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of 5
pro vyhledávání: '"Sanjaya, Prima"'
Autor:
Sanjaya, Prima1,2,3 (AUTHOR), Maljanen, Katri1,2,3 (AUTHOR), Katainen, Riku1,2,3,4 (AUTHOR), Waszak, Sebastian M.5,6,7 (AUTHOR), Ambrose, J. C. (AUTHOR), Arumugam, P. (AUTHOR), Bevers, R. (AUTHOR), Bleda, M. (AUTHOR), Boardman-Pretty, F. (AUTHOR), Boustred, C. R. (AUTHOR), Brittain, H. (AUTHOR), Brown, M. A. (AUTHOR), Caulfield, M. J. (AUTHOR), Chan, G. C. (AUTHOR), Giess, A. (AUTHOR), Griffin, J. N. (AUTHOR), Hamblin, A. (AUTHOR), Henderson, S. (AUTHOR), Hubbard, T. J. P. (AUTHOR), Jackson, R. (AUTHOR)
Publikováno v:
Genome Medicine. 7/7/2023, Vol. 15 Issue 1, p1-18. 18p.
Autor:
Sanjaya, Prima, Maljanen, Katri, Katainen, Riku, Waszak, Sebastian M., Aaltonen, Lauri A., Stegle, Oliver, Korbel, Jan O., Pitkänen, Esa
Additional file 3. The Genomics England Research Consortium.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a79d9911f9477e6463fe562cb98267e
Autor:
Sanjaya, Prima, Maljanen, Katri, Katainen, Riku, Waszak, Sebastian M., Aaltonen, Lauri A., Stegle, Oliver, Korbel, Jan O., Pitkänen, Esa
Additional file 2: Figure S1. Architecture of MuAt. Figure S2. Top-1, top-3 and top-5 accuracy, precision, recall and F1 scores of MuAt models trained with different mutation types in PCAWG and TCGA data. Figure S3. Transfer learning performance. Fig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0379823d875099c510a8f957819e6ada
Akademický článek
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Autor:
Sanjaya, Prima, Maljanen, Katri, Katainen, Riku, Waszak, Sebastian Martin, Ambrose, J. C., Arumugam, P., Bevers, R., Bleda, M., Boardman-Pretty, F., Boustred, C. R., Brittain, H., Brown, M. A., Caulfield, M. J., Chan, G. C., Giess, A., Griffin, J. N., Hamblin, A., Henderson, S., Hubbard, T. J. P., Jackson, R., Jones, L. J., Kasperaviciute, D., Kayikci, M., Kousathanas, A., Lahnstein, L., Lakey, A., Leigh, S. E. A., Leong, I. U. S., Leong, F. J., Maleady-Crowe, F., McEntagart, M., Minneci, F., Mitchell, J., Moutsianas, L., Mueller, M., Murugaesu, N., Need, A. C., O’Donovan, P., Odhams, C. A., Patch, C., Perez-Gil, D., Perez-Gil, M. B., Pullinger, J., Rahim, T., Rendon, A., Rogers, T., Savage, K., Sawant, K., Scott, R. H., Siddiq, A., Smith, S. C., Sosinsky, A., Stuckey, A., Tanguy, M., Taylor Tavares, A. L., Thomas, E. R. A., Thompson, S. R., Tucci, A., Welland, M. J., Williams, E., Witkowska, K., Wood, S. M., Zarowiecki, M., Aaltonen, Lauri A., Stegle, Oliver, Korbel, Jan O., Pitkänen, Esa
Background: Cancer genome sequencing enables accurate classification of tumours and tumour subtypes. However, prediction performance is still limited using exome-only sequencing and for tumour types with low somatic mutation burden such as many paedi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______185::f9f0a3e9ba4222be8a81d93a7e0a283b
https://infoscience.epfl.ch/record/303496
https://infoscience.epfl.ch/record/303496