The study screened 6,274 elite rice genotypes for submergence and stagnant flooding tolerance, identifying 89 lines with superior performance, including 37 that outperformed SUB1A introgression lines by 40‑50%. These elite lines harbor 86 key QTLs/genes and were used in a novel Transition from Trait to Environment (TTE) breeding strategy, achieving a 65% genetic gain for submergence tolerance and demonstrating strong performance in flood‑prone regions of India and Bangladesh.

The study performed transcriptome profiling of Cryptomeria japonica individuals from different geographic origins grown in three common gardens across Japan, assembling 77,212 transcripts guided by the species' genome. Using SNP-based genetic clustering and weighted gene co‑expression network analysis, they identified gene modules whose expression correlated with genetic differentiation, revealing that defense‑related genes are up‑regulated in Pacific‑side populations while terpenoid metabolism genes are higher in Sea‑of‑Japan populations, indicating local adaptation via regulatory changes.

A biparental Vicia faba mapping population was screened under glasshouse conditions for resistance to a mixture of Fusarium avenaceum and Fusarium oxysporum, revealing several families with moderate to high resistance. Using the Vfaba_v2 Axiom SNP array, a high-density linkage map of 6,755 SNPs was constructed, enabling the identification of a major QTL on linkage group 4 associated with partial resistance to foot and root rot.

The study investigates how miR394 influences flowering time in Arabidopsis thaliana by combining transcriptomic profiling of mir394a mir394b double mutants with histological analysis of reporter lines. Bioinformatic analysis identified a novel lncRNA overlapping MIR394B (named MIRAST), and differential promoter activity of MIR394A and MIR394B suggests miR394 fine‑tunes flower development through transcription factor and chromatin remodeler regulation.

The study investigated unexpected leaf spot symptoms in Psa3‑resistant kiwifruit (Actinidia) germplasm, finding that Psa3 was detectable by qPCR and metabarcoding despite poor culturing. Metabarcoding revealed distinct bacterial community shifts in lesions versus healthy tissue, and whole‑genome sequencing identified diverse Pseudomonas spp. that, while not individually more pathogenic, could enhance Psa3 growth, suggesting pathogenic consortia on resistant hosts.

The study characterized 1,264 maize near‑isogenic lines derived from 18 donor inbreds crossed to the recurrent parent B73, using genotyping‑by‑sequencing and SNP‑chip data to detect 2,972 introgression segments via a novel hidden Markov model pipeline. Disease phenotyping enabled QTL mapping for foliar disease resistance, revealing extensive allelic variation among donor lines, and establishing the nNIL population as a valuable resource for dissecting complex traits in maize.