Author

Tansel Ersavas

Garvan Institute of Medical Research

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

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Genomics· 1

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Research Focus:benchmarking· 1 Approach:deep learning· 1 Assay:long-read sequencing· 1 Approach:statistical model· 1

Frequent Co-Authors

Eva Maria NovoaiD· 1 shared Huanle LiuiD· 1 shared James M. FergusoniD· 1 shared Kirston BartoniD· 1 shared Lilly Bojarski· 1 shared Martin A. SmithiD· 1 shared Morghan C. LucasiD· 1 shared Oguzhan BegikiD· 1 shared

Activity by Year

2020-2020 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 28 mutual co-author links

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1 shared paperGenomics

Eva Maria NovoaORCID

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1 paper

Recent·Most cited

Barcoding and demultiplexing Oxford Nanopore native RNA sequencing reads with deep residual learning

Martin A. Smith, Tansel Ersavas, James M. Ferguson, Huanle Liu, Morghan C. Lucas, Oguzhan Begik, Lilly Bojarski, Kirston Barton, Eva Maria Novoa

This paper introduces a deep learning method for barcoding and demultiplexing direct RNA sequencing reads without base-calling or additional library steps, achieving high specificity and read demultiplexing rates.

Genome Research · Sep 1, 2020Peer-reviewedGenomics