21 research outputs found
Pan-cancer analysis of whole genomes
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- Weisenberger
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- Wendl M. C. z
- wf Amary
- Whalley
- Wheeler
- wi Futreal
- Wigle
- Wilkerson M. D. v
- Williams
- Wilmott
- Wilson G. W. k
- Wilson R. K. z
- Wintersinger
- Wiznerowicz
- Wolf
- Wong
- Wong
- Woo
- Wood
- Wouters
- Wright
- Wright
- Wright A. J. k
- ws Ang
- Wu
- Wu
- Wu
- wv abg
- wz Hupp
- x Eils
- x Yung
- X. abp
- X. at
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- X. cq
- X. ez
- X. ez
- X. fh
- X. fv
- X. fv
- X. fv
- X. fv
- X. k Mbabaali
- X. oi
- X. S. wd
- X. tc
- X. zv
- xb Danilova
- xb Felau
- xc Lovat
- xh Curley
- xh Fulton
- Xi
- Xia
- Xiang
- Xiong
- xo Abeshouse
- xp Benz
- xp Edwards
- xr Ghori
- xs Gundem
- Xue
- xv Luxton
- xw McDermott
- xy Visakorpi
- xz Whitaker
- Y. -E. ot
- Y. -J. k
- Y. -J. xn
- Y. abp
- Y. ae
- Y. ae
- Y. ae
- Y. ae
- Y. ai
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- Y. al
- Y. bk
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- Y. rg
- Y. rj
- Y. rm
- Y. S. jf
- Y. uz
- Y. vr
- Y. wt
- Y. yc
- ya Al-Ahmadie
- Yachida
- Yamaguchi
- Yamaguchi T. N. k
- Yamamoto
- Yamaue
- Yang
- Yang
- Yang
- Yang
- Yang
- Yao
- Yaspo
- Yates
- Yau
- yb Ally
- yd Cherniack
- yd Lai
- yd Schadendorf
- ye Auman
- ye Umbricht
- Yellapantula
- Yellapantula
- yh Bathe
- yj Baylin
- Yoon
- Yu
- Yu
- Yu
- Yuan
- Yugawa
- z ah
- Z. ej
- Z. ep
- Z. fr
- Z. hv
- Z. hy
- Z. jq
- Z. kt
- Z. oe
- Zaikova
- Zapatka
- zd Gershenwald
- Zenklusen
- Zeps
- zf Ghossein
- Zhang
- Zhang
- Zhang
- Zhang
- Zhang
- Zhang
- Zhang H. b
- Zhao
- Zheng
- Zhou
- Zhou
- Zhu
- Zhu
- zi zj
- zm Jayaseelan
- Zou
- Zou
- zt Kim
- zw Lewis
- Ó. A. th
- Ø. sk
- Publication venue
- Publication date
- 11/12/2019
- Field of study
Cancer is driven by genetic change, and the advent of massively parallel sequencing has enabled systematic documentation of this variation at the whole-genome scale(1-3). Here we report the integrative analysis of 2,658 whole-cancer genomes and their matching normal tissues across 38 tumour types from the Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium of the International Cancer Genome Consortium (ICGC) and The Cancer Genome Atlas (TCGA). We describe the generation of the PCAWG resource, facilitated by international data sharing using compute clouds. On average, cancer genomes contained 4-5 driver mutations when combining coding and non-coding genomic elements; however, in around 5% of cases no drivers were identified, suggesting that cancer driver discovery is not yet complete. Chromothripsis, in which many clustered structural variants arise in a single catastrophic event, is frequently an early event in tumour evolution; in acral melanoma, for example, these events precede most somatic point mutations and affect several cancer-associated genes simultaneously. Cancers with abnormal telomere maintenance often originate from tissues with low replicative activity and show several mechanisms of preventing telomere attrition to critical levels. Common and rare germline variants affect patterns of somatic mutation, including point mutations, structural variants and somatic retrotransposition. A collection of papers from the PCAWG Consortium describes non-coding mutations that drive cancer beyond those in the TERT promoter(4); identifies new signatures of mutational processes that cause base substitutions, small insertions and deletions and structural variation(5,6); analyses timings and patterns of tumour evolution(7); describes the diverse transcriptional consequences of somatic mutation on splicing, expression levels, fusion genes and promoter activity(8,9); and evaluates a range of more-specialized features of cancer genomes(8,10-18).Peer reviewe
Tissue-engineered products capable of enhancing wound healing
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Composite anodes for lithium-ion batteries: status and trends
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Biodegradable polymers in dental tissue engineering and regeneration
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Recent Advances in Biophysical stimulation of MSC for bone regeneration
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- Publication venue
- 'Indian Society for Education and Environment'
- Publication date
- Field of study
Recent Advances in Biophysical stimulation of MSC for bone regeneration
- Author
- Adamo L Garcia-Carde-AG.
- Alin M Li Z, Stoddart MJ, Yao S-J.
- Angle SR Sena K, Sumner DR, Virdi AS.
- Baker BM Shah RP, Huang AH, Mauck RL.
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- Bassaneze V Barauna V, Lavini-Ramos C, Kalil J, Schettert I, Miyakawa A.
- Basset C Pawluck R, Becker R.
- Bassett AL Becker RO.
- Bassett C Mitchell S, Gaston S.
- Bassett C Pawluk R, Pilla A.
- Bassett C Pilla A, Pawluk R.
- Baureus Koch CLM Sommarin M, Persson BRR, Salford LG, Eberhardt JL
- Boonrungsiman S Gentleman E, Carzaniga R, Evans ND, Mccomb DW.
- Buschmann MD Kim Y, Wong M, Frank E, Hunziker EB, Grodzinsky AJ.
- Carroll SF Buckley CT, Kelly DJ.
- Carter D Beaupre G, Giori N, Helms J.
- Ceccarelli G Bloise N, Mantelli M, Gastaldi G, Fassina L, De Angelis MGC.
- Chang K Chang WH-S, Wu M-L, and Shih C.
- Chang WH-S Chen L-T, Sun J-S, Lin F-H.
- Charoenpanich A Wall ME, Tucker CJ, Andrews DMK, Lalush DS, Dirschl DR.
- Charoenpanich A Wall ME, Tucker CJ, Andrews DMK, Lalush DS, Loboa EG.
- Chen D Zhao M, Mundy GR.
- Cheung WH Chin WC, Qin L, Leung KS.
- Cho H Seo Y-K, Yoon H-H, Kim S-C, Kim S-M, Song K-Y.
- Choi JW Choi BH, Park SH, Pai KS, Li TZ, Min BH, Park SR.
- Choi WH Choi BH, Min B-H, Park SR.
- Choi Y Lee DH, Seo Y.
- Claes L Willie B.
- Claes LE Heigele CA.
- Coulthard LR White DE, Jones DL, McDermott MF, Burchill SA.
- Creecy CM Neill CFO, Arulanandam BP, Sylvia VL, Navara CS, Bizios R.
- Crowder SW Liang Y, Rath R, Park AM, Maltais S, Pintauro PN.
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