2018
DOI: 10.7287/peerj.preprints.27027
|View full text |Cite
Preprint
|
Sign up to set email alerts
|

Microsatellite development via next-generation sequencing in Acacia stenophylla (Fabaceae) and Duma florulenta (Polygonaceae): two ecologically important plant species of Australian dryland floodplains

Abstract: 6 7 Duma florulenta and Acacia stenophylla are two ecologically important but 8 understudied species that naturally occur on the floodplains and riverbanks of Australia's 9 arid and semi-arid river systems. This paper describes the discovery and characterization 10 of 12 and 13 polymorphic microsatellite markers for D. florulenta and A. stenophylla 11 respectively. The number of alleles per locus for D. florulenta ranged from 2-12 with an 12 average of 6.1. Across all samples, observed and expected heterozygos… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
3
0

Year Published

2019
2019
2019
2019

Publication Types

Select...
2

Relationship

2
0

Authors

Journals

citations
Cited by 2 publications
(3 citation statements)
references
References 0 publications
0
3
0
Order By: Relevance
“…All samples were genotyped using 13 microsatellite markers reported for A. stenophylla by Murray, Reid, and Wu () (Genbank accessions –). To reduce the costs by multiplexing, PCR products were labelled using M13 universal primers as outlined in Sheulke ().…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…All samples were genotyped using 13 microsatellite markers reported for A. stenophylla by Murray, Reid, and Wu () (Genbank accessions –). To reduce the costs by multiplexing, PCR products were labelled using M13 universal primers as outlined in Sheulke ().…”
Section: Methodsmentioning
confidence: 99%
“…All samples were genotyped using 13 microsatellite markers reported for A. stenophylla by Murray, Reid, and Wu (2018) A touchdown PCR program was used, which consisted of an initial denaturation step of 5 min at 94°C followed by three cycles of denaturation for 30 s at 94°C, annealing for 45 s at 60°C and elongation for 45 s at 72°C. This step was repeated for three cycles with annealing temperatures of 57 and 54°C and then for 30 cycles at an annealing temperature of 52°C.…”
Section: Genotypingmentioning
confidence: 99%
“…Samples were genotyped at 12 microsatellite loci reported for lignum by Murray, Reid, and Wu () (Genbank accession numbers –). To reduce the costs by multiplexing, PCR products were labeled using M13 universal primers as outlined in Sheulke ().…”
Section: Methodsmentioning
confidence: 99%