Author

Michael Saghbini

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:experimental assay· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Han CaoiD· 2 shared Alex Hastie· 1 shared Alex R. HastieiD· 1 shared Alexander W Zaranek· 1 shared Ali BashiriD· 1 shared Ali Moshrefi· 1 shared Andy Wing Chun PangiD· 1 shared Arend SidowiD· 1 shared

Activity by Year

2015-2017 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersGenomics

Han CaoORCID

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2 papers

Recent·Most cited

Rapid Automated Large Structural Variation Detection in a Diploid Genome by NanoChannel Based Next-Generation Mapping

Alex R. Hastie, Ernest T. Lam, Andy Wing Chun Pang, Xinyue Zhang, Warren Andrews, Joyce Lee, Tiffany Y Liang, Jian Wang, Xiang Zhou, Zhanyang Zhu, Thomas Anantharaman, Željko Džakula, Sven Bocklandt, Urvashi Surti, Michael Saghbini, , Han Cao

The paper introduces a method to detect large structural variants in diploid genomes using Bionano Genomics next-generation mapping, achieving high resolution and throughput.

bioRxiv · Feb 14, 2017 · 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