Knowledge Resource Center for Ecological Environment in Arid Area
DOI | 10.1186/1471-2164-12-317 |
Short read Illumina data for the de novo assembly of a non-model snail species transcriptome (Radix balthica, Basommatophora, Pulmonata), and a comparison of assembler performance | |
Feldmeyer, Barbara1; Wheat, Christopher W.2; Krezdorn, Nicolas3; Rotter, Bjoern3; Pfenninger, Markus1 | |
通讯作者 | Feldmeyer, Barbara |
来源期刊 | BMC GENOMICS
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ISSN | 1471-2164 |
出版年 | 2011 |
卷号 | 12 |
英文摘要 | Background: Until recently, read lengths on the Solexa/Illumina system were too short to reliably assemble transcriptomes without a reference sequence, especially for non-model organisms. However, with read lengths up to 100 nucleotides available in the current version, an assembly without reference genome should be possible. For this study we created an EST data set for the common pond snail Radix balthica by Illumina sequencing of a normalized transcriptome. Performance of three different short read assemblers was compared with respect to: the number of contigs, their length, depth of coverage, their quality in various BLAST searches and the alignment to mitochondrial genes. Results: A single sequencing run of a normalized RNA pool resulted in 16,923,850 paired end reads with median read length of 61 bases. The assemblies generated by VELVET, OASES, and SeqMan NGEN differed in the total number of contigs, contig length, the number and quality of gene hits obtained by BLAST searches against various databases, and contig performance in the mt genome comparison. While VELVET produced the highest overall number of contigs, a large fraction of these were of small size (< 200bp), and gave redundant hits in BLAST searches and the mt genome alignment. The best overall contig performance resulted from the NGEN assembly. It produced the second largest number of contigs, which on average were comparable to the OASES contigs but gave the highest number of gene hits in two out of four BLAST searches against different reference databases. A subsequent meta-assembly of the four contig sets resulted in larger contigs, less redundancy and a higher number of BLAST hits. Conclusion: Our results document the first de novo transcriptome assembly of a non-model species using Illumina sequencing data. We show that de novo transcriptome assembly using this approach yields results useful for downstream applications, in particular if a meta-assembly of contig sets is used to increase contig quality. These results highlight the ongoing need for improvements in assembly methodology. |
英文关键词 | next generation sequencing short read assembly Mollusca |
类型 | Article |
语种 | 英语 |
国家 | Germany ; Finland |
收录类别 | SCI-E |
WOS记录号 | WOS:000292251600001 |
WOS关键词 | EXPRESSED SEQUENCE TAGS ; OYSTER CRASSOSTREA-GIGAS ; GENE DISCOVERY ; ANNOTATION ; GENERATION ; GENOME ; EVOLUTION ; TREE ; TOOL |
WOS类目 | Biotechnology & Applied Microbiology ; Genetics & Heredity |
WOS研究方向 | Biotechnology & Applied Microbiology ; Genetics & Heredity |
资源类型 | 期刊论文 |
条目标识符 | http://119.78.100.177/qdio/handle/2XILL650/167445 |
作者单位 | 1.Goethe Univ Frankfurt, Biodivers & Climate Res Ctr BiK F, Mol Ecol Grp, D-60323 Frankfurt, Germany; 2.Univ Helsinki, Dept Biol & Environm Sci, FI-00014 Helsinki, Finland; 3.GenXPro, Frankfurt, Germany |
推荐引用方式 GB/T 7714 | Feldmeyer, Barbara,Wheat, Christopher W.,Krezdorn, Nicolas,et al. Short read Illumina data for the de novo assembly of a non-model snail species transcriptome (Radix balthica, Basommatophora, Pulmonata), and a comparison of assembler performance[J],2011,12. |
APA | Feldmeyer, Barbara,Wheat, Christopher W.,Krezdorn, Nicolas,Rotter, Bjoern,&Pfenninger, Markus.(2011).Short read Illumina data for the de novo assembly of a non-model snail species transcriptome (Radix balthica, Basommatophora, Pulmonata), and a comparison of assembler performance.BMC GENOMICS,12. |
MLA | Feldmeyer, Barbara,et al."Short read Illumina data for the de novo assembly of a non-model snail species transcriptome (Radix balthica, Basommatophora, Pulmonata), and a comparison of assembler performance".BMC GENOMICS 12(2011). |
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