期刊文献+

Value of a newly sequenced bacterial genome 被引量:7

Value of a newly sequenced bacterial genome
下载PDF
导出
摘要 Next-generation sequencing(NGS) technologies have made high-throughput sequencing available to medium- and small-size laboratories, culminating in a tidal wave of genomic information. The quantity of sequenced bacterial genomes has not only brought excitement to the field of genomics but also heightened expectations that NGS would boost antibacterial discovery and vaccine development. Although many possible drug and vaccine targets have been discovered, the success rate of genome-based analysis has remained below expectations. Furthermore, NGS has had consequences for genome quality, resulting in an exponential increase in draft(partial data) genome deposits in public databases. If no further interests are expressed for a particular bacterial genome, it is more likely that the sequencing of its genome will be limited to a draft stage, and the painstaking tasks of completing the sequencing of its genome and annotation will not be undertaken. It is important to know what is lost when we settle for a draft genome and to determine the "scientific value" of a newly sequenced genome. This review addresses the expected impact of newly sequenced genomes on antibacterial discovery and vaccinology. Also, it discusses the factors that could be leading to the increase in the number of draft deposits and the consequent loss of relevant biological information. Next-generation sequencing(NGS) technologies have made high-throughput sequencing available to medium- and small-size laboratories, culminating in a tidal wave of genomic information. The quantity of sequenced bacterial genomes has not only brought excitement to the field of genomics but also heightened expectations that NGS would boost antibacterial discovery and vaccine development. Although many possible drug and vaccine targets have been discovered, the success rate of genome-based analysis has remained below expectations. Furthermore, NGS has had consequences for genome quality, resulting in an exponential increase in draft(partial data) genome deposits in public databases. If no further interests are expressed for a particular bacterial genome, it is more likely that the sequencing of its genome will be limited to a draft stage, and the painstaking tasks of completing the sequencing of its genome and annotation will not be undertaken. It is important to know what is lost when we settle for a draft genome and to determine the "scientific value" of a newly sequenced genome. This review addresses the expected impact of newly sequenced genomes on antibacterial discovery and vaccinology. Also, it discusses the factors that could be leading to the increase in the number of draft deposits and the consequent loss of relevant biological information.
出处 《World Journal of Biological Chemistry》 CAS 2014年第2期161-168,共8页 世界生物化学杂志(英文版)(电子版)
基金 Supported by Coordenao de Aperfeioamento de Pessoal de Nível Superior(CAPES)in Brazil,processes BEX 12954-12-8 and 11517-12-3,to Barbosa EGV and Aburjaile FF
关键词 Next-generation sequencing DRAFTS PROKARYOTIC GENOMES Computational tools OMICS Next-generation sequencing Drafts Prokaryotic genomes Computational tools Omics
  • 相关文献

参考文献1

二级参考文献98

  • 1Ng, S.B., Buckingham, K.J., Lee, C., Bigham, A.W., Tabor, H.K., Dent, K.M., Huff, C.D., Shannon, P.T., Jabs, E.W., Nickerson, D.A., Shendure, J., Bamshad, M.J., 2010a. Exome sequencing identifies the cause of a mendelian disorder. Nat. Genet. 42, 30--35.
  • 2Ng, S.B., Bigham, A.W., Buckingham, K.J., Hannibal, M.C., McMillin, M.J., Gildersleeve, H.I., Beck, A.E., Tabor, H.K., Cooper, G.M., Mefford, H.C., Lee, C., Turner, E.H., Smith, J.D., Rieder, M.J., Yoshiura, K., Matsumoto, N., Ohta, T., Niikawa, N., Nickerson, D.A., Bamshad, M.J., Shendure, J., 2010b. Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome. Nat. Genet. 42. 790-793.
  • 3Ng, S.B., Turner, E.H., Robertson, P.D., Flygare, S.D., Bigham, A.W., Lee, C., Shaffer, T., Wong, M., Bhattacharjee, A., Eichler, E.E., Bamshad, M., Nickerson, D.A., Shendure, J., 2009b. Targeted capture and massively parallel sequencing of 12 human exomes. Nature 461,272-276.
  • 4Novelli, G., Predazzi, I.M., Mango, R., Romeo, E, Mehta, J.L., 2010. Role of genomics in cardiovascular medicine. World J. Cardiol. 2, 428-436.
  • 5Pettersson, E., Lundeberg, J., Ahmadian, A., 2009. Generations of sequencing technologies. Genomics 93, 105-111.
  • 6Pop, M., Salzberg, S.L., 2008. Bioinformatics challenges of new sequencing technology. Trends Genet. 24, 142--149.
  • 7Pussegoda, K.A., 2010. Exome sequencing: locating causative genes in rare disorders. Clin. Genet. 78, 32--33.
  • 8Ramensky, V., Bork, E, Sunyaev, S., 2002. Human non-synonymous SNPs: server and survey. Nucleic Acids Res. 30, 3894--3900.
  • 9Rehman, A.U., Morell, R.J., Belyantseva, I.A., Khan, S.Y., Boger, E.T. Shahzad, M., Ahmed, Z.M., Riazuddin, S., Khan, S.N., Friedman, T.B. 2010. Targeted capture and next-generation sequencing identifies C9orf75 encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79 Am. J. Hum. Genet. 86, 378--388.
  • 10Rios, J., Stein, E., Shendure, J., Hobbs, H.H., Cohen, J.C., 2010. Identification by whole-genome resequencing of gene defect responsible for severe hypercholesterolemia. Hum. Mol. Genet. 19, 4313--4318.

共引文献22

同被引文献61

引证文献7

二级引证文献26

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