Author

Tsun-Po Yang

Wellcome Sanger InstituteORCID 0000-0002-9077-4434Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:experimental assay· 1 Assay:long-read sequencing· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Matthew D. C. NevilleiD· 2 shared Peter J. CampbelliD· 2 shared Raheleh RahbariiD· 2 shared Aylwyn ScallyiD· 1 shared Ayrun NessaiD· 1 shared Chenxi ZhouiD· 1 shared Emily MitchelliD· 1 shared Helen V. FirthiD· 1 shared

Activity by Year

2024-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenetics

Matthew D. C. NevilleORCID

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2 papers

Recent·Most cited

GeneticsbioRxivPreprintJul 5, 2024

Insights into non-crossover recombination from long-read sperm sequencing

Regev Schweiger, Sang-Jin Lee, Chenxi Zhou…·Richard Michael Durbin

The paper uses long-read sperm sequencing to analyze non-crossover recombination events, finding variation in recombination rates and distinct mechanisms for non-crossover gene conversions.

11 citations

humanlong-read sequencing

GenomicsbioRxivPreprintApr 3, 2024

Deciphering the role of germline complex de novo structural variations in rare disorders

Hyunchul Jung, Tsun-Po Yang, Susan Walker…·Raheleh Rahbari

This study identifies de novo structural variants in a large cohort of rare disease patients, highlighting their prevalence and potential pathogenicity.

DOI 10.1101/2024.04.03.587925

humanwhole-genome sequencing