scholarly journals A high density barley microsatellite consensus map with 775 SSR loci

2007 ◽  
Vol 114 (6) ◽  
pp. 1091-1103 ◽  
Author(s):  
R. K. Varshney ◽  
T. C. Marcel ◽  
L. Ramsay ◽  
J. Russell ◽  
M. S. Röder ◽  
...  
Keyword(s):  
2013 ◽  
Vol 40 (2) ◽  
pp. 95-106 ◽  
Author(s):  
Baozhu Guo ◽  
Manish K. Pandey ◽  
Guohao He ◽  
Xinyou Zhang ◽  
Boshou Liao ◽  
...  

ABSTRACT The competitiveness of peanuts in domestic and global markets has been threatened by losses in productivity and quality that are attributed to diseases, pests, environmental stresses and allergy or food safety issues. Narrow genetic diversity and a deficiency of polymorphic DNA markers severely hindered construction of dense genetic maps and quantitative trait loci (QTL) mapping in order to deploy linked markers in marker-assisted peanut improvement. The U.S. Peanut Genome Initiative (PGI) was launched in 2004, and expanded to a global effort in 2006 to address these issues through coordination of international efforts in genome research beginning with molecular marker development and improvement of map resolution and coverage. Ultimately, a peanut genome sequencing project was launched in 2012 by the Peanut Genome Consortium (PGC). We reviewed the progress for accelerated development of peanut genomic resources in peanut, such as generation of expressed sequenced tags (ESTs) (252,832 ESTs as December 2012 in the public NCBI EST database), development of molecular markers (over 15,518 SSRs), and construction of peanut genetic linkage maps, in particular for cultivated peanut. Several consensus genetic maps have been constructed, and there are examples of recent international efforts to develop high density maps. An international reference consensus genetic map was developed recently with 897 marker loci based on 11 published mapping populations. Furthermore, a high-density integrated consensus map of cultivated peanut and wild diploid relatives also has been developed, which was enriched further with 3693 marker loci on a single map by adding information from five new genetic mapping populations to the published reference consensus map.


2006 ◽  
Vol 114 (3) ◽  
pp. 487-500 ◽  
Author(s):  
T. C. Marcel ◽  
R. K. Varshney ◽  
M. Barbieri ◽  
H. Jafary ◽  
M. J. D. de Kock ◽  
...  

2004 ◽  
Vol 109 (6) ◽  
pp. 1105-1114 ◽  
Author(s):  
Daryl J. Somers ◽  
Peter Isaac ◽  
Keith Edwards

2016 ◽  
Author(s):  
Brandon Schlautman ◽  
Giovanny Covarrubias-Pazaran ◽  
Luis Diaz-Garcia ◽  
Massmo Iorizzo ◽  
James Polashock ◽  
...  

ABSTRACTThe American cranberry (Vaccinium macrocarpon Ait.) is a recently domesticated, economically important, fruit crop with limited molecular resources. New genetic resources could accelerate genetic gain in cranberry through characterization of its genomic structure and by enabling molecular-assisted breeding strategies. To increase the availability of cranberry genomic resources, genotyping-by-sequencing (GBS) was used to discover and genotype thousands of single nucleotide polymorphisms (SNPs) within three inter-related cranberry full-sib populations. Additional simple sequence repeat (SSR) loci were added to the SNP datasets and used to construct bin maps for the parents of the populations, which were then merged to create the first high-density cranberry composite map containing 6073 markers (5437 SNPs and 636 SSRs) on 12 linkage groups (LGs) spanning 1124 cM. Interestingly, higher rates of recombination were observed in maternal than paternal gametes. The large number of markers in common (mean of 57.3) and the high degree of observed collinearity (mean Pair-wise Spearman Rank Correlations > 0.99) between the LGs of the parental maps demonstrates the utility of GBS in cranberry for identifying polymorphic SNP loci that are transferable between pedigrees and populations in future trait-association studies. Furthermore, the high-density of markers anchored within the component maps allowed identification of segregation distortion regions, placement of centromeres on each of the 12 LGs, and anchoring of genomic scaffolds. Collectively, the results represent an important contribution to the current understanding of cranberry genomic structure and to the availability of molecular tools for future genetic research and breeding efforts in cranberry.


