; Rare Diseases

Treatments: Genetic: WGS-Diagnostic

Study type: Interventional

Funder types: Other

Identifiers

NCT03954652

WG-Trio01

Details and patient eligibility

About

The GENOME FIRST APPROACH project will enroll patients (n = 450) and their healthy parents with unclear molecular cause of the disease, suspected genetic cause of the disease and the healthy parents of those affected for trio analysis (N in total 1350).

Full description

In the GENOME FIRST APPROACH (monocentric, prospective, open-label diagnostic) project, patients with molecularly undiagnosed diseases will diagnostically be analyzed by Whole Genome Sequencing (WGS)-trio analysis. The following questions will be leading the project:

Primary:

• Efficacy of WGS trio analysis in different clinical indications

Secondary:

• Systematically benchmark WGS analysis to detect genetic variations compared to WES and single nucleotide polymorphism (SNP) array analysis,
• Expand the analysis from coding single-nucleotide variants (SNVs) to regulatory mutations, structural variants (SVs), and low complexity regions,
• Validate the efficacy of clinical genome trio sequencing in a routine diagnostic setting,
• Analyse whether 42x coverage has the potential to discover mosaicism as disease causing mechanism,
• Further develop algorithms for integrative analyses of Trio-WGS data with Ribonucleic acid- sequencing (RNA-seq),
• Identify de novo alterations and novel disease mechanisms,
• Gain fundamental new insights into disease mechanisms and cellular biology,
• Combine WGS with further Omics methods to improve genetic diagnostics of future rare disease patients, and
• Explore overall financial costs and time to report conclusive data to the patients of the Trio-WGS approach compared to traditional multistep diagnostic approaches using single-gene, panel, whole-exome sequencing (WES) and chromosomal microarray (CMA) (SNP array, array-based comparative genomic hybridization (arrayCGH)) analysis.

In addition, healthy parents of the subjects will be included in the project to perform parent-child (trio) analyzes.

Enrollment: 1,350 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• Unclear molecular cause of the disease
• Suspected genetic cause of the disease
• Healthy parents of those affected for trio analysis Cohort 1: IQ < 70 with and without malformations, syndromic and non-syndromic Cohort 2: Retinitis pigmentosa, achromatopsy, Bardet-Biedl syndrome, Usher syndrome, congenital stationary night blindness, LCA, macula degeneration, rod/ cone dystrophies, opticus atrophy Cohort 3: Rare paediatric solid cancers as melanoma, carcinoma of the gastrointestinal tract, tumours of the salivary gland and pancreatic tumors in children.

Exclusion criteria

Cohort 1: Toxic causes (drugs, infections) Cohort 2: patients with non-genetic forms of blindness Cohort 3: adult cancer, blood cancer

• Missing informed consent of the patient/ legal guardian
• Missing samples of both parents
• Previous WES or panel analysis-

Trial design

Primary purpose: Basic Science

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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1,350 participants in 3 patient groups

Cohort 1: Intellectual disability

Other group

Description:

Genetic: WGS Diagnostic Blood take for genetic diagnostic.

Treatment:

Genetic: WGS-Diagnostic

Cohort 2 Retinal diseases

Other group

Description:

Genetic: WGS Diagnostic Blood take for genetic diagnostic.

Treatment:

Genetic: WGS-Diagnostic

Cohort 3: Rare tumors in childhood

Other group

Description:

Genetic: WGS Diagnostic Blood take for genetic diagnostic.

Treatment:

Genetic: WGS-Diagnostic