Author

SK. Leung

University of Exeter

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genomics· 1

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Assay:bulk RNA-seq· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Assay:long-read sequencing· 1 Organism:mouse· 1

Frequent Co-Authors

Aaron R. JeffriesiD· 1 shared David Andrew CollieriD· 1 shared Eilis J. HannoniD· 1 shared Elizabeth TsengiD· 1 shared Emma Louise DempsteriD· 1 shared Isabel CastanhoiD· 1 shared Jonathan P. DaviesiD· 1 shared Jonathan S. MilliD· 1 shared

Activity by Year

2020-2020 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Aaron R. JeffriesORCID

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1 paper

Recent·Most cited

Full-length transcript sequencing of human and mouse identifies widespread isoform diversity and alternative splicing in the cerebral cortex

Aaron R. Jeffries, SK. Leung, Isabel Castanho, Karen Moore, Jonathan P. Davies, Emma Louise Dempster, Nicholas J. Bray, P. O‘Neill, Elizabeth Tseng, Zeshan Ahmed, David Andrew Collier, Shyam Prabhakar, Leonard C. Schalkwyk, Michael J. Gandal, Eilis J. Hannon, Jonathan S. Mill

This study uses long-read RNA sequencing to analyze isoform diversity in human and mouse cerebral cortex, revealing widespread alternative splicing and novel transcripts.

bioRxiv · Oct 14, 2020 · PreprintGenomics