BMC Genomics ◽  
2006 ◽  
Vol 7 (1) ◽  
Author(s):  
Peter Wenzl ◽  
Haobing Li ◽  
Jason Carling ◽  
Meixue Zhou ◽  
Harsh Raman ◽  
...  

2014 ◽  
Vol 13 (5) ◽  
pp. 648-663 ◽  
Author(s):  
Marco Maccaferri ◽  
Andrea Ricci ◽  
Silvio Salvi ◽  
Sara Giulia Milner ◽  
Enrico Noli ◽  
...  

2017 ◽  
Vol 10 ◽  
pp. 117863101773510 ◽  
Author(s):  
Mauricio Ulloa ◽  
Amanda M Hulse-Kemp ◽  
Luis M De Santiago ◽  
David M Stelly ◽  
John J Burke

High-density linkage maps are vital to supporting the correct placement of scaffolds and gene sequences on chromosomes and fundamental to contemporary organismal research and scientific approaches to genetic improvement, especially in paleopolyploids with exceptionally complex genomes, eg, upland cotton ( Gossypium hirsutum L., “2n = 52”). Three independently developed intraspecific upland mapping populations were analyzed to generate 3 high-density genetic linkage single-nucleotide polymorphism (SNP) maps and a consensus map using the CottonSNP63K array. The populations consisted of a previously reported F2, a recombinant inbred line (RIL), and reciprocal RIL population, from “Phytogen 72” and “Stoneville 474” cultivars. The cluster file provided 7417 genotyped SNP markers, resulting in 26 linkage groups corresponding to the 26 chromosomes (c) of the allotetraploid upland cotton (AD)1 arisen from the merging of 2 genomes (“A” Old World and “D” New World). Patterns of chromosome-specific recombination were largely consistent across mapping populations. The high-density genetic consensus map included 7244 SNP markers that spanned 3538 cM and comprised 3824 SNP bins, of which 1783 and 2041 were in the At and Dt subgenomes with 1825 and 1713 cM map lengths, respectively. Subgenome average distances were nearly identical, indicating that subgenomic differences in bin number arose due to the high numbers of SNPs on the Dt subgenome. Examination of expected recombination frequency or crossovers (COs) on the chromosomes within each population of the 2 subgenomes revealed that COs were also not affected by the SNPs or SNP bin number in these subgenomes. Comparative alignment analyses identified historical ancestral At-subgenomic translocations of c02 and c03, as well as of c04 and c05. The consensus map SNP sequences aligned with high congruency to the NBI assembly of Gossypium hirsutum. However, the genomic comparisons revealed evidence of additional unconfirmed possible duplications, inversions and translocations, and unbalance SNP sequence homology or SNP sequence/loci genomic dominance, or homeolog loci bias of the upland tetraploid At and Dt subgenomes. The alignments indicated that 364 SNP-associated previously unintegrated scaffolds can be placed in pseudochromosomes of the NBI G hirsutum assembly. This is the first intraspecific SNP genetic linkage consensus map assembled in G hirsutum with a core of reproducible mendelian SNP markers assayed on different populations and it provides further knowledge of chromosome arrangement of genic and nongenic SNPs. Together, the consensus map and RIL populations provide a synergistically useful platform for localizing and identifying agronomically important loci for improvement of the cotton crop.


PLoS ONE ◽  
2013 ◽  
Vol 8 (12) ◽  
pp. e80569 ◽  
Author(s):  
Xiaodong Wang ◽  
Hao Wang ◽  
Yan Long ◽  
Dianrong Li ◽  
Yongtai Yin ◽  
...  

PLoS ONE ◽  
2011 ◽  
Vol 6 (12) ◽  
pp. e28495 ◽  
Author(s):  
Paweł Milczarski ◽  
Hanna Bolibok-Brągoszewska ◽  
Beata Myśków ◽  
Stefan Stojałowski ◽  
Katarzyna Heller-Uszyńska ◽  
...  

2012 ◽  
Vol 125 (8) ◽  
pp. 1619-1638 ◽  
Author(s):  
Daniela Marone ◽  
Giovanni Laidò ◽  
Agata Gadaleta ◽  
Pasqualina Colasuonno ◽  
Donatella B. M. Ficco ◽  
...  
Keyword(s):  

Sign in / Sign up

Export Citation Format

Share Document