期刊文献+

De novo transcriptome assembly of RNA-Seq reads with different strategies 被引量:4

De novo transcriptome assembly of RNA-Seq reads with different strategies
原文传递
导出
摘要 De novo transcriptome assembly is an important approach in RNA-Seq data analysis and it can help us to reconstruct the transcriptome and investigate gene expression profiles without reference genome sequences.We carried out transcriptome assemblies with two RNA-Seq datasets generated from human brain and cell line,respectively.We then determined an efficient way to yield an optimal overall assembly using three different strategies.We first assembled brain and cell line transcriptome using a single k-mer length.Next we tested a range of values of k-mer length and coverage cutoff in assembling.Lastly,we combined the assembled contigs from a range of k values to generate a final assembly.By comparing these assembly results,we found that using only one k-mer value for assembly is not enough to generate good assembly results,but combining the contigs from different k-mer values could yield longer contigs and greatly improve the overall assembly. De novo transcriptome assembly is an important approach in RNA-Seq data analysis and it can help us to reconstruct the tran- scriptome and investigate gene expression profiles without reference genome sequences. We carried out transcriptome assem- blies with two RNA-Seq datasets generated from human brain and cell line, respectively. We then determined an efficient way to yield an optimal overall assembly using three different strategies. We first assembled brain and cell line transcriptome using a single k-mer length. Next we tested a range of values of k-mer length and coverage cutoff in assembling. Lastly, we com- bined the assembled contigs from a range of k values to generate a final assembly. By comparing these assembly results, we found that using only one k-mer value for assembly is not enough to generate good assembly results, but combining the contigs from different k-mer values could yield longer contigs and greatly improve the overall assembly.
出处 《Science China(Life Sciences)》 SCIE CAS 2011年第12期1129-1133,共5页 中国科学(生命科学英文版)
基金 supported by the National Basic Research Program of China (Grant Nos. 2010CB945401, 2007CB108800) National Natural Science Foundation of China (Grant Nos. 30870575, 31071162,31000590) the Science and Technology Commission of Shanghai Municipality (Grant No. 11DZ2260300)
关键词 整体组装 RNA序列 转录组 读取 基因表达谱 基因组序列 重叠群 装配结 RNA-Seq, de novo transcriptome assembly, next generation sequencing
  • 相关文献

参考文献1

二级参考文献52

  • 1Adessi C,,Matton G,Ayala G,et al.Solid phase DNA amplification: characterisation of primer attachment and amplification mechanisms. Nucleic Acids Research . 2000
  • 2Margulies M,Egholm M,Altman WE,et al.Genome sequencing in microfabricated high-density picolitre reactors. Nature . 2005
  • 3Levene MJ,Korlach J,Turner SW,et al.Zero-mode waveguides for single-molecule analysis at high concentrations. Science . 2003
  • 4Wright T P.Factors affecting the cost of airplanes. Journal of Aeronautical Sciences . 1936
  • 5Sanger F,Coulson AR.A rapid method for determining sequences in DNA by primed synthesis with DNA polymerase. Journal of Molecular Biology . 1975
  • 6Gilbert W.DNA sequencing and gene structure. Nobel lecture . 1980
  • 7Shendure J,Mitra RD,Varma C,Church GM.Advanced sequencing technologies:methods and goals. Nature Reviews Genetics . 2004
  • 8Moore,G.Cramming more components onto integrated circuits. Electronics . 1965
  • 9Sanger,F.Sequences, sequences, and sequences. Annual Review of Biochemistry . 1988
  • 10Smith L M,Fung S,Hunkapiller M W,et al.The synthesis of oligonucleotides containing an aliphatic amino group at the5‘terminus:synthesis of fluorescent DNA primers for use in DNA sequence analysis. Nucleic Acids Research . 1985

共引文献27

同被引文献121

引证文献4

二级引证文献8

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