Analysis of the Mitogen-activated protein kinase kinase 4 (MAP2K4) tumor suppressor gene in ovarian cancer

por Davis, Sally J, Choong, David YH, Ramakrishna, Manasa, Ryland, Georgina L, Campbell, Ian G, Gorringe, Kylie L
Publicado 2011

JAFFAL: detecting fusion genes with long-read transcriptome sequencing

por Davidson, Nadia M., Chen, Ying, Sadras, Teresa, Ryland, Georgina L., Blombery, Piers, Ekert, Paul G., Göke, Jonathan, Oshlack, Alicia
Publicado 2022

Inferring copy number and genotype in tumour exome data

por Amarasinghe, Kaushalya C, Li, Jason, Hunter, Sally M, Ryland, Georgina L, Cowin, Prue A, Campbell, Ian G, Halgamuge, Saman K
Publicado 2014

A simple consensus approach improves somatic mutation prediction accuracy

por Goode, David L, Hunter, Sally M, Doyle, Maria A, Ma, Tao, Rowley, Simone M, Choong, David, Ryland, Georgina L, Campbell, Ian G
Publicado 2013

ASXL1 c.1934dup;p.Gly646Trpfs*12—a true somatic alteration requiring a new approach

por Yannakou, Costas K., Jones, Kate, McBean, Michelle, Thompson, Ella R., Ryland, Georgina L., Doig, Ken, Markham, John, Westerman, David, Blombery, Piers
Publicado 2017

MicroRNA Genes and Their Target 3′-Untranslated Regions Are Infrequently Somatically Mutated in Ovarian Cancers

por Ryland, Georgina L., Bearfoot, Jennifer L., Doyle, Maria A., Boyle, Samantha E., Choong, David Y. H., Rowley, Simone M., Tothill, Richard W., Gorringe, Kylie L., Campbell, Ian G.
Publicado 2012

CONTRA: copy number analysis for targeted resequencing

por Li, Jason, Lupat, Richard, Amarasinghe, Kaushalya C., Thompson, Ella R., Doyle, Maria A., Ryland, Georgina L., Tothill, Richard W., Halgamuge, Saman K., Campbell, Ian G., Gorringe, Kylie L.
Publicado 2012

Persistence of UBTF tandem duplications in remission in acute myeloid leukaemia

por Harrop, Sean, Nguyen, Phillip C., Byrne, David, Wilson, Clarissa, Ryland, Georgina L., Nguyen, Tamia, Anderson, Mary Ann, Khaw, Seong Lin, Martin, Michelle, Tiong, Ing Soo, Sanij, Elaine, Blombery, Piers
Publicado 2023

ALLSorts: an RNA-Seq subtype classifier for B-cell acute lymphoblastic leukemia

por Schmidt, Breon, Brown, Lauren M., Ryland, Georgina L., Lonsdale, Andrew, Kosasih, Hansen J., Ludlow, Louise E., Majewski, Ian J., Blombery, Piers, Ekert, Paul G., Davidson, Nadia M., Oshlack, Alicia
Publicado 2022

Multiplexed transcriptome analysis to detect ALK, ROS1 and RET rearrangements in lung cancer

por Rogers, Toni-Maree, Arnau, Gisela Mir, Ryland, Georgina L., Huang, Stephen, Lira, Maruja E., Emmanuel, Yvette, Perez, Omar D., Irwin, Darryl, Fellowes, Andrew P., Wong, Stephen Q., Fox, Stephen B.
Publicado 2017

Loss of heterozygosity: what is it good for?

por Ryland, Georgina L., Doyle, Maria A., Goode, David, Boyle, Samantha E., Choong, David Y.H., Rowley, Simone M., Li, Jason, Bowtell, David DL, Tothill, Richard W., Campbell, Ian G., Gorringe, Kylie L.
Publicado 2015

Frequent activating STAT3 mutations and novel recurrent genomic abnormalities detected in breast implant-associated anaplastic large cell lymphoma

por Blombery, Piers, Thompson, Ella, Ryland, Georgina L., Joyce, Rachel, Byrne, David J., Khoo, Christine, Lade, Stephen, Hertzberg, Mark, Hapgood, Greg, Marlton, Paula, Deva, Anand, Lindeman, Geoffrey, Fox, Stephen, Westerman, David, Prince, Miles
Publicado 2018

