Author

Alex Hastie

BioNano 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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Genomics· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:whole-genome sequencing· 2 Approach:benchmark study· 1 Research Focus:benchmarking· 1 Approach:statistical model· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Alexander W Zaranek· 1 shared Ali BashiriD· 1 shared Ali Moshrefi· 1 shared Arati Sharma· 1 shared Arend SidowiD· 1 shared Barbara Miller· 1 shared Charyguly AnnageldiyeviD· 1 shared Chris Mason· 1 shared

Activity by Year

2015-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenomics

Alexander W Zaranek

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2 papers

Recent·Most cited

An Integrated Framework for Genome Analysis Reveals Numerous Previously Unrecognizable Structural Variants in Leukemia Patients' Samples

Jie Xu, Fan Song, Emily Schleicher, Christopher Pool, Darrin Bann, Max Hennessy, Kathryn Sheldon, Emma Batchelder, Charyguly Annageldiyev, Arati Sharma, Yuanyuan Chang, Alex Hastie, Barbara Miller, David Goldenberg, Shin Mineishi, , James R. Broach

The paper identifies numerous previously undetected structural variants in leukemia samples using integrated genome analysis and computational methods, revealing their impact on gene expression and patient survival.

bioRxiv · Feb 28, 2019 · PreprintGenomics

Extensive sequencing of seven human genomes to characterize benchmark reference materials

Justin M Zook, David Catoe, Jennifer McDaniel, Lindsay Vang, Noah Spies, Arend Sidow, Ziming Weng, Yuling Liu, Chris Mason, Noah Alexander, Dhruva Chandramohan, Elizabeth Henaff, Feng Chen, Erich Jaeger, Ali Moshrefi, , Sofia K

The paper presents extensive sequencing data from seven human genomes to serve as benchmark reference materials for improving sequencing technologies and variant calling.

bioRxiv · Dec 23, 2015Genomics