Author

Shih‐Feng Tsai

National Health Research InstitutesORCID 0000-0002-2538-4130Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 1 Organism:human· 1 Assay:long-read sequencing· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Chen‐Chi WuiD· 1 shared Cheng‐Yu TsaiiD· 1 shared Chuan‐Jen HsuiD· 1 shared Jacob Shujui HsuiD· 1 shared Ming‐Yu Lo· 1 shared Pei‐Hsuan LiniD· 1 shared Pei‐Lung CheniD· 1 shared Yu‐Ting ChiangiD· 1 shared

Activity by Year

2024-2024 · peak 1/yr

Co-Author Collaboration Network

9 top collaborators · 36 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenetic & Genomic Medicine

Chen‐Chi WuORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintNov 5, 2024

Comprehensive genetic analysis of STRC variants in hereditary hearing impairment using long-read sequencing

Cheng‐Yu Tsai, Yue-Sheng Lu, Yu‐Ting Chiang…·Chen‐Chi Wu

This study uses long-read sequencing to identify STRC variants in patients with hereditary hearing impairment, finding 11% diagnostic yield and highlighting LRS's ability to detect complex variants missed by conventional NGS.

1 citation

humanlong-read sequencing

𝕏 PostBluesky