Author

Adrian N. Fehr

10X Genomics (United States)

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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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Assay:DNA methylation· 1 Research Focus:genome assembly· 1 Organism:human· 1

Frequent Co-Authors

Adam J. LoweiD· 1 shared Álvaro Martínez BarrioiD· 1 shared Andrew D.F. PriceiD· 1 shared Andrew Wei Xu· 1 shared Ariel Royall· 1 shared Benjamin Haibe‐KainsiD· 1 shared Bill K. Lin· 1 shared Brendan D. Galvin· 1 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenomics

Adam J. LoweORCID

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Author profile →

2 papers

Recent·Most cited

Evaluation of ensilication technology for ambient DNA preservation

Michael Blas, Celeste Yu, Farnoosh Abbas Aghababazadeh, Vanessa Hoelscher, Marcus Volz, Linden L. Morales, Kaytee Jarolik, Xiuhua Dong, Sheila M. Dobin, Tuula Rantasalo, Tatu Hirvonen, Juha-Pekka Pursiheimo, Nea Laine, Nils Homer, Cassandra Chamoun, , Philippe Lucien Bedard

This paper evaluates ensilication technology for ambient DNA preservation, finding it maintains sequencing fidelity and reduces artifacts compared to frozen storage.

NAR Molecular Medicine · Jan 1, 2026Peer-reviewedGenetic & Genomic Medicine

Resolving the Full Spectrum of Human Genome Variation using Linked-Reads

Patrick Marks, Sarah Garcia, Álvaro Martínez Barrio, Kamila Belhocine, Jorge Bernate, Rajiv Bharadwaj, Keith P. Bjornson, Claudia Catalanotti, Josh Delaney, Adrian N. Fehr, Ian T. Fiddes, Brendan D. Galvin, Haynes Heaton, Jill Herschleb, Christopher M. Hindson, , Deanna M. Church

This paper introduces Linked-Reads as a method to comprehensively analyze genome variation, showing it can detect both small and large variants and reconstruct haplotypes more effectively than short-read sequencing.

Genome Research · Apr 1, 2019Peer-reviewedGenomics