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Validation of Optical Genome Mapping for the Identification of Constitutional Genomic Variants in a Postnatal Cohort

Recruiting
Conditions
Developmental Disability
Fragile X Syndrome
Intellectual Disability
Facioscapulohumeral Muscular Dystrophy 1
Autism Spectrum Disorder
Congenital Anomaly
Interventions
Other: Standard of care genetic testing group
Registration Number
NCT05295277
Lead Sponsor
Bionano Genomics
Brief Summary

The purpose of this research use only (RUO) study is to detect genomic structural variants (SVs) in human DNA by Optical Genome Mapping (OGM) using the Bionano Genomics Saphyr system. SVs are a type of genetic alternation that includes deletions, duplications, and both balanced and unbalanced rearrangements (ex: inversions or translocations), as well as specific repeat expansions and contractions. The results of OGM analysis will be compared to prior clinical genetic test results to determine how OGM compares to current standard of care (SOC) clinical test methods such as chromosomal microarray analysis (CMA), karyotyping, Southern blot analysis, polymerase chain reaction (PCR), fluorescence in situ hybridization (FISH), and/or next generation sequencing (NGS), etc.

Detailed Description

Optical genome mapping (OGM) is an emerging next-generation cytogenomic tool that enables a comprehensive analysis of structural variants (SVs) in the genome. OGM, in its current iteration, is performed on the Saphyr system, which is developed and marketed by Bionano Genomics (San Diego, CA). OGM employs imaging of ultra-long DNA molecules (\>150 kbp) that are labeled at a unique 6 base-pair sequence motif (CTTAAG) that occurs throughout the genome. The images of the labeled DNA molecules are used to generate a de novo assembly that can be compared to a reference genome to identify all classes of SVs, such as deletions, duplications, balanced/ unbalanced genomic rearrangements (insertions, inversions, and translocations), and repeat array expansions/contractions). In addition, a separate coverage-based algorithm enables the detection of genome-wide copy number analysis (similar to CMA), and the absence of heterozygosity (AOH) analysis. In the same assay, a concurrent or stepwise data analysis pipeline allows for sizing pathogenic CGG repeat expansions (consistent with fragile X syndrome) as well as D4Z4 repeat contractions which are consistent with facioscapulohumeral muscular dystrophy type 1 (FSHD1). Recently, in several studies, OGM has demonstrated excellent concordance with standard-of-care testing. Importantly, the OGM workflow can provide results within three-five days.

The aim of this double-blinded, multi-site, retrospective, observational, Institutional Review Board (IRB)-approved study is to evaluate the concordance of structural variant detection by OGM compared to standard of care tests (such as CMA, karyotyping, Southern blot analysis, PCR, FISH, and/or NGS, etc.), in a large cohort containing a variety of SVs including aneuploidies, intragenic and contiguous deletions, duplications, balanced and unbalanced translocations, inversions, isochromosomes, ring chromosomes, repeat expansions, repeat contractions, and more. This study is also designed to assess the sensitivity, specificity, and reproducibility of OGM analysis conducted at multiple sites, by numerous operators, and on different Saphyr instruments. Consensus testing and interpretation protocols were developed and implemented at all sites.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
1000
Inclusion Criteria
  1. Individual with a genomic aberration identified by CMA, karyotyping, Southern blot analysis, PCR, FISH, and/or NGS or other standard of care (SOC) genetic testing technology whose clinical test results are available to compare with results from OGM.
  2. Patients with prior negative SOC genetic testing results whose results are available to compare with results from OGM.
Exclusion Criteria
  1. Any individual who opted-out of research at the testing laboratory.
  2. An individual whose genetic test contains the following variants: pathogenic sequence variants, abnormalities involving acrocentric p-arms and centromeres, below 20% for mosaicism, and tetraploidy.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Standard of care genetic testing groupStandard of care genetic testing groupIndividuals with genomic test results from a standard of care (SOC) test (such as CMA, karyotyping, Southern blot analysis, PCR, FISH, and/or NGS, etc.) will be enrolled in the study to compare the SOC result to results from optical genome mapping.
Primary Outcome Measures
NameTimeMethod
Sensitivity/Concordance and specificity of OGM with standard of care testing for detection of structural variants.Through study completion, an average of 1 year

OGM results are evaluated against the standard of care test and concordance (sensitivity and specificity) will be determined.

Secondary Outcome Measures
NameTimeMethod
Reproducibility and identification of structural variants beyond the limit of detection of standard of care methods.Through study completion, an average of 1 year

Inter-site as well as inter and intra-run variability of OGM will be assessed by reproducibility studies.

Trial Locations

Locations (8)

Columbia University Irving Medical Center

🇺🇸

New York, New York, United States

DNA Microarray CGH Laboratory, Department of Pathology, University of Rochester Medical Center

🇺🇸

W. Henrietta, New York, United States

Greenwood Genetic Center

🇺🇸

Greenwood, South Carolina, United States

Praxis Genomics

🇺🇸

Atlanta, Georgia, United States

University of Iowa Hospitals & Clinics, Molecular Pathology

🇺🇸

Iowa City, Iowa, United States

Augusta University Research Institute

🇺🇸

Augusta, Georgia, United States

Lineagen (A Bionano Genomics Company)

🇺🇸

Salt Lake City, Utah, United States

Medical College of Wisconsin

🇺🇸

Milwaukee, Wisconsin, United States

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