Peter A Audano (P A Audano)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 36

Top Topics

Single Molecule

High Throughput Sequencing

Genome Wide Association Study

Top Venues

Genome research

Nature communications

bioRxiv : the preprint server for biology

Science (New York, N.Y.)

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

Publications

Peter A Audano, Christine R Beck
Small polymorphisms are a source of ancestral bias in structural variant breakpoint placement. Genome research 34 (1) (2024)
Peter A Audano, Christine R Beck
Small polymorphisms are a source of ancestral bias in structural variant breakpoint placement. Genome research (2024)
Medhat Mahmoud, Y Huang, K Garimella, Peter A Audano, W Wan, N Prasad, Robert E Handsaker, S Hall, A Pionzio, Michael C Schatz, Michael E Talkowski, Evan E Eichler, Shawn E Levy, Fritz J Sedlazeck
Utility of long-read sequencing for All of Us. Nature communications 15 (1) (2024)
Peter A Audano, Christine R Beck
Small polymorphisms are a source of ancestral bias in structural variant breakpoint placement. Genome research 34 (1) (2024)
Peter A Audano, Christine R Beck
Small polymorphisms are a source of ancestral bias in structural variant breakpoint placement. Genome research 34 (1) (2024)
Medhat Mahmoud, Y Huang, K Garimella, Peter A Audano, W Wan, N Prasad, Robert E Handsaker, S Hall, A Pionzio, Michael C Schatz, Michael E Talkowski, Evan E Eichler, Shawn E Levy, Fritz J Sedlazeck
Utility of long-read sequencing for All of Us. Nature communications 15 (1) (2024)
Peter A Audano, Christine R Beck
Small polymorphisms are a source of ancestral bias in structural variant breakpoint placement. Genome research (2024)
Medhat Mahmoud, Y Huang, K Garimella, Peter A Audano, W Wan, N Prasad, Robert E Handsaker, S Hall, A Pionzio, Michael C Schatz, Michael E Talkowski, Evan E Eichler, Shawn E Levy, Fritz J Sedlazeck
Utility of long-read sequencing for All of Us. Nature communications 15 (1) (2024)
Peter A Audano, Christine R Beck
Small polymorphisms are a source of ancestral bias in structural variant breakpoint placement. Genome research 34 (1) (2024)
Peter A Audano, Christine R Beck
Small polymorphisms are a source of ancestral bias in structural variant breakpoint placement. Genome research 34 (1) (2024)
Peter A Audano, Christine R Beck
Small polymorphisms are a source of ancestral bias in structural variant breakpoint placement. Genome research 34 (1) (2024)
Peter A Audano, Christine R Beck
Small polymorphisms are a source of ancestral bias in structural variant breakpoint placement. Genome research (2024)
Medhat Mahmoud, Y Huang, K Garimella, Peter A Audano, W Wan, N Prasad, Robert E Handsaker, S Hall, A Pionzio, Michael C Schatz, Michael E Talkowski, Evan E Eichler, Shawn E Levy, Fritz J Sedlazeck
Utility of long-read sequencing for All of Us. Nature communications 15 (1) (2024)
Peter A Audano, Christine R Beck
Small polymorphisms are a source of ancestral bias in structural variant breakpoint placement. Genome research 34 (1) (2024)
Medhat Mahmoud, Y Huang, K Garimella, Peter A Audano, W Wan, N Prasad, Robert E Handsaker, S Hall, A Pionzio, Michael C Schatz, Michael E Talkowski, Evan E Eichler, Shawn E Levy, Fritz J Sedlazeck
Utility of long-read sequencing for All of Us. Nature communications 15 (1) (2024)
