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Status |
Public on Jan 11, 2024 |
Title |
Organoids EM, DM, and ALI day 0, day 3 and ALI + IL4/13 |
Sample type |
SRA |
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Source name |
Human conjunctiva organoids - CMO303/TX294: donor 16, p5; CMO304/TX295: donor 16, p4; CMO305/TX296: donor 16, p6; CMO306/TX297: donor 16, p5; CMO307/TX298: donor 4, p4
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Organism |
Homo sapiens |
Characteristics |
cell line: Human conjunctiva organoids - CMO303/TX294: donor 16, p5; CMO304/TX295: donor 16, p4; CMO305/TX296: donor 16, p6; CMO306/TX297: donor 16, p5; CMO307/TX298: donor 4, p4 treatment: EM (donor 16, p5, CMO303/TX294), DM (donor 16, p4, CMO304/TX295), ALI day 0 (donor 16, p6, CMO305/TX296), ALI day 3 (donor 16, p5, CMO306/TX297), ALI day 17 + IL4/13 (donor 4, p4, CMO307/TX298)
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Extracted molecule |
polyA RNA |
Extraction protocol |
Tissue samples were obtained one month before the processing. At time of sampling, these were immediately minced in the operating room and placed in 1 mL of CellBanker 1 (Amsbio, 11888) on dry ice. The samples were stored at -80 °C until further processing. On the day of the sort, the 4 biopsies were thawed, pooled and washed with 10 mL of AdDMEM+++. To dissociate the samples, cells were resuspended in 1 mL of 0.25% Trypsin/EDTA (Gibco) and 10 U/mL DNase I (Sigma Aldrich, DN25) and incubated in a 37 °C water bath, while checking the advancement of dissociation regularly under the microscope. Using a pre-wet narrowed Pasteur pipette, the cell suspensions were mechanically dissociated by pipetting up and down. The cell suspensions were washed twice with AdDMEM+++. The cell suspensions from 17 day-old ALI cultures were resuspended in 1 mL FACS buffer (PBS-MQ + 10% Fetal bovine serum - Sigma-Aldrich, F7524). The tissue cell suspension was treated for 5 minutes at RT with red blood cell lysis buffer (Sigma Aldrich, 11814389001), before being washed once with AdDMEM+++. Finally, the cell suspension was resuspended in 1 mL FACS buffer. The cell suspensions that were multiplexed (i.e. conditions 1, 2, 3, 4 and 6) were incubated in labelling oligos CMO303, CMO304, CMO305, CMO306 and CMO307, respectively, for 15 minutes at RT. Then, cells were washed with 6 mL FACS buffer and resuspended in 1 mL of FACS buffer. Immediately before the sort, DAPI (ThermoFisher Scientific, D1306) and DRAQ5 (Biostatus, 62251) were added to the cell suspensions. Living cells (that is DAPI- and DRAQ5+) were sorted on a BD Jazz sorter (BD Bioscience) into FACS buffer. 30,000 cells were used for library preparation. Libraries were prepared using the 10x Genomics Chromium 3’ Gene Expression solution v3.1
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Library strategy |
RNA-Seq |
Library source |
transcriptomic single cell |
Library selection |
cDNA |
Instrument model |
Illumina NovaSeq 6000 |
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Description |
10x Genomics LX255_LX256
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Data processing |
Illumina output (bcl files) converted to fastq files using mkfastq (CellRanger v7.0.1) Alignment, filtering, barcode and UMI counting done using cellranger count (CellRanger v7.0.1) For tissue samples, SNP-based demultiplexing using souporcell Assembly: Genome Reference Consortium Human Build 38 Supplementary files format and content: Per sample filtered_feature_bc_matrix output from CellRanger (v7.0.1); includes gene-barcode matrices, genes, barcodes (demultiplexed for LX255_LX256) Supplementary files format and content: For tissue sample, Souporcell output for k= 4 clusters
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Submission date |
Sep 05, 2023 |
Last update date |
Jan 11, 2024 |
Contact name |
Marie Bannier-Hélaouët |
E-mail(s) |
m.bannier@hubrecht.eu
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Organization name |
Hubrecht Institute
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Street address |
Uppsalalaan 8
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City |
Utrecht |
ZIP/Postal code |
3584CT |
Country |
Netherlands |
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Platform ID |
GPL24676 |
Series (1) |
GSE242382 |
Single-cell characterization of human conjunctiva tissue, organoids and air-liquid interface cultures (10X) |
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Relations |
BioSample |
SAMN37285146 |
SRA |
SRX21637689 |
Supplementary file |
Size |
Download |
File type/resource |
GSM7761925_TX294_barcodes.tsv.gz |
9.5 Kb |
(ftp)(http) |
TSV |
GSM7761925_TX294_features.tsv.gz |
325.8 Kb |
(ftp)(http) |
TSV |
GSM7761925_TX294_matrix.mtx.gz |
19.6 Mb |
(ftp)(http) |
MTX |
GSM7761925_TX295_barcodes.tsv.gz |
18.6 Kb |
(ftp)(http) |
TSV |
GSM7761925_TX295_features.tsv.gz |
325.8 Kb |
(ftp)(http) |
TSV |
GSM7761925_TX295_matrix.mtx.gz |
36.5 Mb |
(ftp)(http) |
MTX |
GSM7761925_TX296_barcodes.tsv.gz |
9.9 Kb |
(ftp)(http) |
TSV |
GSM7761925_TX296_features.tsv.gz |
325.8 Kb |
(ftp)(http) |
TSV |
GSM7761925_TX296_matrix.mtx.gz |
18.3 Mb |
(ftp)(http) |
MTX |
GSM7761925_TX297_barcodes.tsv.gz |
10.2 Kb |
(ftp)(http) |
TSV |
GSM7761925_TX297_features.tsv.gz |
325.8 Kb |
(ftp)(http) |
TSV |
GSM7761925_TX297_matrix.mtx.gz |
15.4 Mb |
(ftp)(http) |
MTX |
GSM7761925_TX298_barcodes.tsv.gz |
51.9 Kb |
(ftp)(http) |
TSV |
GSM7761925_TX298_features.tsv.gz |
325.8 Kb |
(ftp)(http) |
TSV |
GSM7761925_TX298_matrix.mtx.gz |
109.4 Mb |
(ftp)(http) |
MTX |
SRA Run Selector |
Raw data are available in SRA |
Processed data provided as supplementary file |
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