Potential donor - NLR acceptor gene sets, as observed from phylogenetic trees of the donor ID genes. High bootstrap support (> 85) was used to determine likely donor ID and acceptor NLR-ID gene clades. (XLSX 28 kb
Data generated associated with understanding the features of NLRs in Arabidopsis Col-0. Contains: ...
Phylogenetic tree of Response Regulators in Arabidopsis thaliana, Cajanus cajan, Cicer arietinum, Gl...
The average neutral divergence rates of different domains in R-genes in the legume family. Note that...
Clade memberships of all NLRs present in the tree in Fig. 1 and corresponding integrated domains pr...
All NLR-IDs found in nine grasses (e-value at relaxed cut-offâ<â0.05), including the genes that ...
Bar plot of number of NLRs in each clade and percent of NLRs from each clade that overlap with predi...
The AP2b/MYB-NLR domain shuffling includes duplication of AP2 gene and inter-chromosomal transfer of...
Quality assessment of the gene datasets used for phylogenetic analysis: N50 and size of the correspo...
Locations, gene identifiers, and tandem classifications for all discovered tandem NLRs in eight gras...
The alignment of NB, ARC1, and ARC2 used to train the HMM for NLR proteins used for phylogenetic ana...
Maximum likelihood phylogeny based on the NB-ARC domain of all NLRs and NLR-IDs for each of the nine...
Manual curation of the genomic regions surrounding MIC1 genes in Brachypodium and rice. (A) MIC1 NLR...
Protein ids and corresponding domains of putative NLR-IDs from all plant species. Table of domain ar...
This Figshare project contains data for paper entitled "Dominant integration locus drives continuous...
Here we identified cell-surface (LRR-RLKs, LRR-RLPs, LysM-RLKs and LysM-RLPs) and intracellular immu...
Data generated associated with understanding the features of NLRs in Arabidopsis Col-0. Contains: ...
Phylogenetic tree of Response Regulators in Arabidopsis thaliana, Cajanus cajan, Cicer arietinum, Gl...
The average neutral divergence rates of different domains in R-genes in the legume family. Note that...
Clade memberships of all NLRs present in the tree in Fig. 1 and corresponding integrated domains pr...
All NLR-IDs found in nine grasses (e-value at relaxed cut-offâ<â0.05), including the genes that ...
Bar plot of number of NLRs in each clade and percent of NLRs from each clade that overlap with predi...
The AP2b/MYB-NLR domain shuffling includes duplication of AP2 gene and inter-chromosomal transfer of...
Quality assessment of the gene datasets used for phylogenetic analysis: N50 and size of the correspo...
Locations, gene identifiers, and tandem classifications for all discovered tandem NLRs in eight gras...
The alignment of NB, ARC1, and ARC2 used to train the HMM for NLR proteins used for phylogenetic ana...
Maximum likelihood phylogeny based on the NB-ARC domain of all NLRs and NLR-IDs for each of the nine...
Manual curation of the genomic regions surrounding MIC1 genes in Brachypodium and rice. (A) MIC1 NLR...
Protein ids and corresponding domains of putative NLR-IDs from all plant species. Table of domain ar...
This Figshare project contains data for paper entitled "Dominant integration locus drives continuous...
Here we identified cell-surface (LRR-RLKs, LRR-RLPs, LysM-RLKs and LysM-RLPs) and intracellular immu...
Data generated associated with understanding the features of NLRs in Arabidopsis Col-0. Contains: ...
Phylogenetic tree of Response Regulators in Arabidopsis thaliana, Cajanus cajan, Cicer arietinum, Gl...
The average neutral divergence rates of different domains in R-genes in the legume family. Note that...