William T Harvey, Peter Ebert, Jana Ebler, Peter A Audano, Katherine M Munson, Kendra Hoekzema, David Porubsky, Christine R Beck, Tobias Marschall, Kiran V Garimella, Evan E Eichler
Whole-genome long-read sequencing downsampling and its effect on variant-calling precision and recall. Genome research 33 (12) (2023)
William T Harvey, Peter Ebert, Jana Ebler, Peter A Audano, Katherine M Munson, Kendra Hoekzema, David Porubsky, Christine R Beck, Tobias Marschall, Kiran V Garimella, Evan E Eichler
Whole-genome long-read sequencing downsampling and its effect on variant calling precision and recall. bioRxiv : the preprint server for biology (2023)
Peter A Audano, Christine R Beck
Small allelic variants are a source of ancestral bias in structural variant breakpoint placement. bioRxiv : the preprint server for biology (2023)
William T Harvey, Peter Ebert, Jana Ebler, Peter A Audano, Katherine M Munson, Kendra Hoekzema, David Porubsky, Christine R Beck, Tobias Marschall, Kiran V Garimella, Evan E Eichler
Whole-genome long-read sequencing downsampling and its effect on variant-calling precision and recall. Genome research 33 (12) (2023)
William T Harvey, Peter Ebert, Jana Ebler, Peter A Audano, Katherine M Munson, Kendra Hoekzema, David Porubsky, Christine R Beck, Tobias Marschall, Kiran V Garimella, Evan E Eichler
Whole-genome long-read sequencing downsampling and its effect on variant-calling precision and recall. Genome research 33 (12) (2023)
William T Harvey, Peter Ebert, Jana Ebler, Peter A Audano, Katherine M Munson, Kendra Hoekzema, David Porubsky, Christine R Beck, Tobias Marschall, Kiran V Garimella, Evan E Eichler
Whole-genome long-read sequencing downsampling and its effect on variant-calling precision and recall. Genome research 33 (12) (2023)
William T Harvey, Peter Ebert, Jana Ebler, Peter A Audano, Katherine M Munson, Kendra Hoekzema, David Porubsky, Christine R Beck, Tobias Marschall, Kiran V Garimella, Evan E Eichler
Whole-genome long-read sequencing downsampling and its effect on variant-calling precision and recall. Genome research 33 (12) (2023)
William T Harvey, Peter Ebert, Jana Ebler, Peter A Audano, Katherine M Munson, Kendra Hoekzema, David Porubsky, Christine R Beck, Tobias Marschall, Kiran V Garimella, Evan E Eichler
Whole-genome long-read sequencing downsampling and its effect on variant-calling precision and recall. Genome research 33 (12) (2023)
William T Harvey, Peter Ebert, Jana Ebler, Peter A Audano, Katherine M Munson, Kendra Hoekzema, David Porubsky, Christine R Beck, Tobias Marschall, Kiran V Garimella, Evan E Eichler
Whole-genome long-read sequencing downsampling and its effect on variant-calling precision and recall. Genome research 33 (12) (2023)
William T Harvey, Peter Ebert, Jana Ebler, Peter A Audano, Katherine M Munson, Kendra Hoekzema, David Porubsky, Christine R Beck, Tobias Marschall, Kiran V Garimella, Evan E Eichler
Whole-genome long-read sequencing downsampling and its effect on variant-calling precision and recall. Genome research 33 (12) (2023)
William T Harvey, Peter Ebert, Jana Ebler, Peter A Audano, Katherine M Munson, Kendra Hoekzema, David Porubsky, Christine R Beck, Tobias Marschall, Kiran V Garimella, Evan E Eichler
