2015
DOI: 10.3732/apps.1500001
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Development and characterization of EST‐SSR markers in Bombax ceiba (Malvaceae)

Abstract: Premise of the study:Bombax ceiba (Malvaceae), commonly known as silk cotton tree, is a multipurpose tree species of tropical forests. Novel expressed sequence tag–simple sequence repeat (EST-SSR) markers were developed and characterized for the species using transcriptome analysis.Methods and Results:A total of 33 new EST-SSR markers were developed for B. ceiba, of which 13 showed polymorphisms across the 24 individuals from four distant populations tested in the study. The results showed that the number of a… Show more

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Cited by 9 publications
(6 citation statements)
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“…The sequencing was carried out on HiSeq sequencing platforms at BGI‐Shenzhen (Guangdong, China). For further details on RNA extractions, transcriptome sequencing, and assembly, see Ju et al (). Then we developed primers of five species‐specific low‐copy nuclear loci (23311, 38541, 41398, 45367, and 56546) following the procedures described by Ye et al ().…”
Section: Methodsmentioning
confidence: 99%
“…The sequencing was carried out on HiSeq sequencing platforms at BGI‐Shenzhen (Guangdong, China). For further details on RNA extractions, transcriptome sequencing, and assembly, see Ju et al (). Then we developed primers of five species‐specific low‐copy nuclear loci (23311, 38541, 41398, 45367, and 56546) following the procedures described by Ye et al ().…”
Section: Methodsmentioning
confidence: 99%
“…Six highly variable pairs of EST‐SSR primers (Appendix ) were used to detected polymorphisms in B. ceiba . PCR amplification was performed according to the procedure described previously by Ju, Ma, Xin, Zhou, and Tian (). All of the high‐quality PCR products were sequenced using the amplified forward and reverse primers with an ABI 3730xl Sequence Analyzer (Life Technologies, Carlsbad, CA, USA).…”
Section: Methodsmentioning
confidence: 99%
“…TB2013079, deposited at the Herbarium of Southwest Forestry University [SWFC], Kunming, China) and immediately frozen in liquid nitrogen, and then stored at −80°C. RNA extraction, cDNA library construction, and transcriptome sequencing were conducted following the procedures previously described by Ju et al (2015). After removing adapter sequences and low-quality sequences, a total of 86,138,489 nonredundant unigenes were assembled from 95,791,418 raw reads.…”
Section: Methods and Resultsmentioning
confidence: 99%