2015
DOI: 10.1093/nar/gkv1179
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Gramene 2016: comparative plant genomics and pathway resources

Abstract: Gramene (http://www.gramene.org) is an online resource for comparative functional genomics in crops and model plant species. Its two main frameworks are genomes (collaboration with Ensembl Plants) and pathways (The Plant Reactome and archival BioCyc databases). Since our last NAR update, the database website adopted a new Drupal management platform. The genomes section features 39 fully assembled reference genomes that are integrated using ontology-based annotation and comparative analyses, and accessed throug… Show more

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Cited by 124 publications
(95 citation statements)
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“…Identification of enzymes involved in N uptake and utilization were retrieved from the SorghumCyc (Tello-Ruiz et al, 2016) and Kyoto Encyclopedia of Genes and Genomes (KEGG) online sorghum pathway database (Kanehisa et al, 2012). Ammonium and nitrate uptake and transporter genes described by von Wittgenstein et al (2014) and Léran et al (2014) were added for analysis.…”
Section: Methodsmentioning
confidence: 99%
“…Identification of enzymes involved in N uptake and utilization were retrieved from the SorghumCyc (Tello-Ruiz et al, 2016) and Kyoto Encyclopedia of Genes and Genomes (KEGG) online sorghum pathway database (Kanehisa et al, 2012). Ammonium and nitrate uptake and transporter genes described by von Wittgenstein et al (2014) and Léran et al (2014) were added for analysis.…”
Section: Methodsmentioning
confidence: 99%
“…Eighty-two selected SSR markers, attributed across the genome linked with amylose content QTL traits, were used to evaluate genetic diversity among rice germplasms. Primer sequences, annealing temperature and chromosomal location information were obtained from GRAMENE database [26]. PCR was performed by using Thermal Cycler GenAtlas S machine (ASTEC Co., Ltd, Fukuoka, Japan) with a total volume of 10 µL of the mixture containing 0.5 µL of template DNA (100 ng), 1 µL of 10× PCR buffer, 0.8 µL of 25 mM MgCl 2 , 0.1 µL of 1 mM dideoxynucleotides (dNTPs), 0.5 µL of 5 µM reverse and forward primers, and 0.05 µL of 0.5 units Taq DNA polymerase.…”
Section: Pcr Amplificationmentioning
confidence: 99%
“…The best choice would have been to split them according to exon ranking [37]. However, as exon annotation was lacking (or imprecise) for most species in our datasets, we split contigs into two sets: the first 252 base pairs, corresponding to the median length of the first exon in Arabidopsis, banana and rice (Gramene database [56]), used as a proxy for the first exon, and the rest of the contig. We then estimated B on these two sets of contigs.…”
Section: Variation Along Genesmentioning
confidence: 99%