Using RNA-Seq to assemble a rose transcriptome with more than 13,000 full-length expressed genes and to develop the WagRhSNP 68k Axiom SNP array for rose (Rosa L.).
Using RNA-Seq to assemble a rose transcriptome with more than 13,000 full-length expressed genes and to develop the WagRhSNP 68k Axiom SNP array for rose (Rosa L.).
复制标题
使用 RNA-Seq 组装具有超过 13,000 个全长表达基因的玫瑰转录组,并开发玫瑰 (Rosa L.) 的 WagRhSNP 68k Axiom SNP 阵列。
DOI:
10.3389/fpls.2015.00249
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发表时间:
2015
影响因子:
5.6
通讯作者:
Smulders MJ
中科院分区:
文献类型:
--
作者:
Koning-Boucoiran CF;Esselink GD;Vukosavljev M;van 't Westende WP;Gitonga VW;Krens FA;Voorrips RE;van de Weg WE;Schulz D;Debener T;Maliepaard C;Arens P;Smulders MJ
In order to develop a versatile and large SNP array for rose, we set out to mine ESTs from diverse sets of rose germplasm. For this RNA-Seq libraries containing about 700 million reads were generated from tetraploid cut and garden roses using Illumina paired-end sequencing, and from diploid Rosa multiflora using 454 sequencing. Separate de novo assemblies were performed in order to identify single nucleotide polymorphisms (SNPs) within and between rose varieties. SNPs among tetraploid roses were selected for constructing a genotyping array that can be employed for genetic mapping and marker-trait association discovery in breeding programs based on tetraploid germplasm, both from cut roses and from garden roses. In total 68,893 SNPs were included on the WagRhSNP Axiom array. Next, an orthology-guided assembly was performed for the construction of a non-redundant rose transcriptome database. A total of 21,740 transcripts had significant hits with orthologous genes in the strawberry (Fragaria vesca L.) genome. Of these 13,390 appeared to contain the full-length coding regions. This newly established transcriptome resource adds considerably to the currently available sequence resources for the Rosaceae family in general and the genus Rosa in particular.
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