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Sample GSM3507347 Query DataSets for GSM3507347
Status Public on May 02, 2019
Title Mouse1-Channel6
Sample type SRA
 
Source name Whole adult mouse brain
Organism Mus musculus
Characteristics tissue: whole brain
bead concentration: 5000
mouse id: Mouse1
Growth protocol Flash frozen adult mouse whole brain tissue was purchased from BrainBits (SKU: C57AWB)
Extracted molecule genomic DNA
Extraction protocol Nuclei isolation was performed using the Omni-ATAC protocol for isolation of nuclei from frozen tissues. Nuclei were resuspended in Whole Cell Tagmentation Mix containing 0.1% Tween-20, 0.01% Digitonin, 1X PBS supplemented with 0.1% BSA, ATAC Tagmentation Buffer and ATAC Tagmentation Enzyme (parts of the SureCell ATAC-Seq Library Prep Kit - 17004620, Bio-Rad). Cells were mixed and agitated on a ThermoMixer for 30 min at 37°C. Tagmented cells were kept on ice prior to encapsulation.
Tagmented nuclei were loaded onto a ddSEQ Single-Cell Isolator (12004336, Bio-Rad). Single-cell ATAC-Seq libraries were prepared using the SureCell ATAC-Seq Library Prep Kit (17004620, Bio-Rad) and SureCell ddSEQ Index Kit (12009360, Bio-Rad). Bead barcoding and sample indexing was performed in a C1000 Touch™ Thermal cycler with a 96-Deep Well Reaction Module (1851197, Bio-Rad): 37°C for 30 min, 85°C for 10 min, 72°C for 5 min, 98°C for 30 sec, 8 cycles of 98°C for 10 sec, 55°C for 30 sec, and 72°C for 60 sec, and a single 72°C extension for 5 min to finish. Emulsions were broken and products cleaned up using Ampure XP beads (A63880, Beckman Coulter). Barcoded ATAC amplicons were further amplified using a C1000 Touch™ Thermal cycler with a 96-Deep Well Reaction Module: 98°C for 30 sec, 6-9 cycles (cycle number depending on the cell input, Section 4 Table 3 of the User Guide) of 98°C for 10 sec, 55°C for 30 sec, and 72°C for 60 sec, and a single 72°C extension for 5 min to finish. PCR products were purified using Ampure XP beads and quantified on an Agilent Bioanalyzer (G2939BA, Agilent) using the High-Sensitivity DNA kit (5067-4626, Agilent). Libraries were loaded at 1.5 pM on a NextSeq 550 (SY-415-1002, Illumina) using the NextSeq High Output Kit (150 cycles; 20024907, Illumina) and sequencing was performed using the following read protocol: Read 1 118 cycles, i7 index read 8 cycles, and Read 2 40 cycles. A custom sequencing primer is required for Read 1 (16005986, Bio-Rad; included in the kit).
 
Library strategy ATAC-seq
Library source genomic
Library selection other
Instrument model NextSeq 550
 
Data processing Barcode sequences were parsed and trimmed from FASTQs using custom python scripts implemented in the bap-barcode module.
Paired-end reads were aligned to mm10 using bwa.
Duplicate reads and all downstream processing was performed using the bead-based scATAC-seq processing (bap) tool.
Genome_build: mm10
Supplementary_files_format_and_content: Decomposed counts matrix. CountsData is indexed by peak (row), cell (column), and count where the Bed file and CellData provide annotations for rows and columns. Barcode translate file maps raw sequence barcode (many) to cell barcode (one) from the bap output. The BarcodeLogic Excel file contains the information needed to parse the cell barcode from the sequencing data.
Supplementary_files_format_and_content: mousebrain_BarcodeLogic.xlsx: BeadStructure
 
Submission date Dec 10, 2018
Last update date Jun 26, 2019
Contact name Caleb Lareau
E-mail(s) lareauc@mskcc.org
Organization name Memorial Sloan Kettering
Street address 417 E 68th St, Zuckerman - ZRC 1132
City New York
State/province New York
ZIP/Postal code 10065
Country USA
 
Platform ID GPL21626
Series (2)
GSE123576 High-throughput combinatorial indexing enables scalable single-cell chromatin accessibility profiling [mouse brain]
GSE123581 Droplet-based combinatorial indexing for massive-scale single-cell chromatin accessibility
Relations
BioSample SAMN10574896
SRA SRX5124225

Supplementary file Size Download File type/resource
GSM3507347_Mouse1-Channel6.fragments.tsv.gz 1.3 Gb (ftp)(http) TSV
GSM3507347_Mouse1-Channel6.fragments.tsv.gz.tbi 630.8 Kb (ftp)(http) TBI
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Raw data are available in SRA
Processed data are available on Series record

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