SNPExpress: integrated visualization of genome-wide genotypes, copy numbers and gene expression levels

by Horsman Sebastiaan, Abbas Saman, Geertsma-Kleinekoort Wendy MC, Verhaak Roel GW, Sanders Mathijs A, van der Spek Peter J, Löwenberg Bob, Valk Peter JM
Published 2008-01-01

HeatMapper: powerful combined visualization of gene expression profile correlations, genotypes, phenotypes and sample characteristics

by Moorhouse Michael J, Horsman Sebastiaan, Delwel Ruud, Bijl Maarten A, Sanders Mathijs A, Verhaak Roel GW, van der Spek Peter J, Löwenberg Bob, Valk Peter JM
Published 2006-07-01

SNPExpress: Integrated Visualization of Genome-wide Genotypes, Copy Numbers and Gene Expression Levels

by Sanders, Mathijs A, Verhaak, Roel, Geertsma-Kleinekoort, Wendy MC, Abbas, Saman, Horsman, Sebastiaan, van der Spek, Peter J, Löwenberg, Bob, Valk, Peter JM
Published 2011

Increased somatic mutation burdens in normal human cells due to defective DNA polymerases.

by Robinson, Philip S, Coorens, Tim HH, Palles, Claire, Mitchell, Emily, Abascal, Federico, Olafsson, Sigurgeir, Lee, Bernard CH, Lawson, Andrew RJ, Lee-Six, Henry, Moore, Luiza, Sanders, Mathijs A, Hewinson, James, Martin, Lynn, Pinna, Claudia MA, Galavotti, Sara, Rahbari, Raheleh, Campbell, Peter J, Martincorena, Iñigo, Tomlinson, Ian, Stratton, Michael R
Published 2021

Clonal diversification and histogenesis of malignant germ cell tumours.

by Oliver, Thomas RW, Chappell, Lia, Sanghvi, Rashesh, Deighton, Lauren, Ansari-Pour, Naser, Dentro, Stefan C, Young, Matthew D, Coorens, Tim HH, Jung, Hyunchul, Butler, Tim, Neville, Matthew DC, Leongamornlert, Daniel, Sanders, Mathijs A, Hooks, Yvette, Cagan, Alex, Mitchell, Thomas J, Cortes-Ciriano, Isidro, Warren, Anne Y, Wedge, David C, Heer, Rakesh, Coleman, Nicholas, Murray, Matthew J, Campbell, Peter J, Rahbari, Raheleh, Behjati, Sam
Published 2022

The landscape of somatic mutation in normal colorectal epithelial cells.

by Lee-Six, Henry, Olafsson, Sigurgeir, Ellis, Peter, Osborne, Robert J, Sanders, Mathijs A, Moore, Luiza, Georgakopoulos, Nikitas, Torrente, Franco, Noorani, Ayesha, Goddard, Martin, Robinson, Philip, Coorens, Tim HH, O'Neill, Laura, Alder, Christopher, Wang, Jingwei, Fitzgerald, Rebecca C, Zilbauer, Matthias, Coleman, Nicholas, Saeb-Parsy, Kourosh, Martincorena, Inigo, Campbell, Peter J, Stratton, Michael R
Published 2020

Systematic Profiling of DNMT3A Variants Reveals Protein Instability Mediated by the DCAF8 E3 Ubiquitin Ligase Adaptor.

by Huang, Yung-Hsin, Chen, Chun-Wei, Sundaramurthy, Venkatasubramaniam, Słabicki, Mikołaj, Hao, Dapeng, Watson, Caroline J, Tovy, Ayala, Reyes, Jaime M, Dakhova, Olga, Crovetti, Brielle R, Galonska, Christina, Lee, Minjung, Brunetti, Lorenzo, Zhou, Yubin, Tatton-Brown, Katrina, Huang, Yun, Cheng, Xiaodong, Meissner, Alexander, Valk, Peter JM, Van Maldergem, Lionel, Sanders, Mathijs A, Blundell, Jamie R, Li, Wei, Ebert, Benjamin L, Goodell, Margaret A
Published 2021

Somatic Evolution in Non-neoplastic IBD-Affected Colon.

by Olafsson, Sigurgeir, McIntyre, Rebecca E, Coorens, Tim, Butler, Timothy, Jung, Hyunchul, Robinson, Philip S, Lee-Six, Henry, Sanders, Mathijs A, Arestang, Kenneth, Dawson, Claire, Tripathi, Monika, Strongili, Konstantina, Hooks, Yvette, Stratton, Michael R, Parkes, Miles, Martincorena, Inigo, Raine, Tim, Campbell, Peter J, Anderson, Carl A
Published 2021