Whole-genome long-read sequencing downsampling and its effect on variant calling precision and recall. bioRxiv : the preprint server for biology (2023)
William T Harvey, Peter Ebert, Jana Ebler, Peter A Audano, Katherine M Munson, Kendra Hoekzema, David Porubsky, Christine R Beck, Tobias Marschall, Kiran V Garimella, Evan E Eichler
Whole-genome long-read sequencing downsampling and its effect on variant calling precision and recall. bioRxiv : the preprint server for biology (2023)
Pille Hallast, Peter Ebert, Mark Loftus, Feyza Yilmaz, Peter A Audano, Glennis A Logsdon, Marc Jan Bonder, Weichen Zhou, Wolfram Höps, Kwondo Kim, Chong Li, Savannah J Hoyt, Philip C Dishuck, David Porubsky, Fotios Tsetsos, Jee Young Kwon, Qihui Zhu, Katherine M Munson, Patrick Hasenfeld, William T Harvey, Alexandra P Lewis, Jennifer Kordosky, Kendra Hoekzema, null null, Rachel J O'Neill, Jan O Korbel, Chris Tyler-Smith, Evan E Eichler, Xinghua Shi, Christine R Beck, Tobias Marschall, Miriam K Konkel, Charles Lee
Assembly of 43 human Y chromosomes reveals extensive complexity and variation. Nature (2023)
William T Harvey, Peter Ebert, Jana Ebler, Peter A Audano, Katherine M Munson, Kendra Hoekzema, David Porubsky, Christine R Beck, Tobias Marschall, Kiran V Garimella, Evan E Eichler
Whole-genome long-read sequencing downsampling and its effect on variant-calling precision and recall. Genome research 33 (12) (2023)
William T Harvey, Peter Ebert, Jana Ebler, Peter A Audano, Katherine M Munson, Kendra Hoekzema, David Porubsky, Christine R Beck, Tobias Marschall, Kiran V Garimella, Evan E Eichler
Whole-genome long-read sequencing downsampling and its effect on variant-calling precision and recall. Genome research 33 (12) (2023)
Jiadong Lin, Songbo Wang, Peter A Audano, Deyu Meng, Jacob I Flores, Walter A Kosters, Xiaofei Yang, Peng Jia, Tobias Marschall, Christine R Beck, Kai Ye
SVision: a deep learning approach to resolve complex structural variants. Nature methods 19 (10) (2022)
Parithi Balachandran, Isha A Walawalkar, Jacob I Flores, Jacob N Dayton, Peter A Audano, Christine R Beck
Transposable element-mediated rearrangements are prevalent in human genomes. Nature communications 13 (1) (2022)
Peter Ebert, Peter A Audano, Qihui Zhu, Bernardo Rodriguez-Martin, David Porubsky, Marc Jan Bonder, Arvis Sulovari, Jana Ebler, Weichen Zhou, Rebecca Serra Mari, Feyza Yilmaz, Xuefang Zhao, PingHsun Hsieh, Joyce Lee, Sushant Kumar, Jiadong Lin, Tobias Rausch, Yu Chen, Jingwen Ren, Martin Santamarina, Wolfram Höps, Hufsah Ashraf, Nelson T Chuang, Xiaofei Yang, Katherine M Munson, Alexandra P Lewis, Susan Fairley, Luke J Tallon, Wayne E Clarke, Anna O Basile, Marta Byrska-Bishop, André Corvelo, Uday S Evani, Tsung-Yu Lu, Mark J P Chaisson, Junjie Chen, Chong Li, Harrison Brand, Aaron M Wenger, Maryam Ghareghani, William T Harvey, Benjamin Raeder, Patrick Hasenfeld, Allison A Regier, Haley J Abel, Ira M Hall, Paul Flicek, Oliver Stegle, Mark B Gerstein, Jose M C Tubio, Zepeng Mu, Yang I Li, Xinghua Shi, Alex R Hastie, Kai Ye, Zechen Chong, Ashley D Sanders, Michael C Zody, Michael E Talkowski, Ryan E Mills, Scott E Devine, Charles Lee, Jan O Korbel, Tobias Marschall, Evan E Eichler
Haplotype-resolved diverse human genomes and integrated analysis of structural variation. Science (New York, N.Y.) 372 (6537) (2021)
