Author

Rob Furatero

New York Genome Center

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· 3

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:human· 3 Research Focus:variant calling· 3 Assay:whole-genome sequencing· 3 Organism:mouse· 1

Frequent Co-Authors

Dan Avi LandauiD· 3 shared Søren GermeriD· 3 shared Adam J. WidmaniD· 2 shared Alexandre Pellan ChengiD· 2 shared Alexi M. RunnelsiD· 2 shared Ariel Jaimovich· 2 shared Ashish SaxenaiD· 2 shared Dennis J. YuaniD· 2 shared

Activity by Year

2022-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenomics

Dan Avi LandauORCID

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3 papers

Recent·Most cited

A comprehensive view of somatic mosaicism by single-cell DNA analysis

Lovelace J. Luquette, Tim H. H. Coorens, Abhiram Natu, Milovan Šuvakov, Ann H. Caplin, Mee Sook Jun, Alisa Mo, Joe Pelt, Lisa Anderson, Michele Berselli, Sravya Venkata Bhamidipati, Thomas P. Blanchard, Joseph Brew, Hye-Jung E. Chun, Hyunbin Chun, , Alexej S. Abyzov

The paper uses single-cell DNA sequencing to analyze somatic mosaicism in postmortem lung and colon tissues, revealing mutation heterogeneity, chromosomal abnormalities, and cellular ancestry.

bioRxiv · Oct 31, 2025 · PreprintGenomics

Paired plus-minus sequencing is an ultra-high throughput and accurate method for dual strand sequencing of DNA molecules

Alexandre Pellan Cheng, Itai Rusinek, Aaron Sossin, Adam J. Widman, Eti Meiri, Gat Krieger, Ori Hirschberg, Doron Shem Tov, Shlomit Gilad, Ariel Jaimovich, Omer Barad, Sammantha Avaylon, Srinivas Rajagopalan, Abigail G. Thress, Catherine J. Potenski, , Dan Avi Landau

This paper introduces ppmSeq, a sequencing technology that improves accuracy and efficiency in detecting SNVs by sequencing both DNA strands, showing superior performance in clinical applications like ctDNA detection.

bioRxiv · Aug 11, 2025 · PreprintGenomics

Whole genome error-corrected sequencing for sensitive circulating tumor DNA cancer monitoring

Alexandre Pellan Cheng, Adam J. Widman, Anushri Arora, Itai Rusinek, William F. Hooper, Rebecca L. Murray, Daniel Halmos, Theophile Langanay, Giorgio Inghirami, Søren Germer, Melissa Marton, Dina Manaa, Adrienne Helland, Rob Furatero, Jaime McClintock, , Dan Avi Landau

This study applies low-cost whole genome sequencing to detect circulating tumor DNA at high sensitivity in plasma samples, achieving error rates as low as 10^-7 and enabling cancer monitoring without matched tumor sequencing.

bioRxiv · Nov 17, 2022 · PreprintGenomics