Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Jiqiu Cheng"'
Autor:
Jiqiu Cheng, Jonas Demeulemeester, David C. Wedge, Hans Kristian M. Vollan, Jason J. Pitt, Hege G. Russnes, Bina P. Pandey, Gro Nilsen, Silje Nord, Graham R. Bignell, Kevin P. White, Anne-Lise Børresen-Dale, Peter J. Campbell, Vessela N. Kristensen, Michael R. Stratton, Ole Christian Lingjærde, Yves Moreau, Peter Van Loo
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-14 (2017)
Homozygous deletions are rare in cancers and often target tumour suppressor genes. Here, the authors conduct pan-cancer analyses and apply statistical modelling to identify 27 candidate tumour suppressors, including MAFTRR, KIAA1551, and IGF2BP2.
Externí odkaz:
https://doaj.org/article/e28c2813abff4f109325d96bafff3976
Autor:
Jiqiu Cheng, Jonas Demeulemeester, David C. Wedge, Hans Kristian M. Vollan, Jason J. Pitt, Hege G. Russnes, Bina P. Pandey, Gro Nilsen, Silje Nord, Graham R. Bignell, Kevin P. White, Anne-Lise Børresen-Dale, Peter J. Campbell, Vessela N. Kristensen, Michael R. Stratton, Ole Christian Lingjærde, Yves Moreau, Peter Van Loo
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-1 (2019)
The original version of this Article omitted a declaration from the competing interests statement, which should have included the following: ‘K.P.W. is President of Tempus Lab, Inc., Chicago, IL, USA’. This has now been corrected in both the PDF
Externí odkaz:
https://doaj.org/article/8456cf857ba94524809cf64333ad72c5
Autor:
Jiqiu Cheng, Jonas Demeulemeester, David C. Wedge, Hans Kristian M. Vollan, Jason J. Pitt, Hege G. Russnes, Bina P. Pandey, Gro Nilsen, Silje Nord, Graham R. Bignell, Kevin P. White, Anne-Lise Børresen-Dale, Peter J. Campbell, Vessela N. Kristensen, Michael R. Stratton, Ole Christian Lingjærde, Yves Moreau, Peter Van Loo
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-1 (2018)
The original version of this Article contained an error in the author affiliations. The affiliation of Kevin P. White with Tempus Labs, Inc., Chicago, IL, USA was inadvertently omitted.This has now been corrected in both the PDF and HTML versions of
Externí odkaz:
https://doaj.org/article/340c2accd0cc41b6a16ec2081ec57688
Publikováno v:
Education and Information Technologies. 27:9125-9143
Autor:
Anne Lise Børresen-Dale, Vessela N. Kristensen, Bina P. Pandey, Hans Kristian Moen Vollan, Jonas Demeulemeester, Peter J. Campbell, David C. Wedge, Graham R. Bignell, Michael R. Stratton, Yves Moreau, Silje Nord, Gro Nilsen, Jason J. Pitt, Kevin P. White, Ole Christian Lingjærde, Hege G. Russnes, Jiqiu Cheng, Peter Van Loo
Publikováno v:
Nature Communications
Nature Communications, Vol 9, Iss 1, Pp 1-1 (2018)
Nature Communications, Vol 10, Iss 1, Pp 1-1 (2019)
Nature Communications, Vol 9, Iss 1, Pp 1-1 (2018)
Nature Communications, Vol 10, Iss 1, Pp 1-1 (2019)
Homozygous deletions are rare in cancers and often target tumour suppressor genes. Here, we build a compendium of 2218 primary tumours across 12 human cancer types and systematically screen for homozygous deletions, aiming to identify rare tumour sup
Autor:
Michael R. Stratton, Gro Nilsen, Jiqiu Cheng, Anne Lise Børresen-Dale, Peter Van Loo, Jonas Demeulemeester, Peter J. Campbell, Ole Christian Lingjærde, Silje Nord, Hans Kristian Moen Vollan, Graham R. Bignell, Bina P. Pandey, Vessela N. Kristensen, David C. Wedge, Jason J. Pitt, Yves Moreau, Kevin P. White, Hege G. Russnes
Publikováno v:
Nature Communications
Nature Communications, Vol 8, Iss 1, Pp 1-14 (2017)