Mutational landscape of mucinous ovarian carcinoma and its neoplastic precursors

por Ryland, Georgina L., Hunter, Sally M., Doyle, Maria A., Caramia, Franco, Li, Jason, Rowley, Simone M., Christie, Michael, Allan, Prue E., Stephens, Andrew N., Bowtell, David D L, Campbell, Ian G., Gorringe, Kylie L.
Publicado 2015

Erratum to: Mutational landscape of mucinous ovarian carcinoma and its neoplastic precursors

por Ryland, Georgina L., Hunter, Sally M., Doyle, Maria A., Caramia, Franco, Li, Jason, Rowley, Simone M., Christie, Michael, Allan, Prue E., Stephens, Andrew N., Bowtell, David D. L., Campbell, Ian G., Gorringe, Kylie L.
Publicado 2017

CNspector: a web-based tool for visualisation and clinical diagnosis of copy number variation from next generation sequencing

por Markham, John F., Yerneni, Satwica, Ryland, Georgina L., Leong, Huei San, Fellowes, Andrew, Thompson, Ella R., De Silva, Wasanthi, Kumar, Amit, Lupat, Richard, Li, Jason, Ellul, Jason, Fox, Stephen, Dickinson, Michael, Papenfuss, Anthony T., Blombery, Piers
Publicado 2019

Publisher Correction: CNspector: a web-based tool for visualisation and clinical diagnosis of copy number variation from next generation sequencing

por Markham, John F., Yerneni, Satwica, Ryland, Georgina L., Leong, Huei San, Fellowes, Andrew, Thompson, Ella R., De Silva, Wasanthi, Kumar, Amit, Lupat, Richard, Li, Jason, Ellul, Jason, Fox, Stephen, Dickinson, Michael, Papenfuss, Anthony T., Blombery, Piers
Publicado 2020

Exome Sequencing Identifies Rare Deleterious Mutations in DNA Repair Genes FANCC and BLM as Potential Breast Cancer Susceptibility Alleles

por Thompson, Ella R., Doyle, Maria A., Ryland, Georgina L., Rowley, Simone M., Choong, David Y. H., Tothill, Richard W., Thorne, Heather, Barnes, Daniel R., Li, Jason, Ellul, Jason, Philip, Gayle K., Antill, Yoland C., James, Paul A., Trainer, Alison H., Mitchell, Gillian, Campbell, Ian G.
Publicado 2012

Bioinformatics Pipelines for Targeted Resequencing and Whole-Exome Sequencing of Human and Mouse Genomes: A Virtual Appliance Approach for Instant Deployment

por Li, Jason, Doyle, Maria A., Saeed, Isaam, Wong, Stephen Q., Mar, Victoria, Goode, David L., Caramia, Franco, Doig, Ken, Ryland, Georgina L., Thompson, Ella R., Hunter, Sally M., Halgamuge, Saman K., Ellul, Jason, Dobrovic, Alexander, Campbell, Ian G., Papenfuss, Anthony T., McArthur, Grant A., Tothill, Richard W.
Publicado 2014

Molecular profiling of low grade serous ovarian tumours identifies novel candidate driver genes

por Hunter, Sally M., Anglesio, Michael S., Ryland, Georgina L., Sharma, Raghwa, Chiew, Yoke-Eng, Rowley, Simone M., Doyle, Maria A., Li, Jason, Gilks, C. Blake, Moss, Phillip, Allan, Prue E., Stephens, Andrew N., Huntsman, David G., deFazio, Anna, Bowtell, David D., Gorringe, Kylie L., Campbell, Ian G.
Publicado 2015

Utility of clinical comprehensive genomic characterization for diagnostic categorization in patients presenting with hypocellular bone marrow failure syndromes

por Blombery, Piers, Fox, Lucy C., Ryland, Georgina L., Thompson, Ella R., Lickiss, Jennifer, McBean, Michelle, Yerneni, Satwica, Hughes, David, Greenway, Anthea, Mechinaud, Francoise, Wood, Erica M., Lieschke, Graham J., Szer, Jeff, Barbaro, Pasquale, Roy, John, Wight, Joel, Lynch, Elly, Martyn, Melissa, Gaff, Clara, Ritchie, David
Publicado 2020