Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Eoghan D. Harrington"'
Autor:
Jae Young Choi, Zoe N. Lye, Simon C. Groen, Xiaoguang Dai, Priyesh Rughani, Sophie Zaaijer, Eoghan D. Harrington, Sissel Juul, Michael D. Purugganan
Publikováno v:
Genome Biology, Vol 21, Iss 1, Pp 1-27 (2020)
Abstract Background The circum-basmati group of cultivated Asian rice (Oryza sativa) contains many iconic varieties and is widespread in the Indian subcontinent. Despite its economic and cultural importance, a high-quality reference genome is current
Externí odkaz:
https://doaj.org/article/684ef4ff48e74bbeb5abee60a299b41a
Autor:
Dafni A. Glinos, Garrett Garborcauskas, Paul Hoffman, Nava Ehsan, Lihua Jiang, Alper Gokden, Xiaoguang Dai, François Aguet, Kathleen L. Brown, Kiran Garimella, Tera Bowers, Maura Costello, Kristin Ardlie, Ruiqi Jian, Nathan R. Tucker, Patrick T. Ellinor, Eoghan D. Harrington, Hua Tang, Michael Snyder, Sissel Juul, Pejman Mohammadi, Daniel G. MacArthur, Tuuli Lappalainen, Beryl B. Cummings
Publikováno v:
Nature. 608:353-359
Regulation of transcript structure generates transcript diversity and plays an important role in human disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::709164f7ac2f771bdf664440b59cd9b2
https://doi.org/10.1038/s41586-022-05035-y
https://doi.org/10.1038/s41586-022-05035-y
Autor:
Edward F. DeLong, Andrew Burger, Paul Den Uyl, John Beaulaurier, Elaine Luo, Daniel J. Turner, Matthew Pendelton, Eoghan D. Harrington, John M. Eppley, Sissel Juul, Xiaoguang Dai
Publikováno v:
Genome Research. 30:437-446
Viruses are the most abundant biological entities on Earth and play key roles in host ecology, evolution, and horizontal gene transfer. Despite recent progress in viral metagenomics, the inherent genetic complexity of virus populations still poses te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::177e27d159716d81ba0ed2d1b648a1e5
https://doi.org/10.1101/gr.251686.119
https://doi.org/10.1101/gr.251686.119
Autor:
Ornob Alam, Julien F. Ayroles, Scott F. Hickey, Julie Z. Peng, Xiaoguang Dai, Sissel Juul, Priyesh Rughani, Jae Young Choi, Eoghan D. Harrington, Michael D. Purugganan, Elizabeth A. Stacy
Publikováno v:
Proceedings of the National Academy of Sciences. 118
Some of the most spectacular adaptive radiations begin with founder populations on remote islands. How genetically limited founder populations give rise to the striking phenotypic and ecological diversity characteristic of adaptive radiations is a pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd5ba08a7fc8e4ea1132b3b045d8d4fe
https://doi.org/10.1073/pnas.2023801118
https://doi.org/10.1073/pnas.2023801118
Autor:
Shalini N. Jhangiani, Chad A. Shaw, Rupa S. Kanchi, Patricia I. Bader, John Beaulaurier, V. Reid Sutton, Pawel Stankiewicz, Bo Yuan, Sissel Juul, James R. Lupski, Eoghan D. Harrington, Richard A. Gibbs, Claudia M.B. Carvalho, Neil A. Hanchard, John W. Belmont, Daniel J. Turner, Hadia Hijazi, Zeynep Coban-Akdemir, Matthew Pendleton, Sau Wai Cheung, Donna M. Muzny
Publikováno v:
Genome Medicine, Vol 11, Iss 1, Pp 1-14 (2019)
Genome Medicine
Genome Medicine
Background Intrachromosomal triplications (TRP) can contribute to disease etiology via gene dosage effects, gene disruption, position effects, or fusion gene formation. Recently, post-zygotic de novo triplications adjacent to copy-number neutral geno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f50a9f15a03ddf43a7c8a6c72793cb19
http://link.springer.com/article/10.1186/s13073-019-0633-y
http://link.springer.com/article/10.1186/s13073-019-0633-y
Autor:
Alper Gokden, Sissel Juul, Snyder M, Kiran V. Garimella, Maura Costello, Patrick T. Ellinor, Kristin G. Ardlie, Ruiqi Jian, Pejman Mohammadi, Tera Bowers, Garborcauskas G, Brown Kl, Xiaoguang Dai, Linnie Jiang, Eoghan D. Harrington, François Aguet, Glinos Da, Tuuli Lappalainen, Hua Tang, Daniel G. MacArthur, Brian J. Cummings, Nava Ehsan, Nathan R. Tucker, Paul Hoffman
