期刊文献+
任意字段
题名或关键词
题名
关键词
文摘
作者
第一作者
机构
刊名
分类号
参考文献
作者简介
基金资助
栏目信息

与基因组有关的几个问题的阐释

下载PDF
导出
摘要 本文对基因组、基因组学以及人类基因组计划的相关内容作了简要介绍.
作者 卜令康 卜祥通
机构地区 山东省平邑曾子学校
出处 《生物学教学》 北大核心 2015年第12期57-59,共3页 Biology Teaching
关键词 基因组 基因组学 C值悖论 人类基因组计划
分类号 G634.91 [文化科学—教育学]
  • 相关文献

参考文献3

二级参考文献95

  • 1Dewey FE, Grove ME, Pan CP, Goldstein BA, Bemstein JA, Chaib H, Merker JD, Goldfeder RL, Enns GM, David SP, Pakdaman N, Ormond KE, Caleshu C, Kingham K, Klein TE, Whirl-Carrillo M, Sakamoto K, Wheeler MT, Butte AJ, Ford JM, Boxer L, Ioannidis JP, Yeung AC, Altman RB, Assimes TL, Snyder M, Ashley EA, Quertermous T. Clinical interpretation and implications of whole-genome sequencing. JAMA, 2014, 311(10): 1035- 1045.
  • 2Lau TK, Cheung SW, Lo PSS, Pursley AN, Chan MK, Jiang F, Zhang H, Wang W, Jong LFJ, Yuen OKC, Chan HYC, Chan WSK, Choy KW. Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center. Ultrasound Obst Gyn, 2014, 43(3): 254-264.
  • 3Cirulli ET, Goldstein DB. Uncovering the roles of rare variants in common disease through whole-genome sequencing. Nat Rev Genet, 2010, 11(6): 415-425.
  • 4Rabbani B, Tekin M, Mahdieh N. The promise of whole-exome sequencing in medical genetics. J Hum Genet, 2014, 59(1): 5-15.
  • 5Gilissen C, Hehir-Kwa JY, Thung DT, van de Vorst M, van Bon BWM, Willemsen MH, Kwint M, Janssen IM, Hoischen A, Schenck A, Leach R, Klein R, Tearle R, Bo T, Pfundt R, Yntema HG, de Vries BBA, Kleefstra T, Brunner HG, Vissers LELM, Veltman JA. Genome sequencing identifies major causes of severe intellectual disability. Nature, 2014, 511 (7509): 344-347.
  • 6Egan JB, Shi CX, Tembe W, Christoforides A, Kurdoglu A, Sinari S, Middha S, Asmann Y, Schmidt J, Braggio E, Keats JJ, Fonseca R, Bergsagel PL, Craig DW, Carpten JD, Stewart AK. Whole-genome sequencing of multiple myeloma from diagnosis to plasma cell leukemia reveals genomic initiating events, evolution, and clonal tides. Blood, 2012, 120(5): 1060-1066.
  • 7Boycott KM, Vanstone MR, Bulman DE, MacKenzie AE. Rare-disease genetics in the era of next-generation sequencing: discovery to translation. Nat Rev Genet, 2013, 14(10): 681-691.
  • 8Ren SX, Fu G, Jiang XG, Zeng R, Miao YG, Xu H, Zhang YX, Xiong H, Lu G, Lu LF, Jiang HQ, Jia J, Tu YF, JiangJX, Gu WY, Zhang YQ, Cai Z, Sheng HH, Yin HF, Zhang Y, Zhu GF, Wan M, Huang HL, Qian z, Wang SY, Ma W, Yao ZJ, Shen Y, Qiang BQ, Xia QC, Guo XK, Danchin A, Girons IS, Somerville RL, Wen YM, Shi MH, Chen Z, Xu JG, Zhao GP. Unique physiological and pathogenic features of Leptospira interrogans revealed by whole- genome sequencing. Nature, 2003, 422(6934): 888-893.
  • 9Kan ZY, Zheng HC, Liu X, Li SY, Barber TD, Gong ZL, Gao H, Hao K, Willard MD, Xu JC, Hauptschein R, Rejto PA, Fernandez J, Wang G, Zhang QH, Wang B, Chen RH, Wang J, Lee NP, Zhou W, Lin Z, Peng ZY, Yi K, Chen SP, Li L, Fan XM, Yang J, Ye R, Ju J, Wang K, Estrella H, Deng SB, Wei P, Qiu M, Wulur IH, Liu JG, Ehsani ME, Zhang CS, Loboda A, Sung WK, Aggarwal A, Poon RT, Fan ST, Wang J, Hardwick J, Reinhard C, Dai H, Li YR, Luk JM, Mao M. Whole-genome sequencing identifies recurrent mutations in hepatocellular carcinoma. Genome Res, 2013, 23(9): 1422-1433.
  • 10Guo GW, Sun XJ, Chen C, Wu S, Huang PD, Li ZS, Dean M, Huang Y, Jia WL, Zhou Q, Tang AF, Yang ZQ, Li XX, Song PF, Zhao XK, Ye R, Zhang SQ, Lin Z, Qi MF, Wan SQ, Xie LF, Fan F, Nickerson ML, Zou XJ, Hu XD, Xing L, Lv ZJ, Mei HB, Gao S J, Liang CZ, Gao ZB, Lu JX, Yu Y, Liu CX, Li L, Fang XD, Jiang ZM, Yang J, Li CL, Zhao X, Chen J, Zhang F, Lai YQ, Lin ZG, Zhou F J, Chen H, Chan HC, Tsang S, Theodorescu D, Li YR, Zhang XQ, Wang J, Yang HM, Gui YT, Wang J, Cai ZM. Whole- genome and whole-exome sequencing of bladder cancer iden- tifies frequent alterations in genes involved in sister chr- omatid cohesion and segregation. Nat Genet, 2013, 45(12) 1459-1463.

共引文献9

生物学教学
2015年 第12期

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部