2016
DOI: 10.1186/s12864-016-2417-8
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Comparative transcriptomics and comprehensive marker resource development in mulberry

Abstract: BackgroundHigh potential of Morus laevigata and Morus serrata has been proposed in the breeding programs for Morus sp. However, due to the lack of dense molecular markers this goal is still in its nascent stage and not yet realized. We thus, sequenced the transcriptomes of these two wild Morus species and utilized the data for marker development.ResultsWe generated 87.0 and 80.3 Mb of transcriptome data from M. laevigata and M. serrata, respectively. The transcriptomes from M. laevigata and M. serrata, were as… Show more

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Cited by 22 publications
(21 citation statements)
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“…Sequence variants (InDels, frame shift, stop gained, stop lost and non synormymous coding) that potentially have high impact on transcript/protein were predicted according to the method described by Saeed et al [49]. …”
Section: Methodsmentioning
confidence: 99%
“…Sequence variants (InDels, frame shift, stop gained, stop lost and non synormymous coding) that potentially have high impact on transcript/protein were predicted according to the method described by Saeed et al [49]. …”
Section: Methodsmentioning
confidence: 99%
“…The NCBI SRA accession for the samples is SRX504963, SRX504944, SRX504924, SRX504906 and SRX504893 for leaf, male flower, winter bud, bark and root tissue respectively. Our group has previously sequenced and submitted the raw data [ 22 , 23 , 24 ] for ML and MS with accession numbers SRX1515878 and SRX1506562 respectively. Trinity software version r20140413p1 [ 25 ] with default parameters was used to assemble the sequences of M. serrata , M. laevigata and M. notabilis .…”
Section: Methodsmentioning
confidence: 99%
“…ex Brandis and M. serrata Roxb. (Saeed et al, 2016) were assembled together, and the sequences thus obtained were used for primer designing. The primers were designed by using Primer Express 2.0 software (PE Applied Biosystems) using default parameters and checked by BLAST tool against M. notabilis genome and melting curve analysis following PCR.…”
Section: Methodsmentioning
confidence: 99%