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Addressing ethical issues in H3Africa research – the views of research ethics committee members 解决非洲h3研究中的伦理问题——研究伦理委员会成员的观点
Pub Date : 2015-01-31 DOI: 10.1186/s11568-015-0006-6
J. de Vries, A. Abayomi, K. Littler, Ebony B Madden, S. McCurdy, O. Ouwe Missi Oukem-Boyer, J. Seeley, C. Staunton, G. Tangwa, P. Tindana, Jennifer Troyer
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引用次数: 44
Molecular genetics research in sub-Saharan Africa: how can the international community help? 撒哈拉以南非洲的分子遗传学研究:国际社会如何提供帮助?
Pub Date : 2014-12-01 Epub Date: 2014-09-17 DOI: 10.1186/s11568-014-0002-2
Endashaw Bekele, Walter F Bodmer, Neil Bradman, Ian W Craig, Julie Makani, Sue Povey, Charles Rotimi

Background: Opportunities provided by rapidly increasing access to educational resources, clinical and epidemiological data, DNA collections, cheaper technology and financial investment, suggest that researchers in sub-Saharan Africa outside South Africa (SSAOSA) could now join the genomics revolution on equal terms with those in the West.

Findings: Current evidence, however, suggests that, in some cases, various factors may be compromising this development. One interpretation is that urgent practical problems, which may compromise motivation, aspiration and ambition, are blocking opportunity.

Conclusions: Those wishing to help should support the SSAOSA scientists both at the level of extending collaboration networks and in stimulating academic leadership at national and institutional levels to ensure adequate resources are allocated. Members of organisations representing the international community of human geneticists, such as HUGO, have a significant responsibility in supporting such activities.

背景:快速增加的教育资源、临床和流行病学数据、DNA收集、更便宜的技术和金融投资所提供的机会表明,南非以外的撒哈拉以南非洲(SSAOSA)的研究人员现在可以与西方的研究人员平等地加入基因组学革命。研究结果:然而,目前的证据表明,在某些情况下,各种因素可能会影响这种发展。一种解释是,可能会损害动机、抱负和抱负的紧迫实际问题正在阻碍机会。结论:那些希望提供帮助的人应该在扩大合作网络和促进国家和机构层面的学术领导方面支持SSAOSA科学家,以确保分配足够的资源。代表人类遗传学家国际社会的组织成员,如HUGO,在支持此类活动方面负有重大责任。
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引用次数: 1
A whole genome analyses of genetic variants in two Kelantan Malay individuals. 两个吉兰丹马来人基因变异的全基因组分析。
Pub Date : 2014-12-01 Epub Date: 2014-10-21 DOI: 10.1186/s11568-014-0004-0
Wan Khairunnisa Wan Juhari, Nur Aida Md Tamrin, Mohd Hanif Ridzuan Mat Daud, Hatin Wan Isa, Nurfazreen Mohd Nasir, Sathiya Maran, Nur Shafawati Abdul Rajab, Khairul Bariah Ahmad Amin Noordin, Nik Norliza Nik Hassan, Rick Tearle, Rozaimi Razali, Amir Feisal Merican, Bin Alwi Zilfalil

Background: The sequencing of two members of the Royal Kelantan Malay family genomes will provide insights on the Kelantan Malay whole genome sequences. The two Kelantan Malay genomes were analyzed for the SNP markers associated with thalassemia and Helicobacter pylori infection. Helicobacter pylori infection was reported to be low prevalence in the north-east as compared to the west coast of the Peninsular Malaysia and beta-thalassemia was known to be one of the most common inherited and genetic disorder in Malaysia.

