Identification of SNP markers for inferring phylogeny in temperate bamboos ( P oaceae: B ambusoideae) using RAD sequencing

2013 ◽  
Vol 13 (5) ◽  
pp. 938-945 ◽  
Author(s):  
X. Q. Wang ◽  
L. Zhao ◽  
D. A. R. Eaton ◽  
D. Z. Li ◽  
Z. H. Guo
Keyword(s):  
BMC Genomics ◽  
2015 ◽  
Vol 16 (1) ◽  
Author(s):  
Salih Kafkas ◽  
Mortaza Khodaeiaminjan ◽  
Murat Güney ◽  
Ebru Kafkas

2017 ◽  
Author(s):  
Derrick J. Thrasher ◽  
Bronwyn G. Butcher ◽  
Leonardo Campagna ◽  
Michael S. Webster ◽  
Irby J. Lovette

AbstractInformation on genetic relationships among individuals is essential to many studies of the behavior and ecology of wild organisms. Parentage and relatedness assays based on large numbers of SNP loci hold substantial advantages over the microsatellite markers traditionally used for these purposes. We present a double-digest restriction site-associated DNA sequencing (ddRAD-seq) analysis pipeline that, as such, simultaneously achieves the SNP discovery and genotyping steps and which is optimized to return a statistically powerful set of SNP markers (typically 150-600 after stringent filtering) from large numbers of individuals (up to 240 per run). We explore the tradeoffs inherent in this approach through a set of experiments in a species with a complex social system, the variegated fairy-wren (Malurus lamberti), and further validate it in a phylogenetically broad set of other bird species. Through direct comparisons with a parallel dataset from a robust panel of highly variable microsatellite markers, we show that this ddRAD-seq approach results in substantially improved power to discriminate among potential relatives and considerably more precise estimates of relatedness coefficients. The pipeline is designed to be universally applicable to all bird species (and with minor modifications to many other taxa), to be cost- and time-efficient, and to be replicable across independent runs such that genotype data from different study periods can be combined and analyzed as field samples are accumulated.


2020 ◽  
Vol 12 (3) ◽  
pp. 423-426
Author(s):  
Si Yin ◽  
Xuemei Ding ◽  
Yuehui Yan ◽  
Lizhou Tang ◽  
Haibo Wang ◽  
...  

2013 ◽  
Vol 13 (5) ◽  
pp. 899-907 ◽  
Author(s):  
Yann X. C. Bourgeois ◽  
Emeline Lhuillier ◽  
Timothée Cézard ◽  
Joris A. M. Bertrand ◽  
Boris Delahaie ◽  
...  

2020 ◽  
Author(s):  
Nan Yang ◽  
Zhaoke Dong ◽  
Aidong Chen ◽  
Yanqiong Yin ◽  
Xiangyong Li ◽  
...  

Abstract Background The white-backed planthopper (WBPH), Sogatella furcifera (Horváth) (Hemiptera, Delphacidae), is a migratory pest of rice in Asia. Shandong Province, in northern China, is located on the migration pathway of WBPH between southern and northeast China. The potential sources of WBPH in northern China are poorly understood. We studied the sources of WBPH in Shandong Province by determining the population genetic structure of WBPH in 18 sites distributed in Shandong and in six regions of the Greater Mekong Subregion (GMS). We used mitochondrial gene and single-nucleotide polymorphism (SNP) markers (2b-RAD sequencing) for analysis.Results All of the WBPH populations studied in the seven regions had low genetic diversity. Pairwise FST values ranged from − 0.061 to 0.285, while FST based on SNP data ranged from − 0.007 to 0.009. These two molecular markers revealed that 4.40% (mtDNA) and 0.19% (SNP) genetic variation could be explained by the interpopulation variation, while the rest came from intrapopulation variation. The populations in the seven geographic regions comprised four hypothetical genetic clusters (K = 4) not associated with geographic location. Eighty-four of 129 individuals distributed across the given area were designated as recent migrants or of admixed ancestry. Although the substantial migration presented, a weak but significant correlation between genetic and geographic distances was found (r = 0.083, P = 0.004).Conclusion GMS was the main source of WBPH in Shandong, while other source populations may also exist. The genetic structure of WBPH is shaped by both migration and geographic barriers. These results help clarify the migration route and the source of WBPH in northern China.


2018 ◽  
Vol 11 (4) ◽  
pp. 423-426 ◽  
Author(s):  
Yong Gao ◽  
Si Yin ◽  
Li Zhang ◽  
Yongyan Liao ◽  
Jialing Guan ◽  
...  
Keyword(s):  

2021 ◽  
Author(s):  
Ensieh Habibi ◽  
Michael R. Miller ◽  
Daphne Gille ◽  
Leigh Sanders ◽  
Jeff Rodzen ◽  
...  

Abstract The McCloud River Redband Trout (MRRT; Oncorhynchus mykiss stonei ) is a unique subspecies of rainbow trout that inhabits the isolated Upper McCloud River of Northern California. A major threat to MRRT is introgressive hybridization with non-native rainbow trout from historical stocking and contemporary unauthorized introductions . To help address this concern, we collected RAD-sequencing data on 308 total individuals from MRRT and other California O. mykiss populations and examined population structure using Principal Component and admixture analyses. Our results are consistent with previous studies; we found that populations of MRRT in Sheepheaven, Swamp, Edson, and Moosehead creeks are nonintrogressed. Additionally, we saw no evidence of introgression in Dry Creek, and suggest further investigation to determine if it can be considered a core MRRT conservation population. Sheepheaven Creek was previously thought to be the sole historical lineage of MRRT, but our analysis identified three: Sheepheaven, Edson, and Dry creeks, all of which should be preserved. Finally, we discovered diagnostic and polymorphic SNP markers for monitoring introgression and genetic diversity in MRRT. Collectively, our results provide a valuable resource for the conservation and management of MRRT.


Author(s):  
R. Andrew King ◽  
Jamie R. Stevens

AbstractThe rivers of the Hampshire Basin, southern England contain a genetically unique group of Atlantic salmon that have suffered dramatic declines in numbers over the last 40 years. Knowledge of levels and patterns of genetic diversity is essential for effective management of these vulnerable populations. Using restriction site-associated DNA sequencing (RADseq) data, we describe the development and characterisation of a panel of 94 single nucleotide polymorphism (SNP) loci for salmon from this region and investigate their applicability and variability in both target (i.e. southern English) and non-target populations. The SNP loci will be useful for population genetic and assignment studies on Atlantic salmon within the UK and beyond.


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