SummaryRegulation of transcript structure generates transcript diversity and plays an important role in human disease. The advent of long-read sequencing technologies offers the opportunity to study the role of genetic variation in transcript structu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3720960956b2a62c1c34afb73c096c5a
https://doi.org/10.1101/2021.01.22.427687
https://doi.org/10.1101/2021.01.22.427687
Autor:
Priyesh Rughani, Elizabeth A. Stacy, Julie Z. Peng, Sissel Juul, Scott E. Hickey, Xiaoguang Dai, Jae Young Choi, Eoghan D. Harrington, Michael D. Purugganan, Julien F. Ayroles
Some of the most spectacular adaptive radiations begin with founder populations on remote islands. How genetically limited founder populations give rise to the striking phenotypic and ecological diversity characteristic of adaptive radiations is a pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1efb37a410e5d2c7b5b3fb3ff37b451
https://doi.org/10.1101/2020.11.03.354068
https://doi.org/10.1101/2020.11.03.354068
Autor:
Sissel Juul, Daniel J. Turner, John Beaulaurier, David Stoddart, Phillip James, Eoghan D. Harrington, Lynn Ly, Stuart William Reid
LamPORE™ is a rapid way of testing/screening large numbers of samples for the presence or absence of SARS-CoV-2, the virus causing COVID-19. It combines barcoded multi-target amplification, 15-minute barcoded library preparation and real-time nanop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6323937098a1740f6c865b50284c2040
https://doi.org/10.1101/2020.08.07.20161737
https://doi.org/10.1101/2020.08.07.20161737
Autor:
Daniel J. Turner, Kristen K. John, Eoghan D. Harrington, David Stoddart, Sissel Juul, Sarah E. Stahl, Mark Akeson, Aaron S. Burton, Benedict Paten, Miten Jain, Sarah L. Castro-Wallace
Publikováno v:
Genes, Vol 11, Iss 1, p 76 (2020)
Genes
Volume 11
Issue 1
Genes
Volume 11
Issue 1
The MinION sequencer has made in situ sequencing feasible in remote locations. Following our initial demonstration of its high performance off planet with Earth-prepared samples, we developed and tested an end-to-end, sample-to-sequencer process that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b32203e9e5f32da8d8e1e6d199e843dd
https://www.mdpi.com/2073-4425/11/1/76
https://www.mdpi.com/2073-4425/11/1/76
Autor:
Silvina Guijarro, Daniel J. Turner, Isabel Rueda, Keith K. Vaux, Amaia Hervás, Caroline M. Nievergelt, Stephen W. Scherer, Roser Corominas, Denis Bisson, William M. Brandler, Yan Yang, Michelle S. Maile, Shih C. Tang, Claudio Toma, Christina Corsello, Shirley Tan, Jonathan Sebat, Prateek Tandon, Joe Whitney, Maria J. Arranz, Timothy Pang, Amalio Telenti, Zhuozhi Wang, Danny Antaki, Alysson R. Muotri, J. Craig Venter, Karen Pierce, Eoghan D. Harrington, Eric Courchesne, Karen Messer, Madhusudan Gujral, Sissel Juul, Boyko Kakaradov, Oanh Hong, Morgan L. Kleiber, Bru Cormand, Timothy R. Chapman, Stephen F. Kingsmore, Gaganjot Kaur, Lilia M. Iakoucheva, Joseph G. Gleeson, Bhooma Thiruvahindrapuram
Publikováno v:
Science (New York, N.Y.), vol 360, iss 6386
Brandler, WM; Antaki, D; Gujral, M; Kleiber, ML; Whitney, J; Maile, MS; et al.(2018). Paternally inherited cis-regulatory structural variants are associated with autism. SCIENCE, 360(6386), 327-330. doi: 10.1126/science.aan2261. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/5vm6k60d
Science
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Brandler, WM; Antaki, D; Gujral, M; Kleiber, ML; Whitney, J; Maile, MS; et al.(2018). Paternally inherited cis-regulatory structural variants are associated with autism. SCIENCE, 360(6386), 327-330. doi: 10.1126/science.aan2261. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/5vm6k60d
Science
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Inherited variation contributes to autismAbout one-quarter of genetic variants that are associated with autism spectrum disorder (ASD) are due to de novo mutations in protein-coding genes. Brandleret al.wanted to determine whether changes in noncodin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ee70d7ed31915a819d2f3c7ed34e750
https://doi.org/10.1126/science.aan2261
https://doi.org/10.1126/science.aan2261