Author

Tanner Hagelstrom

Illumina (United States)

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Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Aditi Chawla· 1 shared Ana Lisa Taylor TavaresiD· 1 shared Andrew David MumfordiD· 1 shared Anette E. SchragiD· 1 shared Angela Douglas· 1 shared Anna C. NeediD· 1 shared Antonio Rueda Martin· 1 shared Arianna TucciiD· 1 shared

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2020-2020 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Aditi Chawla

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1 paper

Recent·Most cited

GenomicsbioRxivPreprintNov 6, 2020

Whole genome sequencing for diagnosis of neurological repeat expansion disorders

Kristina Ibáñez, James M. Polke, Tanner Hagelstrom…·Arianna Tucci

This study demonstrates that whole genome sequencing can effectively detect repeat expansions in neurological disorders with high sensitivity and specificity, enabling diagnosis in previously undiagnosed patients.

6 citations

humanwhole-genome sequencing

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