On the origin of Mycobacterium ulcerans, the causative agent of Buruli ulcer
Doig, Kenneth D, Holt, Kathryn E, Fyfe, Janet A M, Lavender, Caroline J, Eddyani, Miriam, Portaels, Françoise, Yeboah-Manu, Dorothy, Pluschke, Gerd, Seemann, Torsten, Stinear, Timothy P
Published in BMC genomics (19.06.2012)
Published in BMC genomics (19.06.2012)
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Findings from precision oncology in the clinic: rare, novel variants are a significant contributor to scaling molecular diagnostics
Doig, Kenneth D, Love, Christopher G, Conway, Thomas, Seleznev, Andrei, Ma, David, Fellowes, Andrew, Blombery, Piers, Fox, Stephen B
Published in BMC medical genomics (26.03.2022)
Published in BMC medical genomics (26.03.2022)
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Canary: an atomic pipeline for clinical amplicon assays
Doig, Kenneth D, Ellul, Jason, Fellowes, Andrew, Thompson, Ella R, Ryland, Georgina, Blombery, Piers, Papenfuss, Anthony T, Fox, Stephen B
Published in BMC bioinformatics (15.12.2017)
Published in BMC bioinformatics (15.12.2017)
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Journal Article
Complete Genome Sequence of the Frog Pathogen Mycobacterium ulcerans Ecovar Liflandii
Tobias, Nicholas J, Doig, Kenneth D, Medema, Marnix H, Chen, Honglei, Haring, Volker, Moore, Robert, Seemann, Torsten, Stinear, Timothy P
Published in Journal of Bacteriology (01.02.2013)
Published in Journal of Bacteriology (01.02.2013)
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Journal Article
PathOS: a decision support system for reporting high throughput sequencing of cancers in clinical diagnostic laboratories
Doig, Kenneth D, Fellowes, Andrew, Bell, Anthony H, Seleznev, Andrei, Ma, David, Ellul, Jason, Li, Jason, Doyle, Maria A, Thompson, Ella R, Kumar, Amit, Lara, Luis, Vedururu, Ravikiran, Reid, Gareth, Conway, Thomas, Papenfuss, Anthony T, Fox, Stephen B
Published in Genome medicine (24.04.2017)
Published in Genome medicine (24.04.2017)
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Journal Article
Tumour mutational burden: an overview for pathologists
Doig, Kenneth D., Fellowes, Andrew, Scott, Prudence, Fox, Stephen B.
Published in Pathology (01.04.2022)
Published in Pathology (01.04.2022)
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Journal Article
Shariant platform: Enabling evidence sharing across Australian clinical genetic-testing laboratories to support variant interpretation
Tudini, Emma, Andrews, James, Lawrence, David M., King-Smith, Sarah L., Baker, Naomi, Baxter, Leanne, Beilby, John, Bennetts, Bruce, Beshay, Victoria, Black, Michael, Boughtwood, Tiffany F., Brion, Kristian, Cheong, Pak Leng, Christie, Michael, Christodoulou, John, Cox, Kathy, Davis, Mark R., Dejong, Lucas, Dinger, Marcel E., Doig, Kenneth D., Douglas, Evelyn, Dubowsky, Andrew, Ellul, Melissa, Fellowes, Andrew, Fisk, Katrina, Fortuno, Cristina, Friend, Kathryn, Gallagher, Renee L., Gao, Song, Hackett, Emma, Hadler, Johanna, Hipwell, Michael, Ho, Gladys, Hollway, Georgina, Hooper, Amanda J., Kassahn, Karin S., Krishnaraj, Rahul, Lau, Chiyan, Le, Huong, San Leong, Huei, Lundie, Ben, Lunke, Sebastian, Marty, Anthony, McPhillips, Mary, Nguyen, Lan T., Nones, Katia, Palmer, Kristen, Pearson, John V., Quinn, Michael C.J., Rawlings, Lesley H., Sadedin, Simon, Sanchez, Louisa, Schreiber, Andreas W., Sigalas, Emanouil, Simsek, Aygul, Soubrier, Julien, Stark, Zornitza, Thompson, Bryony A., U, James, Vakulin, Cassandra G., Wells, Amanda V., Wise, Cheryl A., Woods, Rick, Ziolkowski, Andrew, Brion, Marie-Jo, Scott, Hamish S., Thorne, Natalie P., Spurdle, Amanda B., Akesson, Lauren, Allcock, Richard, Ashton, Katie, Bell, Damon A., Brown, Anna, Buckley, Michael, Burrows, Linda, Byrne, Alicia, Chan, Eva, Cliffe, Corrina, Clifton-Bligh, Roderick, Dooley, Susan, Fernandez, Miriam Fanjul, Farnsworth, Elizabeth, Ha, Thuong, Henry, Denae, Holds, Duncan, Holman, Katherine, Jackson, Matilda, Kang, Sinlay, Luxford, Catherine, McManus, Sam, Mehrtens, Rachael, Meldrum, Cliff, Pantaleo, Sarah-Jane, Phelan, Dean, Pontikinas, Electra, Ravine, Anja, Roscioli, Tony, Scott, Rodney, Simons, Keryn, Vanwageningen, Oliver
Published in American journal of human genetics (03.11.2022)
Published in American journal of human genetics (03.11.2022)
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