Author

Andrew Brown

Centre for Human GeneticsORCID 0000-0002-4951-3056Unclaimed ORCID profile · follow to get notified of new preprints

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Andrew Brown2 papers · University of British Columbia

Biology Disciplines

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Bioinformatics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Antony J. CutleriD· 1 shared Barbara XellaiD· 1 shared Craig H. CortoniD· 1 shared David BuckiD· 1 shared David Flores Santa Cruz· 1 shared Emma Betteridge· 1 shared Gavin BandiD· 1 shared Hannah Roberts· 1 shared

Activity by Year

2021-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperBioinformatics

Antony J. CutlerORCID

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1 paper

Recent·Most cited

BioinformaticsPLoS Computational BiologyPeer-reviewedAug 3, 2021

Using de novo assembly to identify structural variation of complex immune system gene regions

Jiayuan Zhang, Hannah Roberts, David Flores Santa Cruz…·Gavin Band

The paper uses long-read sequencing and de novo assembly to identify structural variation in immune system gene regions from a single individual, revealing challenges in current variant calling methods.

40 citations

humanlong-read sequencing

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