2013
DOI: 10.1371/journal.pone.0069890
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Evaluation of Genome Sequencing Quality in Selected Plant Species Using Expressed Sequence Tags

Abstract: BackgroundWith the completion of genome sequencing projects for more than 30 plant species, large volumes of genome sequences have been produced and stored in online databases. Advancements in sequencing technologies have reduced the cost and time of whole genome sequencing enabling more and more plants to be subjected to genome sequencing. Despite this, genome sequence qualities of multiple plants have not been evaluated.Methodology/Principal FindingIntegrity and accuracy were calculated to evaluate the genom… Show more

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Cited by 29 publications
(18 citation statements)
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References 74 publications
(74 reference statements)
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“…However, the number of detected mCs is an underestimation caused by the RRBS approach, the sequencing coverage, and the stringent parameters used for mC calling (SI Materials and Methods). The 71-80% mCs in the CG context was higher than reported in other plants, in which typically 40-55% mCs are in the CG context (13,22,23). The reason for this difference is unknown but may be related to the lower GC content of the M. truncatula genome (27%) compared with other plant species (32-46%) (24).…”
Section: Differential Expression Of Nodule-specific Genes Depends On Thementioning
confidence: 68%
See 1 more Smart Citation
“…However, the number of detected mCs is an underestimation caused by the RRBS approach, the sequencing coverage, and the stringent parameters used for mC calling (SI Materials and Methods). The 71-80% mCs in the CG context was higher than reported in other plants, in which typically 40-55% mCs are in the CG context (13,22,23). The reason for this difference is unknown but may be related to the lower GC content of the M. truncatula genome (27%) compared with other plant species (32-46%) (24).…”
Section: Differential Expression Of Nodule-specific Genes Depends On Thementioning
confidence: 68%
“…Nodules were chopped with a razor blade, and nuclei were obtained by a Beckman MoFlow Astrios (Beckman Coulter) cell sorter. Comparable nuclear and total cellular mRNA pools (21,22) made possible the gene expression analysis in purified nuclei that was performed with RT-qPCR on total RNA purified from nuclei with Tri-Reagent (Sigma). Methylation analysis was performed with RRBS and MeDIP on nuclear DNA purified with the DNeasy Blood and Tissue kit (Qiagen).…”
Section: Methodsmentioning
confidence: 99%
“…speltoides and Ae. tauschii, respectively) (Kilian et al, 2011;Shangguan et al, 2013). Slicing the genomes into single chromosomes provides a powerful approach to perform structural and functional genome analysis Rey et al, 2015).…”
Section: Discussionmentioning
confidence: 99%
“…Indeed, the efficiency of the assembled MF scaffolds to identify genes was actually high, providing an excellent representation of ESTs and RNA-seq reads of sugarcane datasets, proteins from different species and genes and exons from sugarcane BACs. Recently, the ratio of ESTs coverage on plant genomes was reported to be a good parameter to distinguish good and poor assemblies (Shangguan et al, 2013). By generating MF scaffolds that cover at least 3.69 the sugarcane gene space, it was possible to achieve the same amount or even more information than that covered in the sorghum MF dataset with only 19 coverage (Bedell et al, 2005).…”
Section: Discussionmentioning
confidence: 99%