Result: By combining SNP information from literatures, GWAS study and NCBI ClinVar, 18 unique SNPs were selected for further analysis. From these 18 SNPs, 10 SNPs came from previous study of Helicobacter pylori infection among Malay patients, 6 SNPs were from NCBI ClinVar and 2 SNPs from GWAS studies. The analysis reveals that both Royal Kelantan Malay genomes shared all the 10 SNPs identified by Maran (Single Nucleotide Polymorphims (SNPs) genotypic profiling of Malay patients with and without Helicobacter pylori infection in Kelantan, 2011) and one SNP from GWAS study. In addition, the analysis also reveals that both Royal Kelantan Malay genomes shared 3 SNP markers; HBG1 (rs1061234), HBB (rs1609812) and BCL11A (rs766432) where all three markers were associated with beta-thalassemia.

Conclusions: Our findings suggest that the Royal Kelantan Malays carry the SNPs which are associated with protection to Helicobacter pylori infection. In addition they also carry SNPs which are associated with beta-thalassemia. These findings are in line with the findings by other researchers who conducted studies on thalassemia and Helicobacter pylori infection in the non-royal Malay population.

背景:对皇家吉兰丹马来家族的两个成员的基因组测序将提供吉兰丹马来人全基因组序列的见解。分析两个吉兰丹马来人基因组与地中海贫血和幽门螺杆菌感染相关的SNP标记。据报道,与马来西亚半岛西海岸相比,东北地区幽门螺杆菌感染的流行率较低,而已知-地中海贫血是马来西亚最常见的遗传和遗传疾病之一。结果:结合文献、GWAS研究和NCBI ClinVar的SNP信息,筛选出18个独特的SNP进行进一步分析。在这18个snp中,10个snp来自马来患者幽门螺杆菌感染的先前研究,6个snp来自NCBI ClinVar, 2个snp来自GWAS研究。分析显示,两个皇家吉兰丹马来基因组共享Maran(2011年吉兰丹有和没有幽门螺杆菌感染的马来患者的单核苷酸多态性(SNP)基因型分析)鉴定的所有10个SNP和GWAS研究中的1个SNP。此外,分析还显示,两个皇家吉兰丹马来基因组共有3个SNP标记;HBG1 (rs1061234), HBB (rs1609812)和BCL11A (rs766432),其中所有三种标记都与-地中海贫血相关。结论:我们的研究结果表明皇家吉兰丹马来人携带与保护幽门螺杆菌感染相关的snp。此外,它们还携带与-地中海贫血相关的snp。这些发现与其他研究人员在非皇室马来人口中进行地中海贫血和幽门螺杆菌感染研究的结果一致。
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引用次数: 4
A genome wide pattern of population structure and admixture in peninsular Malaysia Malays. 马来半岛马来人族群结构与杂合的全基因组模式。
Pub Date : 2014-12-01 Epub Date: 2014-10-30 DOI: 10.1186/s11568-014-0005-z
Wan Isa Hatin, Ab Rajab Nur-Shafawati, Ali Etemad, Wenfei Jin, Pengfei Qin, Shuhua Xu, Li Jin, Soon-Guan Tan, Pornprot Limprasert, Merican Amir Feisal, Mohammed Rizman-Idid, Bin Alwi Zilfalil

Background: The Malays consist of various sub-ethnic groups which are believed to have different ancestral origins based on their migrations centuries ago. The sub-ethnic groups can be divided based on the region they inhabit; the northern (Melayu Kedah and Melayu Kelantan), western (Melayu Minang) and southern parts (Melayu Bugis and Melayu Jawa) of Peninsular Malaysia. We analyzed 54,794 autosomal single nucleotide polymorphisms (SNPs) which were shared by 472 unrelated individuals from 17 populations to determine the genetic structure and distributions of the ancestral genetic components in five Malay sub-ethnic groups namely Melayu Bugis, Melayu Jawa, Melayu Minang, Melayu Kedah, and Melayu Kelantan. We also have included in the analysis 12 other study populations from Thailand, Indonesia, China, India, Africa and Orang Asli sub-groups in Malay Peninsula, obtained from the Pan Asian SNP Initiative (PASNPI) Consortium and International HapMap project database.

