|
Status |
Public on Mar 14, 2024 |
Title |
Young_Endo_Tterm_replicate2_ATACseq |
Sample type |
SRA |
|
|
Source name |
B16-OVA Tumor
|
Organism |
Mus musculus |
Characteristics |
cell type: CD8+ T cells cell subset: Tterm cell state: terminally exhausted tissue: B16-OVA Tumor strain: C57BL/6J age: 10-12 weeks old sequencing batch: Batch 1 & 2 genotype: Wild type
|
Extracted molecule |
genomic DNA |
Extraction protocol |
DNA was purified using a QIAgen MinElute Reaction Cleanup kit Post-PCR bead cleanup was done using Agencourt AMPure XP bead cleanup (Beckman Coulter/Agencourt), and library quality was verified using Tapestation analysis.
|
|
|
Library strategy |
ATAC-seq |
Library source |
genomic |
Library selection |
other |
Instrument model |
NextSeq 1000 |
|
|
Description |
Young_Endo_Tterm_2 NormCountsATAC_Endo.txt
|
Data processing |
Raw fastq files were downloaded from Illumina BaseSpace and merged across lanes Quality trimming and primer removal in raw fastq files were done with Trimmomatric (v.0.36) using the following parameters: LEADING:15 TRAILING:15 SLIDINGWINDOW:4:15 MINLEN:30 CROP:35. Trimmed reads were aligned to mm10 with Bowtie2 (v.2.2.9) using a maximum insert size of 1,000. Aligned bams were sorted, duplicates marked (Picard v.2.8.0) , and reads mapping to the blacklist region removed. Peak-calling using MACS (v.2.1.1) was performed on merged bam files (Samtools v. 1.3.1) from biological replicates using a q-value threshold of 0.001. Consensus peaks from all biological conditions were merged to create a single peak universe. Cut sites were extracted from each biological replicate and the number of cuts in each peak region was quantified to generate a raw counts matrix. Normalization and differential expression were performed using DESeq2 (v 1.28.1) Assembly: mm10 Supplementary files format and content: tab-delimited text file including DESeq2 normalized counts
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|
|
Submission date |
Feb 06, 2024 |
Last update date |
Mar 14, 2024 |
Contact name |
Alex Chang-Yu Chen |
E-mail(s) |
cachen@mgh.harvard.edu
|
Organization name |
Massachusetts General Hospital
|
Department |
Krantz Family Center for Cancer Research
|
Lab |
Sen Lab
|
Street address |
149 13th Street, 7th floor, Room 7103
|
City |
Boston |
State/province |
MA |
ZIP/Postal code |
02129 |
Country |
USA |
|
|
Platform ID |
GPL32159 |
Series (1) |
GSE255230 |
Changes in chromatin accessibility in intratumoral CD8+ T cell subsets between young and aged TME |
|
Relations |
BioSample |
SAMN39849084 |
SRA |
SRX23556328 |