Tanner D Jensen

Publication Activity (10 Years)

Years Active: 2024-2024
Publications (10 Years): 11

Top Topics

Bioinformatics Analysis

Congenital Heart Disease

Top Venues

medRxiv : the preprint server for health sciences

This page only lists publications with an associated author ORCID identifier.

Publications

Tanner D Jensen, Bohan Ni, Chloe Reuter, John E Gorzynski, Sarah Fazal, Devon E Bonner, Rachel Allison Ungar, Pagé C Goddard, Archana Natarajan Raja, Euan A Ashley, Jonathan A Bernstein, Stephan Zuchner, null null, Michael D Greicius, Stephen B Montgomery, Michael C Schatz, Matthew T Wheeler, Alexis J Battle
Integration of transcriptomics and long-read genomics prioritizes structural variants in rare disease. medRxiv : the preprint server for health sciences (2024)
Rachel Allison Ungar, Pagé C Goddard, Tanner D Jensen, Fabien Degalez, Kevin S Smith, Christopher A Jin, null null, Devon E Bonner, Jonathan A Bernstein, Matthew T Wheeler, Stephen B Montgomery
Impact of genome build on RNA-seq interpretation and diagnostics. medRxiv : the preprint server for health sciences (2024)
Jonas A Gustafson, Sophia B Gibson, Nikhita Damaraju, Miranda Perez-Galey Zalusky, Kendra Hoekzema, David Twesigomwe, Lei Yang, Anthony A Snead, Phillip Andrew Richmond, Wouter De Coster, Nathan D Olson, Andrea Guarracino, Qiuhui Li, Angela L Miller, Joy Goffena, Zachery Anderson, Sophie Hr Storz, Sydney A Ward, Maisha Sinha, Claudia Gonzaga-Jauregui, Wayne E Clarke, Anna O Basile, André Corvelo, Catherine E Reeves, Adrienne Helland, Rajeeva Lochan Musunuri, Mahler Revsine, Karynne E Patterson, Cate Paschal, Christina Zakarian, Sara Goodwin, Tanner D Jensen, Esther Robb, null null, null null, null null, W Richard McCombie, Fritz J Sedlazeck, Justin M Zook, Stephen B Montgomery, Erik P Garrison, Mikhail Kolmogorov, Michael C Schatz, Richard N McLaughlin, Harriet Dashnow, Michael C Zody, Matthew William Loose, Miten Jain, Evan E Eichler, Danny E Miller
Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variation. medRxiv : the preprint server for health sciences (2024)
Tanner D Jensen, Bohan Ni, Chloe M Reuter, John E Gorzynski, Sarah Fazal, Devon E Bonner, Rachel Allison Ungar, Pagé C Goddard, Archana Natarajan Raja, Euan A Ashley, Jonathan A Bernstein, Stephan Zuchner, null null, Michael D Greicius, Stephen B Montgomery, Michael C Schatz, Matthew T Wheeler, Alexis J Battle
Integration of transcriptomics and long-read genomics prioritizes structural variants in rare disease. medRxiv : the preprint server for health sciences (2024)
Rachel Allison Ungar, Pagé C Goddard, Tanner D Jensen, Fabien Degalez, Kevin S Smith, Christopher A Jin, null null, Devon E Bonner, Jonathan A Bernstein, Matthew T Wheeler, Stephen B Montgomery
Impact of genome build on RNA-seq interpretation and diagnostics. medRxiv : the preprint server for health sciences (2024)
Rachel Allison Ungar, Pagé C Goddard, Tanner D Jensen, Fabien Degalez, Kevin S Smith, Christopher A Jin, null null, Devon E Bonner, Jonathan A Bernstein, Matthew T Wheeler, Stephen B Montgomery
Impact of genome build on RNA-seq interpretation and diagnostics. medRxiv : the preprint server for health sciences (2024)
Jonas A Gustafson, Sophia B Gibson, Nikhita Damaraju, Miranda Perez-Galey Zalusky, Kendra Hoekzema, David Twesigomwe, Lei Yang, Anthony A Snead, Phillip Andrew Richmond, Wouter De Coster, Nathan D Olson, Andrea Guarracino, Qiuhui Li, Angela L Miller, Joy Goffena, Zachery Anderson, Sophie Hr Storz, Sydney A Ward, Maisha Sinha, Claudia Gonzaga-Jauregui, Wayne E Clarke, Anna O Basile, André Corvelo, Catherine E Reeves, Adrienne Helland, Rajeeva Lochan Musunuri, Mahler Revsine, Karynne E Patterson, Cate R Paschal, Christina Zakarian, Sara Goodwin, Tanner D Jensen, Esther Robb, null null, null null, null null, W Richard McCombie, Fritz J Sedlazeck, Justin M Zook, Stephen B Montgomery, Erik P Garrison, Mikhail Kolmogorov, Michael C Schatz, Richard N McLaughlin, Harriet Dashnow, Michael C Zody, Matthew William Loose, Miten Jain, Evan E Eichler, Danny E Miller
Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variation. medRxiv : the preprint server for health sciences (2024)
Rachel Allison Ungar, Pagé C Goddard, Tanner D Jensen, Fabien Degalez, Kevin S Smith, Christopher A Jin, null null, Devon E Bonner, Jonathan A Bernstein, Matthew T Wheeler, Stephen B Montgomery
Impact of genome build on RNA-seq interpretation and diagnostics. medRxiv : the preprint server for health sciences (2024)
Rachel Allison Ungar, Pagé C Goddard, Tanner D Jensen, Fabien Degalez, Kevin S Smith, Christopher A Jin, null null, Devon E Bonner, Jonathan A Bernstein, Matthew T Wheeler, Stephen B Montgomery
Impact of genome build on RNA-seq interpretation and diagnostics. medRxiv : the preprint server for health sciences (2024)
Rachel Allison Ungar, Pagé C Goddard, Tanner D Jensen, Fabien Degalez, Kevin S Smith, Christopher A Jin, null null, Devon E Bonner, Jonathan A Bernstein, Matthew T Wheeler, Stephen B Montgomery
Impact of genome build on RNA-seq interpretation and diagnostics. medRxiv : the preprint server for health sciences (2024)
Tanner D Jensen, Bohan Ni, Chloe M Reuter, John E Gorzynski, Sarah Fazal, Devon E Bonner, Rachel Allison Ungar, Pagé C Goddard, Archana Natarajan Raja, Euan A Ashley, Jonathan A Bernstein, Stephan Zuchner, null null, Michael D Greicius, Stephen B Montgomery, Michael C Schatz, Matthew T Wheeler, Alexis J Battle
Integration of transcriptomics and long-read genomics prioritizes structural variants in rare disease. medRxiv : the preprint server for health sciences (2024)