2019
DOI: 10.1111/pbi.13111
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Tea Plant Information Archive: a comprehensive genomics and bioinformatics platform for tea plant

Abstract: Summary Tea is the world's widely consumed nonalcohol beverage with essential economic and health benefits. Confronted with the increasing large‐scale omics‐data set particularly the genome sequence released in tea plant, the construction of a comprehensive knowledgebase is urgently needed to facilitate the utilization of these data sets towards molecular breeding. We hereby present the first integrative and specially designed web‐accessible database, Tea Plant Information Archive (TPIA; http://tpia.teaplant.o… Show more

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Cited by 213 publications
(189 citation statements)
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References 55 publications
(73 reference statements)
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“…Functional annotation revealed 57823, 40003, 34066, 11963, and 34972 unigenes with alignments to NR (non-redundant protein database), Swiss-Prot (Annotated protein sequence database), KOG (Clusters of orthologous groups for eukaryotic complete genomes), KEGG (Kyoto encyclopedia of genes and genomes) and GO (Gene ontology) databases, respectively. Selected unigenes were validated according to the tea plant genome in the Tea Plant Information Archive (TPIA) (Wei et al, 2018;Xia et al, 2019)…”
Section: Rna-seq Analysismentioning
confidence: 99%
“…Functional annotation revealed 57823, 40003, 34066, 11963, and 34972 unigenes with alignments to NR (non-redundant protein database), Swiss-Prot (Annotated protein sequence database), KOG (Clusters of orthologous groups for eukaryotic complete genomes), KEGG (Kyoto encyclopedia of genes and genomes) and GO (Gene ontology) databases, respectively. Selected unigenes were validated according to the tea plant genome in the Tea Plant Information Archive (TPIA) (Wei et al, 2018;Xia et al, 2019)…”
Section: Rna-seq Analysismentioning
confidence: 99%
“…Additionally, the 5.8S ribosomal RNA (5.8S rRNA) and U6 small nuclear RNA (U6 snRNA) were used to normalize the miRNA expression level. The relative expression levels were calculated according to the 2 −DDCt method, and all qRT-PCR primers were designed with the automated primer design tool of the Tea Plant Information Archive ( Supplementary Table S1) (Xia et al, 2019). All qRT-PCR analyses were performed with three biological replicates.…”
Section: Relative Expression Analyses Of the Selected Long Non-codingmentioning
confidence: 99%
“…By comparing our finding with some other SSR development projects performed using CandiSSR, we found a similar polymorphic genic SSRs generation rate among these different studies. For example, 497 polymorphic genic SSRs were identified in the comparison of the transcriptomes representing the northern and southern population of Parrotia subaequalis [40]; and 1663 polymorphic EST-SSRs were identified by comparing the transcriptomes of tea plant and 19 Camellia species [48]. The identified SSRs in these studies were relatively small.…”
Section: Identifying and General Profiling Of Genic Ssrs In T Mongolmentioning
confidence: 97%