Results: We found evidence of genetic influx from Indians to Malays, more in Melayu Kedah and Melayu Kelantan which are genetically different from the other Malay sub-ethnic groups, but similar to Thai Pattani. More than 98% of these northern Malays haplotypes could be found in either Indians or Chinese populations, indicating a highly admixture pattern among populations. Nevertheless, the ancestry lines of Malays, Indonesians and Thais were traced back to have shared a common ancestor with the Proto-Malays and Chinese.

Conclusions: These results support genetic admixtures in the Peninsular Malaysia Malay populations and provided valuable information on the enigmatic demographical history as well as shed some insights into the origins of the Malays in the Malay Peninsula.

背景:马来人由不同的亚民族组成,据信他们在几个世纪前的移民中有不同的祖先起源。亚民族可以根据他们居住的地区进行划分;马来西亚半岛的北部(吉打州和吉兰丹州),西部(米南州)和南部(武吉士和爪哇)。我们分析了来自17个种群的472个无亲缘关系个体共有的54,794个常染色体单核苷酸多态性(snp),以确定马来人5个亚族群(即马来人Bugis、马来人Jawa、马来人Minang、马来人Kedah和马来人吉兰丹)祖先遗传成分的遗传结构和分布。我们还纳入了来自泰国、印度尼西亚、中国、印度、非洲和马来半岛原住民亚群的其他12个研究人群的分析,这些研究人群来自泛亚SNP倡议(PASNPI)联盟和国际HapMap项目数据库。结果:我们发现了从印度人到马来人的基因涌入的证据,更多的是在吉打州和吉兰丹州,这两个地区的基因与其他马来亚族群不同,但与泰国北大人相似。超过98%的北马来人单倍型可以在印度或中国人群中找到,这表明人群之间存在高度混合的模式。然而,马来人、印度尼西亚人和泰国人的祖先可以追溯到与原始马来人和中国人有共同的祖先。结论:这些结果支持马来西亚半岛马来人种群的遗传混合,并为神秘的人口历史提供了有价值的信息,同时也为马来半岛马来人的起源提供了一些见解。
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引用次数: 35
International code of conduct for genomic and health-related data sharing. 基因组和健康相关数据共享国际行为准则。
Pub Date : 2014-12-01 Epub Date: 2014-06-14 DOI: 10.1186/1877-6566-8-1
Sumio Sugano
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引用次数: 0
Framework for responsible sharing of genomic and health-related data. 负责任地共享基因组和健康相关数据的框架。
Pub Date : 2014-12-01 Epub Date: 2014-10-17 DOI: 10.1186/s11568-014-0003-1
Bartha Maria Knoppers
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引用次数: 215
The extent of functionality in the human genome 人类基因组的功能范围
Pub Date : 2013-07-15 DOI: 10.1186/1877-6566-7-2
J. Mattick, M. Dinger
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引用次数: 35
An economic perspective on personalized medicine 个体化医疗的经济学视角
Pub Date : 2013-04-19 DOI: 10.1186/1877-6566-7-1
Sairamesh Jakka, M. Rossbach
{"title":"An economic perspective on personalized medicine","authors":"Sairamesh Jakka, M. Rossbach","doi":"10.1186/1877-6566-7-1","DOIUrl":"https://doi.org/10.1186/1877-6566-7-1","url":null,"abstract":"","PeriodicalId":89026,"journal":{"name":"The HUGO journal","volume":"2 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2013-04-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89928192","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 71
Translational genomics in personalized medicine – scientific challenges en route to clinical practice 个性化医疗中的转化基因组学——通往临床实践的科学挑战
Pub Date : 2012-06-19 DOI: 10.1186/1877-6566-6-2
Marta Garcia Martinez de Lecea, M. Rossbach
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引用次数: 13
Current and emerging therapeutic strategies for Fanconi anemia 范可尼贫血当前和新出现的治疗策略
Pub Date : 2012-03-09 DOI: 10.1186/1877-6566-6-1
P. Shukla, K. Ghosh, B. Vundinti
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引用次数: 17
期刊
The HUGO journal
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