Proceedings of the Critical Assessment of Massive Data Analysis conferences: CAMDA 2011 (Vienna, Austria) and CAMDA 2012 (Long Beach, CA USA)

David P. Kreil, Lanyi Hu
{"title":"Proceedings of the Critical Assessment of Massive Data Analysis conferences: CAMDA 2011 (Vienna, Austria) and CAMDA 2012 (Long Beach, CA USA)","authors":"David P. Kreil, Lanyi Hu","doi":"10.4161/SYSB.28947","DOIUrl":null,"url":null,"abstract":"CAMDA has now evolved from its origins at Duke University in the year 2000, founded by Simon Lin and Kimberly Johnson, to an international conference of renown that has been affiliated with ISMB/ECCB since the 2008 meeting in Vienna, and which is now a regular official Satellite Meeting of the ISMB Conference. Since 2011, proceedings are published Open Access in partnership with Systems Biomedicine. At the CAMDA conferences, alternative analyses of annually set Contest Datasets are discussed which have been submitted by different research teams. Selected contributions are collected in the special proceedings volume presented here, including the analyses by the teams of Sol Efroni and Djork-Arné Clevert, which were chosen as the best contributions by secret vote of the delegates of CAMDA 2011 and 2012, respectively. By design, CAMDA analysis goals and the competition are very openended, which is a distinguishing feature of the contest. CAMDA can therefore take on the most challenging data sets. Over the last few years, both complex multi-track data sets and unusually large measurement series have been featured. For CAMDA 2011, the Glioblastoma multiforme subset of The Cancer Genome Atlas (TCGA) had been identified as a particularly interesting challenge. It is unusual in that it provides publicly, for several hundred patients, profiles of gene transcript expression (435 cancer patients vs 11 controls), miRNA expression (426 tumor samples vs 10 controls), genomic DNA methylation (256 tumor samples vs a control), and copy number variation (465 tumor samples vs 430 controls, including 402 matched normals), which are complemented by a variety of clinical parameters and survival outcomes. Sometimes, additional results are available from alternative technologies/platforms. The data can be downloaded at different abstraction levels, from raw (Level 1, publicly available for some platforms) via normalized (Level 2) to processed (Level 3), also facilitating integration and participation by non-domain experts. Typical questions of interest include the investigation to what degree the integration of such large heterogeneous repositories can improve our understanding of complex biomedical questions. For the 2012 contest, a subset of the Japanese Toxicogenomics Project focusing on liver proved the most popular contest data set, containing over 21,000 arrays for rats treated with mainly human drugs and profiled using the Affymetrix RAE230_2.0 GeneChip. Expression profiles (raw and processed data) were complemented by drug information and pathology data that had been compiled by Weida Tong of the US FDA. Typical questions of interest include whether a better prediction of liver-toxicity from animal experiments can be achieved, and to what degree animal studies could be replaced by in-vitro assays. In fact, the data set sparked such interesting discussions at the conference, that it has been offered again also in the following years. As in past years, the CAMDA conferences have been graced by fantastic keynotes complementing the competition program, including presentations by Terry Speed (WEHI, Australia), John Storey (Princeton, USA), and Stefano Volinia (Ferrera, Italy) at the meeting 2011 in Vienna, while in 2012 keynote lectures by Olga Troyanskaya (Princeton) and Weida Tong (FDA) provided further stimulating insight and discussions. Some of these talks are available on the respective pages of the conference website www.camda.info. Looking forward, the CAMDA 2013 proceedings will be published shortly in this series of Special Volumes, and the Contest is open for the 2014 conference to be held at Boston, USA. On behalf of the conference co-chairs, we thank all the contributors to making the meetings such an intellectually stimulating lively exchange, which has been the foundation for the long running success of the conference. Last but not least, we thank Landes Bioscience for their long-term support of the conference.","PeriodicalId":90057,"journal":{"name":"Systems biomedicine (Austin, Tex.)","volume":"1 1","pages":"75 - 75"},"PeriodicalIF":0.0000,"publicationDate":"2013-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4161/SYSB.28947","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Systems biomedicine (Austin, Tex.)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4161/SYSB.28947","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