Cheng, J, Demeulemeester, J, Wedge, D C, Vollan, H K M, Pitt, J J, Russnes, H G, Pandey, B P, Nilsen, G, Nord, S, Bignell, G R, White, K P, Børresen-Dale, A-L, Campbell, P J, Kristensen, V N, Stratton, M R, Lingjærde, O C, Moreau, Y & Van Loo, P 2017, ' Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors ', Nature Communications . https://doi.org/10.1038/s41467-017-01355-0
Nature Communications, Vol 8, Iss 1, Pp 1-14 (2017)
Cheng, J, Demeulemeester, J, Wedge, D C, Vollan, H K M, Pitt, J J, Russnes, H G, Pandey, B P, Nilsen, G, Nord, S, Bignell, G R, White, K P, Børresen-Dale, A-L, Campbell, P J, Kristensen, V N, Stratton, M R, Lingjærde, O C, Moreau, Y & Van Loo, P 2017, ' Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors ', Nature Communications . https://doi.org/10.1038/s41467-017-01355-0
Homozygous deletions are rare in cancers and often target tumour suppressor genes. Here, we build a compendium of 2218 primary tumours across 12 human cancer types and systematically screen for homozygous deletions, aiming to identify rare tumour sup
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c125438c4afebd6d0b663bb7b26fb99
https://ora.ox.ac.uk/objects/uuid:cd270677-82f7-49d9-ae48-b99fe0fd70e7
https://ora.ox.ac.uk/objects/uuid:cd270677-82f7-49d9-ae48-b99fe0fd70e7
Autor:
Nick Telford, Nicole Dastugue, Michael R. Stratton, Paul Sinclair, Yang Li, Peter Vandenberghe, Richard J. Q. McNally, Fiona M. Ross, Patricia Jacobs, Nyla A. Heerema, Christine J. Harrison, Julian Borrow, Peter Van Loo, Olivia Joseph, Vikki Rand, Polly Talley, Philip J. Stephens, Bryan D. Young, Claire Schwab, Nick Bown, Mark Maddison, Andrew J. Carroll, Hazel M. Robinson, Anthony V. Moorman, Claudia Haferlach, Elli Papaemmanuil, Mike Griffiths, Peter J. Campbell, Lorraine Gaunt, Ben Robinson, Sarra Ryan, Sara Dyer, Manuel R. Teixeira, Jiqiu Cheng
Publikováno v:
Nature
Changes in gene dosage are a major driver of cancer, known to be caused by a finite, but increasingly well annotated, repertoire of mutational mechanisms1. This can potentially generate correlated copy-number alterations across hundreds of linked gen
Autor:
Jiqiu Cheng1 jiqiu.cheng@esat.kuleuven.be, Janssens, Steven1 Steven.Janssens@biw.kuleuven.be, Buys, Nadine1 Nadine.Buys@biw.kuleuven.be
Publikováno v:
BMC Genetics. 2009, Vol. 10, Special section p1-9. 9p. 1 Chart, 4 Graphs.
Autor:
Thierry Voet, Eric Legius, Yves Moreau, Koen Theunis, Sophie Debrock, Masoud Zamani Esteki, Karen Sermon, Martine De Rycke, Joris Vermeesch, Niels Van der Aa, Thomas D'Hooghe, Cindy Melotte, Rakhi Das, Parveen Kumar, Ligia Mateiu, Jiqiu Cheng, Eftychia Dimitriadou, Pieter Verdyck
Methods for haplotyping and DNA copy-number typing of single cells are paramount for studying genomic heterogeneity and enabling genetic diagnosis. Before analyzing the DNA of a single cell by microarray or next-generation sequencing, a whole-genome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75ea5187130b81eb0ef17c2d418be39f
https://europepmc.org/articles/PMC4473724/
https://europepmc.org/articles/PMC4473724/
Autor:
Masoud Zamani Esteki, Joris Vermeesch, Eftychia Dimitriadou, Yves Moreau, Parveen Kumar, Jiqiu Cheng, Niels Van der Aa, Ligia Mateiu, Thierry Voet, Evelyne Vanneste
Publikováno v:
Nucleic Acids Research
Single-cell genomics is revolutionizing basic genome research and clinical genetic diagnosis. However, none of the current research or clinical methods for single-cell analysis distinguishes between the analysis of a cell in G1-, S- or G2/M-phase of