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Because durum and bread wheat share the same ancestral A and B subgenomes, the added resistance in bread wheat may stem from D subgenome contributions.
Establishing the gene-space as a reference is even more challenging as the three homeologous genomes of polyploid bread wheat share a high level of sequence similarity.
Therefore, the three homoeologues of the same locus in bread wheat share high sequence similarity that could illustrate the flexibility of a polyploidy species in which due to the mutation in one homoeologue may be compensated for by the homoeologue [ 29].
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T. urartu and common wheat shared two genes, A3-391 and A3-400.
Wheat shared a common ancestor with rice approximately 40 54 million years BC, and the divergence time of Brachypodium from other gramineous plants was approximately 32 39 million years BC.
All the above evidences collectively suggest that wheat shared a "cross-tolerance" in the molecular functions responsive to heat, drought and their combination, and possibly biotic stress.
Because Aegilops and wheat species share a recent common evolutionary history, involving frequent polyploidy events, it is inherently difficult to distinguish introgression from incomplete lineage sorting.
A number of cultivars from the CA spring wheat population share ancestry with the lines from the CIMMYT population and nearly all SD and MN spring cultivars were assigned to the same cluster.
All wheat ESTs sharing high similarity with the reference gene were subjected to contig assembly.
Genomic analysis revealed that the wheat genome shared some microbial genetic fragments, which were specifically induced in response to Bgt and Pst infection.
Our experiment showed that the wheat line shared some microbial genetic materials with the pathogens, which may be exploited to resist infection by a virulent fungal pathogen.
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