CAMDA has now evolved from its origins at Duke University in the year 2000, founded by Simon Lin and Kimberly Johnson, to an international conference of renown that has been affiliated with ISMB/ECCB since the 2008 meeting in Vienna, and which is now a regular official Satellite Meeting of the ISMB Conference. Since 2011, proceedings are published Open Access in partnership with Systems Biomedicine. At the CAMDA conferences, alternative analyses of annually set Contest Datasets are discussed which have been submitted by different research teams. Selected contributions are collected in the special proceedings volume presented here, including the analyses by the teams of Sol Efroni and Djork-Arné Clevert, which were chosen as the best contributions by secret vote of the delegates of CAMDA 2011 and 2012, respectively. By design, CAMDA analysis goals and the competition are very openended, which is a distinguishing feature of the contest. CAMDA can therefore take on the most challenging data sets. Over the last few years, both complex multi-track data sets and unusually large measurement series have been featured. For CAMDA 2011, the Glioblastoma multiforme subset of The Cancer Genome Atlas (TCGA) had been identified as a particularly interesting challenge. It is unusual in that it provides publicly, for several hundred patients, profiles of gene transcript expression (435 cancer patients vs 11 controls), miRNA expression (426 tumor samples vs 10 controls), genomic DNA methylation (256 tumor samples vs a control), and copy number variation (465 tumor samples vs 430 controls, including 402 matched normals), which are complemented by a variety of clinical parameters and survival outcomes. Sometimes, additional results are available from alternative technologies/platforms. The data can be downloaded at different abstraction levels, from raw (Level 1, publicly available for some platforms) via normalized (Level 2) to processed (Level 3), also facilitating integration and participation by non-domain experts. Typical questions of interest include the investigation to what degree the integration of such large heterogeneous repositories can improve our understanding of complex biomedical questions. For the 2012 contest, a subset of the Japanese Toxicogenomics Project focusing on liver proved the most popular contest data set, containing over 21,000 arrays for rats treated with mainly human drugs and profiled using the Affymetrix RAE230_2.0 GeneChip. Expression profiles (raw and processed data) were complemented by drug information and pathology data that had been compiled by Weida Tong of the US FDA. Typical questions of interest include whether a better prediction of liver-toxicity from animal experiments can be achieved, and to what degree animal studies could be replaced by in-vitro assays. In fact, the data set sparked such interesting discussions at the conference, that it has been offered again also in the following years. As in past years, the CAMDA conferences have been graced by fantastic keynotes complementing the competition program, including presentations by Terry Speed (WEHI, Australia), John Storey (Princeton, USA), and Stefano Volinia (Ferrera, Italy) at the meeting 2011 in Vienna, while in 2012 keynote lectures by Olga Troyanskaya (Princeton) and Weida Tong (FDA) provided further stimulating insight and discussions. Some of these talks are available on the respective pages of the conference website www.camda.info. Looking forward, the CAMDA 2013 proceedings will be published shortly in this series of Special Volumes, and the Contest is open for the 2014 conference to be held at Boston, USA. On behalf of the conference co-chairs, we thank all the contributors to making the meetings such an intellectually stimulating lively exchange, which has been the foundation for the long running success of the conference. Last but not least, we thank Landes Bioscience for their long-term support of the conference.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
大数据分析关键评估会议论文集:CAMDA 2011(奥地利维也纳)和CAMDA 2012(美国加州长滩)
CAMDA现在已经从2000年在杜克大学由Simon Lin和Kimberly Johnson创立的起源发展成为一个著名的国际会议,自2008年维也纳会议以来一直隶属于ISMB/ECCB,现在是ISMB会议的定期官方卫星会议。自2011年以来,会议记录与Systems Biomedicine合作开放获取。在CAMDA会议上,讨论了不同研究团队提交的每年设置的竞赛数据集的替代分析。精选的贡献收集在这里展示的特别论文集中,包括Sol Efroni和djork - arnael Clevert团队的分析,他们分别通过2011年和2012年CAMDA代表的无记名投票被选为最佳贡献。通过设计,CAMDA的分析目标和比赛都是非常开放的,这是本次比赛的一大特色。因此,CAMDA可以处理最具挑战性的数据集。在过去的几年中,复杂的多轨道数据集和异常大的测量系列都已成为特色。在CAMDA 2011中,癌症基因组图谱(TCGA)的多形性胶质母细胞瘤亚群被确定为一个特别有趣的挑战。它的不寻常之处在于,它公开提供了数百名患者的基因转录表达谱(435名癌症患者对11名对照)、miRNA表达谱(426名肿瘤样本对10名对照)、基因组DNA甲基化谱(256名肿瘤样本对1名对照)和拷贝数变异谱(465名肿瘤样本对430名对照,包括402名匹配的正常人),并辅以各种临床参数和生存结果。有时,其他技术/平台可以提供额外的结果。数据可以在不同的抽象级别上下载,从原始的(第1级,对某些平台公开可用)到规范化的(第2级)再到处理过的(第3级),这也促进了非领域专家的集成和参与。感兴趣的典型问题包括调查在多大程度上集成这些大型异构存储库可以提高我们对复杂生物医学问题的理解。在2012年的比赛中,日本毒物基因组学计划的一个专注于肝脏的分支被证明是最受欢迎的比赛数据集,其中包含21,000多个主要使用人类药物治疗的大鼠阵列,并使用Affymetrix RAE230_2.0基因芯片进行分析。表达谱(原始和处理过的数据)由美国FDA的weiida Tong编制的药物信息和病理数据补充。人们感兴趣的典型问题包括是否可以通过动物实验更好地预测肝脏毒性,以及体外实验在多大程度上可以取代动物研究。事实上,该数据集在会议上引发了如此有趣的讨论,以至于在接下来的几年里它也被再次提出。与往年一样,CAMDA会议上也有精彩的主题演讲,包括2011年在维也纳举行的会议上,Terry Speed(澳大利亚WEHI)、John Storey(美国普林斯顿)和Stefano Volinia(意大利费雷拉)的演讲,2012年Olga Troyanskaya(普林斯顿)和Weida Tong (FDA)的主题演讲提供了进一步刺激的见解和讨论。其中一些演讲可以在会议网站www.camda.info的相应页面上找到。展望未来,2013年CAMDA会议记录将很快在这一系列特别卷中出版,竞赛将在2014年在美国波士顿举行的会议上开放。我们谨代表会议的共同主席,感谢所有与会者,感谢他们使会议成为一次激发智力的生动交流,这是会议长期成功的基础。最后但并非最不重要的是,我们感谢兰德斯生物科学公司对会议的长期支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Gulf War Illness: Is there lasting damage to the endocrine-immune circuitry? Survival regression by data fusion An integrative exploratory analysis of –omics data from the ICGC cancer genomes lung adenocarcinoma study Drug-induced liver injury classification model based on in vitro human transcriptomics and in vivo rat clinical chemistry data Cross-organism toxicogenomics with group factor analysis
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1