Author

Tim Harris

SV Health Investors (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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Bioinformatics· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:database / resource· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Aaron D. GitleriD· 1 shared Alessandro CulottiiD· 1 shared Alexander Baumann· 1 shared Alexander OstrovskyiD· 1 shared Alexandru MahmoudiD· 1 shared Allie Hajian· 1 shared Ana Stevens· 1 shared Andrew Rula· 1 shared

Activity by Year

2019-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetics

Aaron D. GitlerORCID

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2 papers

Recent·Most cited

Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis, Visualization, and Informatics Lab-space (AnVIL)

Michael C. Schatz, Anthony Philippakis, Enis Afgan, Eric Banks, Vincent J. Carey, Robert J. Carroll, Alessandro Culotti, Kyle Ellrott, Jeremy Goecks, Robert L. Grossman, Ira M. Hall, Kasper D. Hansen, Jonathan Lawson, Jeffrey T. Leek, Anne O’Donnell‐Luria, , Jason Walker

The paper describes AnVIL, a cloud-based platform that enables genomic data analysis without data transfer, improving security, scalability, and collaboration.

Cell Genomics · Jan 1, 2022Peer-reviewedBioinformatics

Regional collapsing of rare variation implicates specific genic regions in ALS

Sahar Gelfman, Sarah A. Dugger, Cristiane Araújo Martins Moreno, Zhong Ren, Charles J. Wolock, Neil A. Shneider, Hemali P. Phatnani, Elizabeth T. Cirulli, Brittany N. Lasseigne, Tim Harris, Tom Maniatis, Guy Armand Rouleau, Robert H. Brown, Aaron D. Gitler, R Myers, , Matthew B. Harms

The paper applies two novel collapsing methods to ALS sequencing data to identify risk regions in known ALS genes and candidate genes.

Genome Research · May 1, 2019Peer-reviewedGenetics