Christine R Beck

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 32

Top Topics

Single Molecule

Genome Wide Association Study

Mitochondrial Dna

Top Venues

Genome research

bioRxiv : the preprint server for biology

Science advances

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)
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)
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)
DongAhn Yoo, Arang Rhie, Prajna Hebbar, Francesca Antonacci, Glennis A Logsdon, Steven Jared Solar, Dmitry Antipov, Brandon D Pickett, Yana Safonova, Francesco Montinaro, Yanting Luo, Joanna Malukiewicz, Jessica M Storer, Jiadong Lin, Abigail N Sequeira, Riley J Mangan, Glenn Hickey, Graciela Monfort Anez, Parithi Balachandran, Anton Bankevich, Christine R Beck, Arjun Biddanda, Matthew Borchers, Gerard G Bouffard, Emry Brannan, Shelise Y Brooks, Lucia Carbone, Laura Carrel, Yongwook Choi, Juyun Crawford, Mark Diekhans, Eric Engelbrecht, Cedric Feschotte, Giulio Formenti, Gage H Garcia, Luciana de Gennaro, David M Gilbert, Richard E Green, Andrea Guarracino, Ishaan Gupta, Diana Haddad, Junmin Han, Robert S Harris, Gabrielle A Hartley, William T Harvey, Michael Hiller, Kendra Hoekzema, Marlys L Houck, Hyeonsoo Jeong, Kaivan Kamali, Manolis Kellis, Bryce Kille, Chul Lee, Youngho Lee, William D Lees, Alexandra P Lewis, Qiuhui Li, Mark Loftus, Yong Hwee Eddie Loh, Hailey Loucks, Jian Ma, Yafei Mao, Juan F I Martinez, Patrick Masterson, Rajiv C McCoy, Barbara McGrath, Sean McKinney, Britta S Meyer, Karen H Miga, Saswat Kumar Mohanty, Katherine M Munson, Karol Pal, Matthew W Pennell, Pavel A Pevzner, David Porubsky, Tamara Potapova, Francisca R Ringeling, Joana L Rocha, Oliver A Ryder, Samuel Sacco, Swati Saha, Takayo Sasaki, Michael C Schatz, Nicholas J Schork, Cole Shanks, Linnéa Smeds, Dongmin R Son, Cynthia Steiner, Alexander P Sweeten, Michael G Tassia, Françoise Thibaud-Nissen, Edmundo Torres-González, Mihir Trivedi, Wenjie Wei, Julie Wertz, Muyu Yang, Panpan Zhang, Shilong Zhang, Yang Zhang, Zhenmiao Zhang, Sarah A Zhao, Yixin Zhu, Erich D Jarvis, Jennifer L Gerton, Iker Rivas-González, Benedict Paten, Zachary Alfano Szpiech, Christian D Huber, Tobias L Lenz, Miriam K Konkel, Soojin V Yi, Stefan Canzar, Corey T Watson, Peter H Sudmant, Erin K Molloy, Erik Garrison, Craig B Lowe, Mario Ventura, Rachel J O'Neill, Sergey Koren, Kateryna D Makova, Adam M Phillippy, Evan E Eichler
Complete sequencing of ape genomes. bioRxiv : the preprint server for biology (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)
DongAhn Yoo, Arang Rhie, Prajna Hebbar, Francesca Antonacci, Glennis A Logsdon, Steven Jared Solar, Dmitry Antipov, Brandon D Pickett, Yana Safonova, Francesco Montinaro, Yanting Luo, Joanna Malukiewicz, Jessica M Storer, Jiadong Lin, Abigail N Sequeira, Riley J Mangan, Glenn Hickey, Graciela Monfort Anez, Parithi Balachandran, Anton Bankevich, Christine R Beck, Arjun Biddanda, Matthew Borchers, Gerard G Bouffard, Emry Brannan, Shelise Y Brooks, Lucia Carbone, Laura Carrel, Yongwook Choi, Juyun Crawford, Mark Diekhans, Eric Engelbrecht, Cedric Feschotte, Giulio Formenti, Gage H Garcia, Luciana de Gennaro, David M Gilbert, Richard E Green, Andrea Guarracino, Ishaan Gupta, Diana Haddad, Junmin Han, Robert S Harris, Gabrielle A Hartley, William T Harvey, Michael Hiller, Kendra Hoekzema, Marlys L Houck, Hyeonsoo Jeong, Kaivan Kamali, Manolis Kellis, Bryce Kille, Chul Lee, Youngho Lee, William D Lees, Alexandra P Lewis, Qiuhui Li, Mark Loftus, Yong Hwee Eddie Loh, Hailey Loucks, Jian Ma, Yafei Mao, Juan F I Martinez, Patrick Masterson, Rajiv C McCoy, Barbara McGrath, Sean McKinney, Britta S Meyer, Karen H Miga, Saswat Kumar Mohanty, Katherine M Munson, Karol Pal, Matthew W Pennell, Pavel A Pevzner, David Porubsky, Tamara Potapova, Francisca R Ringeling, Joana L Rocha, Oliver A Ryder, Samuel Sacco, Swati Saha, Takayo Sasaki, Michael C Schatz, Nicholas J Schork, Cole Shanks, Linnéa Smeds, Dongmin R Son, Cynthia Steiner, Alexander P Sweeten, Michael G Tassia, Françoise Thibaud-Nissen, Edmundo Torres-González, Mihir Trivedi, Wenjie Wei, Julie Wertz, Muyu Yang, Panpan Zhang, Shilong Zhang, Yang Zhang, Zhenmiao Zhang, Sarah A Zhao, Yixin Zhu, Erich D Jarvis, Jennifer L Gerton, Iker Rivas-González, Benedict Paten, Zachary Alfano Szpiech, Christian D Huber, Tobias L Lenz, Miriam K Konkel, Soojin V Yi, Stefan Canzar, Corey T Watson, Peter H Sudmant, Erin K Molloy, Erik Garrison, Craig B Lowe, Mario Ventura, Rachel J O'Neill, Sergey Koren, Kateryna D Makova, Adam M Phillippy, Evan E Eichler
Complete sequencing of ape genomes. bioRxiv : the preprint server for biology (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)
Diogo F T Veiga, Alex Nesta, Yuqi Zhao, Anne Deslattes Mays, Richie Huynh, Robert J Rossi, Te-Chia Wu, Karolina Palucka, Olga Anczukow, Christine R Beck, Jacques F Banchereau
A comprehensive long-read isoform analysis platform and sequencing resource for breast cancer. Science advances 8 (3) (2022)
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)
Hoon Kim, Nam-Phuong Nguyen, Kristen Turner, Sihan Wu, Amit D Gujar, Jens Luebeck, Jihe Liu, Viraj Deshpande, Utkrisht Rajkumar, Sandeep Namburi, Samirkumar B Amin, Eunhee Yi, Francesca Menghi, Johannes H Schulte, Anton G Henssen, Howard Y Chang, Christine R Beck, Paul S Mischel, Vineet Bafna, Roel G W Verhaak
Extrachromosomal DNA is associated with oncogene amplification and poor outcome across multiple cancers. Nature genetics 52 (9) (2020)
Parithi Balachandran, Christine R Beck
Structural variant identification and characterization. Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 28 (1) (2020)