Long-read sequencing for molecular diagnostics in constitutional disorders
收藏NIAID Data Ecosystem2026-03-13 收录
下载链接:
https://zenodo.org/record/6668854
下载链接
链接失效反馈官方服务:
资源简介:
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., Long-read sequencing for molecular diagnostics in constitutional genetic disorders, Human Mutation, Submitted).
创建时间:
2022-06-20