Wesley C Warren, Ronald Alan Harris, Marina Haukness, Ian T Fiddes, Shwetha C Murali, Jason D Fernandes, Philip C Dishuck, Jessica M Storer, Muthuswamy Raveendran, LaDeana W Hillier, David Porubsky, Yafei Mao, David Gordon, Mitchell R Vollger, Alexandra P Lewis, Katherine M Munson, Elizabeth DeVogelaere, Joel Armstrong, Mark E Diekhans, Jerilyn A Walker, Chad Tomlinson, Tina A Graves-Lindsay, Milinn Kremitzki, Sofie R Salama, Peter A Audano, Merly Escalona, Nicholas W Maurer, Francesca Antonacci, Ludovica Mercuri, Flavia Angela Maria Maggiolini, Claudia Rita Catacchio, Jason G Underwood, David H O'Connor, Ashley D Sanders, Jan O Korbel, Betsy M Ferguson, H Michael Kubisch, Louis J Picker, Ned H Kalin, Douglas Rosene, Jon E Levine, David H Abbott, Stanton B Gray, Mar M Sanchez, Zsofia A Kovacs-Balint, Joseph W Kemnitz, Sara M Thomasy, Jeffrey A Roberts, Erin L Kinnally, John P Capitanio, Jesse A G Skene, Michael Louis Platt, Shelley A Cole, Richard E Green, Mario Ventura, Roger W Wiseman, Benedict Paten, Mark A Batzer, Jeffrey Rogers, Evan E Eichler
Sequence diversity analyses of an improved rhesus macaque genome enhance its biomedical utility. Science (New York, N.Y.) 370 (6523) (2021)
Mark J P Chaisson, Ashley D Sanders, Xuefang Zhao, Ankit Malhotra, David Porubsky, Tobias Rausch, Eugene J Gardner, Oscar L Rodriguez, Li Guo, Ryan L Collins, Xian Fan, Jia Wen, Robert E Handsaker, Susan Fairley, Zev N Kronenberg, Xiangmeng Kong, Fereydoun Hormozdiari, Dillon Lee, Aaron M Wenger, Alex R Hastie, Danny Antaki, Thomas Anantharaman, Peter A Audano, Harrison Brand, Stuart Cantsilieris, Han Cao, Eliza Cerveira, Chong Chen, Xintong Chen, Chen-Shan Chin, Zechen Chong, Nelson T Chuang, Christine C Lambert, Deanna M Church, Laura Clarke, Andrew Farrell, Joey Flores, Timur Galeev, David U Gorkin, Madhusudan Gujral, Victor Guryev, William Haynes Heaton, Jonas Korlach, Sushant Kumar, Jee Young Kwon, Ernest T Lam, Jong Eun Lee, Joyce Lee, Wan-Ping Lee, Sau Peng Lee, Shantao Li, Patrick Marks, Karine Viaud-Martinez, Sascha Meiers, Katherine M Munson, Fábio C P Navarro, Bradley J Nelson, Conor Nodzak, Amina Noor, Sofia Kyriazopoulou-Panagiotopoulou, Andy W C Pang, Yunjiang Qiu, Gabriel Rosanio, Mallory Ryan, Adrian Stütz, Diana C J Spierings, Alistair Ward, AnneMarie E Welch, Ming Xiao, Wei Xu, Chengsheng Zhang, Qihui Zhu, Xiangqun Zheng-Bradley, Ernesto Lowy-Gallego, Sergei Yakneen, Steven McCarroll, Goo Jun, Li Ding, Chong Lek Koh, Bing Ren, Paul Flicek, Ken Chen, Mark B Gerstein, Pui-Yan Kwok, Peter M Lansdorp, Gabor T Marth, Jonathan Sebat, Xing-Hua Shi, Ali Bashir, Kai Ye, Scott E Devine, Michael E Talkowski, Ryan E Mills, Tobias Marschall, Jan O Korbel, Evan E Eichler, Charles Lee
Multi-platform discovery of haplotype-resolved structural variation in human genomes. Nature communications 10 (1) (2019)
Mitchell R Vollger, Glennis A Logsdon, Peter A Audano, Arvis Sulovari, David Porubsky, Paul Peluso, Aaron M Wenger, Gregory T Concepcion, Zev N Kronenberg, Katherine M Munson, Carl Baker, Ashley D Sanders, Diana C J Spierings, Peter M Lansdorp, Urvashi Surti, Michael W Hunkapiller, Evan E Eichler
Improved assembly and variant detection of a haploid human genome using single-molecule, high-fidelity long reads. Annals of human genetics 84 (2) (2019)