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Long-read sequencing for molecular diagnostics in constitutional disorders

<p>These are the alignment files (.bam) for specific gene regions (TRIOBP for Patient 1 and STRC for Patient 2) from PacBio long-read sequencing. These patients were referred to genetic testing for hearing loss and received an inconclusive result from the standard of care testing. Long-read sequencing was performed to infer phase without parental samples and resolve the diagnostic dilemma. This is part of the publication submitted to Human Mutation (Conlin LK et al.,&nbsp;Long-read sequencing for molecular diagnostics in constitutional genetic disorders, Human Mutation, Submitted).</p>

ShareScore

8/100

Overall dataset sharing score

Score breakdown

These five areas show where the dataset supports — or may limit — practical reuse.

Stewardship
4
Harmonization
4
Access
0
Reuse readiness
0
Engagement
0