<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Valentina Lorenzi</submitter><organism>Homo sapiens</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-15479</full_dataset_link><description>scATAC-seq of first and second trimester human reproductive tract (including female and male internal and external genitalia)</description><repository>biostudies-arrayexpress</repository><sample_protocol>Library Construction - Library preparation was carried out according to the manufacturer’s protocol.</sample_protocol><sample_protocol>Sequencing - Libraries for scATAC-seq were sequenced on Illumina NovaSeq 6000, aiming at a minimum coverage of 10,000 fragments per cell, with the following sequencing format; read 1: 50 cycles; i7 index: 8 cycles, i5 index: 16 cycles; read 2: 50 cycles.</sample_protocol><sample_protocol>Sample Collection - Single-nuclei suspensions were isolated from dissociated cells when performing scATAC-seq, following the manufacturers’ instructions, and from frozen tissue sections when performing multiomic snRNA-seq/scATAC-seq. For the latter, thick (300 µm) sections were cryosectioned, and kept in a tube on dry ice until subsequent processing. Nuclei were released via Dounce homogenisation as described in detail in the protocols.io.</sample_protocol><sample_protocol>Nucleic Acid Extraction - For the scATAC-seq and multimodal snRNA-seq/scATAC-seq experiments, cells were loaded according to the manufacturer’s protocol for the Chromium Single Cell ATAC v2  and Chromium Next GEM Single Cell Multiome ATAC+Gene Expression (10X Genomics) to attain between 2,000 and 10,000 cells per well.</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>Processed Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><data_protocol>Data Transformation - scATAC-seq libraries were processed (read filtering, alignment, barcode counting, and cell calling) with 10x Genomics Cell Ranger ATAC pipeline v.2 using the pre-built 10x GRCh38 genome (version 3.1.0) as reference.</data_protocol><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><instrument_platform>Illumina NovaSeq 6000</instrument_platform><study_type>scATAC-seq</study_type><species>Homo sapiens</species><pubmed_authors>Roser Vento Tormo</pubmed_authors><pubmed_authors>Valentina Lorenzi</pubmed_authors><pubmed_authors>Luz Garcia Alonso</pubmed_authors></additional><is_claimable>false</is_claimable><name>scATAC-seq of first and second trimester human reproductive tract</name><description>scATAC-seq of first and second trimester human reproductive tract (including female and male internal and external genitalia)</description><dates><release>2025-08-07T00:00:00Z</release><modification>2025-08-07T23:45:50.117Z</modification><creation>2025-08-07T23:45:50.117Z</creation></dates><accession>E-MTAB-15479</accession><cross_references><ENA>ERP178531</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0010891</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>