<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>17(1)</volume><submitter>Zhang W</submitter><pubmed_abstract>Tea plants possess a highly heterozygous genome and produce diverse beneficial metabolites, yet the genomic basis of its metabolic diversity remains fully elusive. Here, we show that single-cell sequencing of 107 sperm cells, combined with PacBio HiFi and ONT ultra-long sequencing, enables an accurate haplotype-resolved genome assembly of Fuding Dabaicha (FDDB). Structural variations (SVs) between the two haplotypes comprise 23.8% of the genome and strongly influence crossover patterns. Using these phased genomes, we establish a half-sib-based QTL mapping platform and identify a Gypsy LTR insertion in the promoter of CsDFRb, which associated with the increasing of p-coumaroylquinate levels in young leaves. Moreover, mGWAS reveals 2649 additional loci associated with 2837 metabolites when u</pubmed_abstract><journal>Nature communications</journal><pagination>1754</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12913673</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The Camellia sinensis var. sinensis cv. Fuding Dabaicha genome unveils structural variation-driven metabolic innovation.</pubmed_title><pmcid>PMC12913673</pmcid><pubmed_authors>Zhang W</pubmed_authors><pubmed_authors>Fernie AR</pubmed_authors><pubmed_authors>Jiang X</pubmed_authors><pubmed_authors>Tariq A</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Buchmann J</pubmed_authors><pubmed_authors>Luo S</pubmed_authors><pubmed_authors>Usadel B</pubmed_authors><pubmed_authors>Wen W</pubmed_authors><pubmed_authors>Gao D</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Camellia sinensis var. sinensis cv. Fuding Dabaicha genome unveils structural variation-driven metabolic innovation.</name><description>Tea plants possess a highly heterozygous genome and produce diverse beneficial metabolites, yet the genomic basis of its metabolic diversity remains fully elusive. Here, we show that single-cell sequencing of 107 sperm cells, combined with PacBio HiFi and ONT ultra-long sequencing, enables an accurate haplotype-resolved genome assembly of Fuding Dabaicha (FDDB). Structural variations (SVs) between the two haplotypes comprise 23.8% of the genome and strongly influence crossover patterns. Using these phased genomes, we establish a half-sib-based QTL mapping platform and identify a Gypsy LTR insertion in the promoter of CsDFRb, which associated with the increasing of p-coumaroylquinate levels in young leaves. Moreover, mGWAS reveals 2649 additional loci associated with 2837 metabolites when u</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-07-16T06:52:09.038Z</modification><creation>2026-07-09T10:42:18.628Z</creation></dates><accession>S-EPMC12913673</accession><cross_references><pubmed>41535305</pubmed><doi>10.1038/s41467-026-68463-8</doi></cross_references></HashMap>