Author

Faaiz Quaisar

University of Washington

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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Genomics· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Organism:human· 1 Organism:mouse· 1 Assay:scRNA-seq· 1 Research Focus:software / tool· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Jay ShendureiD· 2 shared Jonas KoeppeliD· 2 shared Riza M. DazaiD· 2 shared Sudarshan PinglayiD· 2 shared Aidan KeithiD· 1 shared David S. LeeiD· 1 shared Eleftheria AnastasiaiD· 1 shared Jean‐Benoît LalanneiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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2 shared papersGenomics

Jay ShendureORCID

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2 papers

Recent·Most cited

Gigabase-scale deletion scanning of the human genome

Jonas Koeppel, Aidan Keith, Samantha R. Sgrizzi, PeiXi Chen, Riza M. Daza, Faaiz Quaisar, Eleftheria Anastasia, Zihao Song, Jay Shendure, Sudarshan Pinglay

This paper introduces Shred-seq, a method to scan large-scale deletions in the human genome, revealing essential regions including noncoding sequences and establishing a lower bound for viability.

bioRxiv · Jun 2, 2026 · PreprintGenomics

Multiplex generation and single cell analysis of structural variants in a mammalian genome

Sudarshan Pinglay, Jean‐Benoît Lalanne, Riza M. Daza, Sanjay V. Kottapalli, Faaiz Quaisar, Jonas Koeppel, Riddhiman K. Garge, Xiaoyi Li, David S. Lee, Jay Shendure

This paper introduces Genome-Shuffle-seq, a method for generating and mapping structural variants in mammalian genomes, and demonstrates its application in mouse embryonic stem cells.

Science · Jan 30, 2025Peer-reviewedGenomics