De novo assembly and characterization of transcriptome using Illumina paired-end sequencing and identification of CesA gene in ramie (Boehmeria nivea L. Gaud)
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2164
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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De novo assembly and characterization of transcriptome using Illumina paired-end sequencing and identification of CesA gene in ramie (Boehmeria nivea L. Gaud) ; volume:14 ; number:1 ; day:26 ; month:2 ; year:2013 ; pages:1-11 ; date:12.2013
BMC genomics ; 14, Heft 1 (26.2.2013), 1-11, 12.2013
- Creator
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Liu, Touming
- Contributor
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Zhu, SiYuan
Tang, Qingming
Chen, Ping
Yu, Yongting
Tang, Shouwei
SpringerLink (Online service)
- DOI
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10.1186/1471-2164-14-125
- URN
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urn:nbn:de:1111-2016072843821
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:54 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Liu, Touming
- Zhu, SiYuan
- Tang, Qingming
- Chen, Ping
- Yu, Yongting
- Tang, Shouwei
- SpringerLink (Online service)
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Berry-Esseen bounds of weighted kernel estimator for a nonparametric regression model based on linear process errors under a LNQD sequence
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Research on Financial Risk Evaluation and Control of Tourism Enterprises Based on Improved GA Algorithm
Retraction Note: Research on Financial Risk Evaluation and Control of Tourism Enterprises Based on Improved GA Algorithm
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Transcriptome and metabolome analysis reveals anthocyanin biosynthesis pathway associated with ramie (Boehmeria nivea (L.) Gaud.) leaf color formation
A comparative study of different methods for the determination of cadmium in various tissues of ramie (Boehmeria nivea L.)
Genome-wide association study discovered favorable single nucleotide polymorphisms and candidate genes associated with ramet number in ramie (Boehmeria nivea L.)
Creation of stable Pseudomonas aeruginosa promoter–reporter fusion mutants using linear plasmid DNA transformation
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