Author

Tera Bowers

Broad Institute

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 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 4 Research Focus:differential expression· 2 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Assay:long-read sequencing· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2

Frequent Co-Authors

Kiran V. GarimellaiD· 3 shared Maura CostelloiD· 2 shared Stacey GabrieliD· 2 shared Abebaw FekaduiD· 1 shared Alex R. HastieiD· 1 shared Alicia R. MartiniD· 1 shared Allyson Day· 1 shared Alper GokdeniD· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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3 shared papersGenomics

Kiran V. GarimellaORCID

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4 papers

Recent·Most cited

Resolution of ring chromosomes, Robertsonian translocations, and complex structural variants from long-read sequencing and telomere-to-telomere assembly

Yulia Mostovoy, Philip M. Boone, Yongqing Huang, Kiran V. Garimella, Kar‐Tong Tan, Bianca E. Russell, Monica Salani, Celine E. F. de Esch, John M. Lemanski, Benjamin Currall, Jen Hauenstein, Diane E. Lucente, Tera Bowers, Tim DeSmet, Stacey Gabriel, , Michael E. Talkowski

This paper resolves ring chromosomes, Robertsonian translocations, and complex structural variants using long-read sequencing and telomere-to-telomere assembly, revealing breakpoint structures and methylation changes.

The American Journal of Human Genetics · Nov 8, 2024Peer-reviewedGenomics

High-throughput RNA isoform sequencing using programmable cDNA concatenation

Aziz M. Al’Khafaji, Jonathan T. Smith, Kiran V. Garimella, Mehrtash Babadi, Victoria Popic, Moshe Sade-Feldman, Michael Gatzen, Siranush Sarkizova, Marc A. Schwartz, Emily M. Blaum, Allyson Day, Maura Costello, Tera Bowers, Stacey Gabriel, Eric Banks, , Nir Hacohen

This paper introduces MAS-ISO-seq, a method to boost throughput of long-read RNA sequencing for isoform discovery, showing improved detection of differentially spliced genes and cell clustering in T cells.

Nature Biotechnology · Jun 8, 2023Peer-reviewedGenetics

Transcriptome variation in human tissues revealed by long-read sequencing

Dafni A. Glinos, Garrett Garborcauskas, Paul Hoffman, Nava Ehsan, Lihua Jiang, Alper Gokden, Xiaoguang Dai, François Aguet, Kathleen L. Brown, Kiran V. Garimella, Tera Bowers, Maura Costello, Kristin Ardlie, Ruiqi Jian, Nathan R. Tucker, , Beryl B. Cummings

The paper uses long-read RNA-seq data to identify new transcripts and develop a tool to analyze genetic effects on transcript structure, revealing insights into splicing regulation and variant interpretation.

Nature · Aug 3, 2022Peer-reviewedGenomics

Low-coverage sequencing cost-effectively detects known and novel variation in underrepresented populations

Alicia R. Martin, Elizabeth G. Atkinson, Sinéad B. Chapman, Anne Stevenson, Rocky E. Stroud, Tamrat Abebe, Dickens Howard Akena, Melkam Alemayehu Kebede, Fred K. Ashaba, Lukoye Atwoli, Tera Bowers, Lori Beth Chibnik, Mark J. Daly, Timothy DeSmet, Sheila Dodge, , Zukiswa Zingela

This study shows low-coverage sequencing is more accurate and cost-effective than GWAS arrays for detecting genetic variation in diverse African populations.

The American Journal of Human Genetics · Mar 25, 2021Peer-reviewedGenomics