Author

Andrew Wei Xu

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

Click to filter author papers

Genomics· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Research Focus:genome assembly· 1 Organism:human· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

David A. StaffordiD· 2 shared Deanna M. ChurchiD· 2 shared Jill Herschleb· 2 shared Patrick MarksiD· 2 shared Sarah Garcia· 2 shared Stephen R. WilliamsiD· 2 shared Adam J. LoweiD· 1 shared Adrian N. Fehr· 1 shared

Activity by Year

2017-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenomics

David A. StaffordORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

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

Linked-Read sequencing resolves complex structural variants

Sarah Garcia, Stephen R. Williams, Andrew Wei Xu, Jill Herschleb, Patrick Marks, David A. Stafford, Deanna M. Church

This study evaluates Linked-Read sequencing for detecting structural variants, finding it can identify most known events with low sequencing depth and provides breakpoint resolution.

bioRxiv · Dec 8, 2017 · PreprintGenomics