Semi-automated genomic newborn screening highlights complexities in reporting

Newborn screening programs are instrumental in the early detection of treatable conditions in the first days of life. By integrating genomic approaches, there is potential to expand the range of conditions included in these programs. As part of a research study, NewbornsInSA, we validated a genomic newborn screening workflow. Analysis of whole-genome sequencing data was restricted to a virtual panel of 613 genes, selected through engagement with local clinical teams. We assessed the workflow's performance using retrospective samples with known variant status. To reduce manual curation time, bioinformatics scripts were developed to auto-classify cases into those with no findings and those requiring manual review. We report on early findings from applying this workflow to a prospectively recruited cohort in which five reportable findings have been made to date. We discuss reporting challenges encountered in genes associated with multiple conditions, with incomplete penetrance, or variants associated with only mild phenotypes.

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Publication Details

Journal
npj Genomic Medicine
Published
2026-02-10
DOI
https://doi.org/10.1038/s41525-026-00553-4
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
0.00

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article

Semi-automated genomic newborn screening highlights complexities in reporting

Khoa Lam, Rosalie Kenyon, Lucy T. Anastasi, Tracy Merlin et al.
npj Genomic Medicine
Genomics and Rare Diseases
article

Semi-automated genomic newborn screening highlights complexities in reporting

Khoa Lam, Rosalie Kenyon, Lucy T. Anastasi, Tracy Merlin, Ben R. Saxon, Shashikanth Marri, Tomas Rozek, Kirsty Stallard, Dominik C. Kaczorowski, Lucas Dejong, Ayesha Chowdhury, Jinghua Feng, Abhi Kulkarni, Sunita De Sousa, Hung Nguyen, Carol Wai-Kwan Siu, Jovanka King, Nicholas W. G. Smith, Alex Ashenden, Enzo Ranieri, Christopher Barnett, Hamish S. Scott
article en

Abstract

Newborn screening programs are instrumental in the early detection of treatable conditions in the first days of life. By integrating genomic approaches, there is potential to expand the range of conditions included in these programs. As part of a research study, NewbornsInSA, we validated a genomic newborn screening workflow. Analysis of whole-genome sequencing data was restricted to a virtual panel of 613 genes, selected through engagement with local clinical teams. We assessed the workflow's performance using retrospective samples with known variant status. To reduce manual curation time, bioinformatics scripts were developed to auto-classify cases into those with no findings and those requiring manual review. We report on early findings from applying this workflow to a prospectively recruited cohort in which five reportable findings have been made to date. We discuss reporting challenges encountered in genes associated with multiple conditions, with incomplete penetrance, or variants associated with only mild phenotypes.

npj Genomic MedicineVol. 11(1)
South Australia Pathology (AU), Royal Adelaide Hospital (AU), Women's and Children's Hospital (AU), Children's Hospital at Westmead (AU), Women's and Children's Health Network (AU), Centre for Cancer Biology (AU), The University of Adelaide (AU)
Australian Government
Openalex Percentile: Top 58%
Genomics and Rare Diseases
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