Increased somatic mutation burdens in normal human cells due to defective DNA polymerases

by Robinson, Philip S., Coorens, Tim H. H., Palles, Claire, Mitchell, Emily, Abascal, Federico, Olafsson, Sigurgeir, Lee, Bernard C. H., Lawson, Andrew R. J., Lee-Six, Henry, Moore, Luiza, Sanders, Mathijs A., Hewinson, James, Martin, Lynn, Pinna, Claudia M. A., Galavotti, Sara, Rahbari, Raheleh, Campbell, Peter J., Martincorena, Iñigo, Tomlinson, Ian, Stratton, Michael R.
Published 2021

Increased somatic mutation burdens in normal human cells due to defective DNA polymerases

by Robinson, Philip S., Coorens, Tim H. H., Palles, Claire, Mitchell, Emily, Abascal, Federico, Olafsson, Sigurgeir, Lee, Bernard C. H., Lawson, Andrew R. J., Lee-Six, Henry, Moore, Luiza, Sanders, Mathijs A., Hewinson, James, Martin, Lynn, Pinna, Claudia M. A., Galavotti, Sara, Rahbari, Raheleh, Campbell, Peter J., Martincorena, Iñigo, Tomlinson, Ian, Stratton, Michael R.
Published 2021

Clonal diversification and histogenesis of malignant germ cell tumours

by Oliver, Thomas RW, Chappell, Lia, Sanghvi, Rashesh, Deighton, Lauren, Ansari-Pour, Naser, Dentro, Stefan C, Young, Matthew D, Coorens, Tim HH, Jung, Hyunchul, Butler, Tim, Neville, Matthew DC, Leongamornlert, Daniel, Sanders, Mathijs A, Hooks, Yvette, Cagan, Alex, Mitchell, Thomas J, Cortes-Ciriano, Isidro, Warren, Anne Y, Wedge, David C, Heer, Rakesh, Coleman, Nicholas, Murray, Matthew J, Campbell, Peter J, Rahbari, Raheleh, Behjati, Sam
Published 2022

Mutational landscape of normal epithelial cells in Lynch Syndrome patients.

by Lee, Bernard CH, Robinson, Philip S, Coorens, Tim HH, Yan, Helen HN, Olafsson, Sigurgeir, Lee-Six, Henry, Sanders, Mathijs A, Siu, Hoi Cheong, Hewinson, James, Yue, Sarah SK, Tsui, Wai Yin, Chan, Annie SY, Chan, Anthony KW, Ho, Siu Lun, Campbell, Peter J, Martincorena, Inigo, Buczacki, Simon JA, Yuen, Siu Tsan, Leung, Suet Yi, Stratton, Michael R
Published 2022

Mutational landscape of normal epithelial cells in Lynch Syndrome patients.

by Lee, Bernard CH, Robinson, Philip S, Coorens, Tim HH, Yan, Helen HN, Olafsson, Sigurgeir, Lee-Six, Henry, Sanders, Mathijs A, Siu, Hoi Cheong, Hewinson, James, Yue, Sarah SK, Tsui, Wai Yin, Chan, Annie SY, Chan, Anthony KW, Ho, Siu Lun, Campbell, Peter J, Martincorena, Inigo, Buczacki, Simon JA, Yuen, Siu Tsan, Leung, Suet Yi, Stratton, Michael R
Published 2022

Inherited MUTYH mutations cause elevated somatic mutation rates and distinctive mutational signatures in normal human cells.

by Robinson, Philip S, Thomas, Laura E, Abascal, Federico, Jung, Hyunchul, Harvey, Luke MR, West, Hannah D, Olafsson, Sigurgeir, Lee, Bernard CH, Coorens, Tim HH, Lee-Six, Henry, Butlin, Laura, Lander, Nicola, Truscott, Rebekah, Sanders, Mathijs A, Lensing, Stefanie V, Buczacki, Simon JA, Ten Hoopen, Rogier, Coleman, Nicholas, Brunton-Sim, Roxanne, Rushbrook, Simon, Saeb-Parsy, Kourosh, Lalloo, Fiona, Campbell, Peter J, Martincorena, Iñigo, Sampson, Julian R, Stratton, Michael R
Published 2022

Somatic mutation rates scale with lifespan across mammals.

by Cagan, Alex, Baez-Ortega, Adrian, Brzozowska, Natalia, Abascal, Federico, Coorens, Tim HH, Sanders, Mathijs A, Lawson, Andrew RJ, Harvey, Luke MR, Bhosle, Shriram, Jones, David, Alcantara, Raul E, Butler, Timothy M, Hooks, Yvette, Roberts, Kirsty, Anderson, Elizabeth, Lunn, Sharna, Flach, Edmund, Spiro, Simon, Januszczak, Inez, Wrigglesworth, Ethan, Jenkins, Hannah, Dallas, Tilly, Masters, Nic, Perkins, Matthew W, Deaville, Robert, Druce, Megan, Bogeska, Ruzhica, Milsom, Michael D, Neumann, Björn, Gorman, Frank, Constantino-Casas, Fernando, Peachey, Laura, Bochynska, Diana, Smith, Ewan St John, Gerstung, Moritz, Campbell, Peter J, Murchison, Elizabeth P, Stratton, Michael R, Martincorena, Iñigo
Published 2022

