<HashMap><database>biostudies-arrayexpress</database><scores/><additional><omics_type>Metabolomics</omics_type><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><submitter>Magdalena Kroc</submitter><instrument_platform>Illumina NovaSeq X</instrument_platform><study_type>ChIP-seq</study_type><organism>Lupinus angustifolius</organism><species>Lupinus angustifolius</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-16430</full_dataset_link><description>In this study we used DNA affinity purification sequencing (DAP-seq) to identify genome-wide binding of allele-specific RAP2-7 transcription factor variants in five narrow-leafed lupin (Lupinus angustifolius L.) genotypes with contrasting alkaloid regulation, including low-alkaloid iucundus line (83A:476), high-alkaloid Iucundus line (P27255) and three Bryansk low-alkaloid lines (95826 (Bryanskij-35), 95927 (Bryanskij-123) and 95928 (Bryanskij-237/83)).</description><repository>biostudies-arrayexpress</repository><sample_protocol>Growth Protocol - Plants were cultivated in a growth chamber (16 h photoperiod, 22/18 °C day/night, 55–60% relative humidity, until they reached whole plant flowering stage.</sample_protocol><sample_protocol>Sample Collection - The immobilized Halo-tagged allele-specific RAP2-7 protein was incubated with the adapter-ligated DNA library. After incubation, the beads were washed, and the bound DNA was recovered, PCR-amplified, purified, and quantified. Negative controls were processed in parallel using adapter-ligated DNA libraries incubated with Magne HaloTag beads in the absence of recombinant protein. For more details please see accompanying manuscript.</sample_protocol><sample_protocol>Nucleic Acid Extraction - High-molecular-weight genomic DNA for DAP-seq was extracted from frozen young leaves (3 g) using a phenol:chloroform:isoamyl alcohol protocol, and quantified fluorometrically using the Qubit dsDNA Broad Range Assay (Thermo Fisher Scientific).</sample_protocol><sample_protocol>Library Construction - Genomic DNA libraries were prepared according to Bartlett et al. (2017; doi.org/10.1038/nprot.2017.055), with minor modifications. For more details please see accompanying manuscript.</sample_protocol><sample_protocol>Sequencing - Samples were sequenced on an Illumina NovaSeq X Plus (PE150), at Novogene (HK) Co. Ltd., generating ~6 Gb of raw data per sample (≥20 million reads per sample).</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><pubmed_authors>Katarzyna Czepiel</pubmed_authors><pubmed_authors>Magdalena Kroc</pubmed_authors><pubmed_authors>Grzegorz Koczyk</pubmed_authors></additional><is_claimable>false</is_claimable><name>RAP2-7 DAP-seq (Lupinus angustifolius L.)</name><description>In this study we used DNA affinity purification sequencing (DAP-seq) to identify genome-wide binding of allele-specific RAP2-7 transcription factor variants in five narrow-leafed lupin (Lupinus angustifolius L.) genotypes with contrasting alkaloid regulation, including low-alkaloid iucundus line (83A:476), high-alkaloid Iucundus line (P27255) and three Bryansk low-alkaloid lines (95826 (Bryanskij-35), 95927 (Bryanskij-123) and 95928 (Bryanskij-237/83)).</description><dates><release>2026-06-30T00:00:00Z</release><modification>2026-06-30T01:00:54.36Z</modification><creation>2025-12-19T12:58:40.611Z</creation></dates><accession>E-MTAB-16430</accession><cross_references><ENA>ERP186833</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0002692</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>