2004
DOI: 10.1139/x03-283
|View full text |Cite
|
Sign up to set email alerts
|

Abstract: Microsatellites or simple sequence repeats (SSRs) are highly polymorphic, codominant markers that have great value for the construction of genetic maps, comparative mapping, population genetic surveys, and paternity analyses. Here, we report the development and testing of a set of SSR markers derived from shotgun sequencing from Populus trichocarpa Torr. & A. Gray, a nonenriched genomic DNA library, and bacterial artificial chromosomes. Approximately 23% of the 1536 genomic clones and 48% of the 768 bacter… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

7
129
0

Year Published

2004
2004
2021
2021

Publication Types

Select...
10

Relationship

0
10

Authors

Journals

citations
Cited by 150 publications
(136 citation statements)
references
References 36 publications
7
129
0
Order By: Relevance
“…We chose 24 SSR loci (Supplementary Table 1) from a publically available list identified by the Populus trichocarpa Genome Project (Tuskan et al, 2004; http://www.ornl.gov/sci/ipgc/ssr_resource.htm). These loci have reliable repeat motifs, most are tri-or tetranucleotide repeats, are easily amplified, and are distributed throughout the genome.…”
Section: Pcr and Sequencing Methodsmentioning
confidence: 99%
“…We chose 24 SSR loci (Supplementary Table 1) from a publically available list identified by the Populus trichocarpa Genome Project (Tuskan et al, 2004; http://www.ornl.gov/sci/ipgc/ssr_resource.htm). These loci have reliable repeat motifs, most are tri-or tetranucleotide repeats, are easily amplified, and are distributed throughout the genome.…”
Section: Pcr and Sequencing Methodsmentioning
confidence: 99%
“…A set of 16 nuclear microsatellite markers (nSSRs) developed by van der Schoot et al (2000) and Tuskan et al (2004) and available at http://web.ornl.gov/sci/ipgc/ssr_resource.htm was used in the genotyping procedure as described in Dering et al (2015) ( Table 2). INEst 1.0 (Chybicki and Burczyk 2009) was used to estimate genetic diversity parameters at the genet level in both sexes: expected (H e ) and observed heterozygosity (H o ), number of alleles per locus (A), inbreeding coefficient of Weir and Cockerham (1984) (F IS ), and frequency of null alleles.…”
Section: Dna Extraction Genotyping and Genetic Diversitymentioning
confidence: 99%
“…We required that primers have an 80% or greater match over 70% of their length, and that they be correctly oriented and separated by the distance expected, based on the size of the products amplified. (Stirling et al, 2001) and SSR ( Tuskan et al, 2004b) Number of loci amplified with primers in family 13. Only one locus was mapped to the rust-resistance regions for each primer set.…”
Section: Construction Of Sequence Scaffoldsmentioning
confidence: 99%