Somatic mutation rates scale with lifespan across mammals.

by Cagan, Alex, Baez-Ortega, Adrian, Brzozowska, Natalia, Abascal, Federico, Coorens, Tim HH, Sanders, Mathijs A, Lawson, Andrew RJ, Harvey, Luke MR, Bhosle, Shriram, Jones, David, Alcantara, Raul E, Butler, Timothy M, Hooks, Yvette, Roberts, Kirsty, Anderson, Elizabeth, Lunn, Sharna, Flach, Edmund, Spiro, Simon, Januszczak, Inez, Wrigglesworth, Ethan, Jenkins, Hannah, Dallas, Tilly, Masters, Nic, Perkins, Matthew W, Deaville, Robert, Druce, Megan, Bogeska, Ruzhica, Milsom, Michael D, Neumann, Björn, Gorman, Frank, Constantino-Casas, Fernando, Peachey, Laura, Bochynska, Diana, Smith, Ewan, Gerstung, Moritz, Campbell, Peter J, Murchison, Elizabeth, Stratton, Michael R, Martincorena, Iñigo
Published 2022

Inherited MUTYH mutations cause elevated somatic mutation rates and distinctive mutational signatures in normal human cells.

by Robinson, Philip S, Thomas, Laura E, Abascal, Federico, Jung, Hyunchul, Harvey, Luke MR, West, Hannah D, Olafsson, Sigurgeir, Lee, Bernard CH, Coorens, Tim HH, Lee-Six, Henry, Butlin, Laura, Lander, Nicola, Truscott, Rebekah, Sanders, Mathijs A, Lensing, Stefanie V, Buczacki, Simon JA, Ten Hoopen, Rogier, Coleman, Nicholas, Brunton-Sim, Roxanne, Rushbrook, Simon, Saeb-Parsy, Kourosh, Lalloo, Fiona, Campbell, Peter J, Martincorena, Iñigo, Sampson, Julian R, Stratton, Michael R
Published 2022

Diverse mutational landscapes in human lymphocytes.

by Machado, Heather E, Mitchell, Emily, Øbro, Nina F, Kübler, Kirsten, Davies, Megan, Leongamornlert, Daniel, Cull, Alyssa, Maura, Francesco, Sanders, Mathijs A, Cagan, Alex TJ, McDonald, Craig, Belmonte, Miriam, Shepherd, Mairi S, Vieira Braga, Felipe A, Osborne, Robert J, Mahbubani, Krishnaa, Martincorena, Iñigo, Laurenti, Elisa, Green, Anthony R, Getz, Gad, Polak, Paz, Saeb-Parsy, Kourosh, Hodson, Daniel J, Kent, David G, Campbell, Peter J
Published 2022

Diverse mutational landscapes in human lymphocytes.

by Machado, Heather E, Mitchell, Emily, Øbro, Nina F, Kübler, Kirsten, Davies, Megan, Leongamornlert, Daniel, Cull, Alyssa, Maura, Francesco, Sanders, Mathijs A, Cagan, Alex TJ, McDonald, Craig, Belmonte, Miriam, Shepherd, Mairi S, Vieira Braga, Felipe A, Osborne, Robert J, Mahbubani, Krishnaa, Martincorena, Iñigo, Laurenti, Elisa, Green, Tony, Getz, Gad, Polak, Paz, Saeb-Parsy, Kourosh, Hodson, Daniel, Kent, David G, Campbell, Peter J
Published 2022

Convergent somatic mutations in metabolism genes in chronic liver disease.

by Ng, Stanley WK, Rouhani, Foad J, Brunner, Simon F, Brzozowska, Natalia, Aitken, Sarah J, Yang, Ming, Abascal, Federico, Moore, Luiza, Nikitopoulou, Efterpi, Chappell, Lia, Leongamornlert, Daniel, Ivovic, Aleksandra, Robinson, Philip, Butler, Timothy, Sanders, Mathijs A, Williams, Nicholas, Coorens, Tim HH, Teague, Jon, Raine, Keiran, Butler, Adam P, Hooks, Yvette, Wilson, Beverley, Birtchnell, Natalie, Naylor, Huw, Davies, Susan E, Stratton, Michael R, Martincorena, Iñigo, Rahbari, Raheleh, Frezza, Christian, Hoare, Matthew, Campbell, Peter J
Published 2021