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of 5
pro vyhledávání: '"Avigail Agam"'
Autor:
Avigail Agam, Binnaz Yalcin, Amarjit Bhomra, Matthew Cubin, Caleb Webber, Christopher Holmes, Jonathan Flint, Richard Mott
Publikováno v:
PLoS ONE, Vol 5, Iss 9, p e12839 (2010)
Array comparative genomic hybridization (aCGH) to detect copy number variants (CNVs) in mammalian genomes has led to a growing awareness of the potential importance of this category of sequence variation as a cause of phenotypic variation. Yet there
Externí odkaz:
https://doaj.org/article/8e7712a66c8a497facc3a86bcb072c55
Autor:
Binnaz Yalcin, Caleb Webber, Matthew Cubin, Jonathan Flint, Amarjit Bhomra, Richard Mott, Avigail Agam, Christopher Holmes
Publikováno v:
PLoS ONE
PLoS ONE, Vol 5, Iss 9, p e12839 (2010)
PLoS ONE, 2010, 5 (9), pp.e12839. ⟨10.1371/journal.pone.0012839⟩
PLoS ONE, Vol 5, Iss 9, p e12839 (2010)
PLoS ONE, 2010, 5 (9), pp.e12839. ⟨10.1371/journal.pone.0012839⟩
International audience; Background: Array comparative genomic hybridization (aCGH) to detect copy number variants (CNVs) in mammalian genomes has led to a growing awareness of the potential importance of this category of sequence variation as a cause
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cea2f7d50691ccdb68f989cebe0adaf
https://doi.org/10.1371/journal.pone.0012839
https://doi.org/10.1371/journal.pone.0012839
Autor:
Richard Mott, Sendu Bala, Richard Durbin, Christoffer Nellåker, Wei Yuan, Bret A. Payseur, José Afonso Guerra-Assunção, Polinka Hernandez-Pliego, Leah Rae Donahue, Deborah Janowitz, Nick Furlotte, Kim Wong, Rebecca E. McIntyre, Guy Slater, Jérôme Nicod, Thomas M. Keane, Eleazar Eskin, David J. Adams, L van der Weyden, Andrew Edwards, Charles A. Steward, Chris P. Ponting, Xiangchao Gan, Michael A. White, T G Belgard, Amarjit Bhomra, Leo Goodstadt, Ian J. Jackson, Laura G. Reinholdt, Petr Danecek, Jonathan Flint, Martin Goodson, Jim Stalker, Anne Czechanski, Helen Whitley, Peter L. Oliver, Binnaz Yalcin, Ewan Birney, Andreas Heger, Avigail Agam, James Cleak
Publikováno v:
Keane, T M, Goodstadt, L, Danecek, P, White, M A, Wong, K, Yalcin, B, Heger, A, Agam, A, Slater, G, Goodson, M, Furlotte, N A, Eskin, E, Nellåker, C, Whitley, H, Cleak, J, Janowitz, D, Hernandez-Pliego, P, Edwards, A, Belgard, T G, Oliver, P L, McIntyre, R E, Bhomra, A, Nicod, J, Gan, X, Yuan, W, van der Weyden, L, Steward, C A, Bala, S, Stalker, J, Mott, R, Durbin, R, Jackson, I J, Czechanski, A, Guerra-Assunção, J A, Donahue, L R, Reinholdt, L G, Payseur, B A, Ponting, C, Birney, E, Flint, J & Adams, D J 2011, ' Mouse genomic variation and its effect on phenotypes and gene regulation ', Nature, vol. 477, no. 7364, pp. 289-94 . https://doi.org/10.1038/nature10413
Nature
Nature, 2011, 477, pp.289-294. ⟨10.1038/nature10413⟩
Nature
Nature, 2011, 477, pp.289-294. ⟨10.1038/nature10413⟩
International audience; We report genome sequences of 17 inbred strains of laboratory mice and identify almost ten times more variants than previously known. We use these genomes to explore the phylogenetic history of the laboratory mouse and to exam
Autor:
Jonathan Flint, Avigail Agam, T. Grant Belgard, Christoffer Nellåker, David J. Adams, Kim Wong, Binnaz Yalcin, Chris P. Ponting, Thomas M. Keane, Wayne N. Frankel
Publikováno v:
Genome Biology
Genome Biology, 2012, 13 (6), pp.R45. ⟨10.1186/gb-2012-13-6-r45⟩
Genome Biology, 2012, 13 (6), pp.R45. ⟨10.1186/gb-2012-13-6-r45⟩
International audience; Background: Transposable element (TE)-derived sequence dominates the landscape of mammalian genomes and can modulate gene function by dysregulating transcription and translation. Our current knowledge of TEs in laboratory mous
Autor:
Richard Mott, James Cleak, Deborah Janowitz, Jérôme Nicod, Thomas M. Keane, Helen Whitley, David J. Adams, Amarjit Bhomra, Christoffer Nellåker, Binnaz Yalcin, Martin Goodson, Rebekah Dutton, Kim Wong, Leo Goodstadt, Jonathan Flint, Avigail Agam, Polinka Hernandez-Pliego, Xiangchao Gan
Publikováno v:
Nature
Nature, 2011, 477, pp.326-329. ⟨10.1038/nature10432⟩
Nature, 2011, 477, pp.326-329. ⟨10.1038/nature10432⟩
International audience; Structural variation is widespread in mammalian genomes and is an important cause of disease, but just how abundant and important structural variants (SVs) are in shaping phenotypic variation remains unclear. Without knowing h