Manual curation of the genomic regions surrounding MIC1 genes in Brachypodium and rice. (A) MIC1 NLR-IDs and surrounding genes. (B) Additional microsynteny analyses between rice and B. distachyon. (PPTX 150 kb
Figure S4. MapMan analysis of the genes and pathways responsive to the pathogenic invasion using the...
Ratio distribution of Nipponbare or Minghui63 highly expressed genes to every 100 mapped genes. (PDF...
GO enrichment analysis of tissue specific changed-tissues jiDE genes of the NM combination. (XLSX 49...
Locations, gene identifiers, and tandem classifications for all discovered tandem NLRs in eight gras...
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 alignment of NB, ARC1, and ARC2 used to train the HMM for NLR proteins used for phylogenetic ana...
Quality assessment of the gene datasets used for phylogenetic analysis: N50 and size of the correspo...
Clade memberships of all NLRs present in the tree in Fig. 1 and corresponding integrated domains pr...
The AP2b/MYB-NLR domain shuffling includes duplication of AP2 gene and inter-chromosomal transfer of...
Potential donor - NLR acceptor gene sets, as observed from phylogenetic trees of the donor ID genes....
Maximum likelihood phylogeny based on the NB-ARC domain of all NLRs and NLR-IDs for each of the nine...
This Figshare project contains data for paper entitled "Dominant integration locus drives continuous...
GO enrichment analysis of global jiDE genes of the NM combination. (XLSX 57Â kb) (XLSX 52Â kb
Highly expressed genes and the two types of jiDE genes of the two japonica-indica combinations in th...
Figure S4. MapMan analysis of the genes and pathways responsive to the pathogenic invasion using the...
Ratio distribution of Nipponbare or Minghui63 highly expressed genes to every 100 mapped genes. (PDF...
GO enrichment analysis of tissue specific changed-tissues jiDE genes of the NM combination. (XLSX 49...
Locations, gene identifiers, and tandem classifications for all discovered tandem NLRs in eight gras...
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 alignment of NB, ARC1, and ARC2 used to train the HMM for NLR proteins used for phylogenetic ana...
Quality assessment of the gene datasets used for phylogenetic analysis: N50 and size of the correspo...
Clade memberships of all NLRs present in the tree in Fig. 1 and corresponding integrated domains pr...
The AP2b/MYB-NLR domain shuffling includes duplication of AP2 gene and inter-chromosomal transfer of...
Potential donor - NLR acceptor gene sets, as observed from phylogenetic trees of the donor ID genes....
Maximum likelihood phylogeny based on the NB-ARC domain of all NLRs and NLR-IDs for each of the nine...
This Figshare project contains data for paper entitled "Dominant integration locus drives continuous...
GO enrichment analysis of global jiDE genes of the NM combination. (XLSX 57Â kb) (XLSX 52Â kb
Highly expressed genes and the two types of jiDE genes of the two japonica-indica combinations in th...
Figure S4. MapMan analysis of the genes and pathways responsive to the pathogenic invasion using the...
Ratio distribution of Nipponbare or Minghui63 highly expressed genes to every 100 mapped genes. (PDF...
GO enrichment analysis of tissue specific changed-tissues jiDE genes of the NM combination. (XLSX 49...