<HashMap><database>biostudies-arrayexpress</database><scores/><additional><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><submitter>Helen Parker</submitter><instrument_platform>Illumina NovaSeq X</instrument_platform><study_type>DNA-seq</study_type><organism>Homo sapiens</organism><species>Homo sapiens</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-16840</full_dataset_link><description>Targeted non-coding and coding sequencing of patients with SMZL to identify disease relevant mutations</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sequencing - Illumina Novaseq</sample_protocol><sample_protocol>Library Construction - Agilent SureSelect XT HS2 Targeted Enrichment</sample_protocol><sample_protocol>Sample Collection - peripheral blood mononuclear cell sample taken by venipuncture</sample_protocol><sample_protocol>Nucleic Acid Extraction - Qiagen DNeasy blood and tissue column extraction (tumour DNA) and Oragene DNA Saliva kit (saliva DNA)</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>Helen Parker</pubmed_authors></additional><is_claimable>false</is_claimable><name>targeted non-coding and coding sequencing of SMZL patients</name><description>Targeted non-coding and coding sequencing of patients with SMZL to identify disease relevant mutations</description><dates><release>2026-06-04T00:00:00Z</release><modification>2026-06-04T01:03:00.933Z</modification><creation>2026-04-01T10:57:31.95Z</creation></dates><accession>E-MTAB-16840</accession><cross_references><ENA>ERP191661</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0002693</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>