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Status |
Public on Sep 07, 2016 |
Title |
HYGHVBGXX_A8_S296 |
Sample type |
SRA |
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Source name |
Mus musculus CD8 TILs
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Organism |
Mus musculus |
Characteristics |
cell type: CD8 TILs
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Extracted molecule |
total RNA |
Extraction protocol |
TILs were isolated by dissociating tumor tissue in the presence of collagenase D (2.5 mg/ml) for 20 min prior to centrifugation on a discontinuous Percoll gradient (GE Healthcare). Smart-seq2 (Picelli et al., Nature Methods, 2014)
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NextSeq 500 |
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Description |
single-cell RNA-Seq data
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Data processing |
Reads were aligned to a reference genome (mm10 Ensembl) using Bowtie Expression levels were quantified using RSEM (inferred counts and tpm values), and log2(TPM+1) values generated. cells were selected for subsequent analysis based on genecount and mapping rates to transcriptome (see manuscript) Genome_build: mm10 Supplementary_files_format_and_content: text file with tab delimiters
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Submission date |
Aug 24, 2016 |
Last update date |
May 15, 2019 |
Contact name |
Meromit Singer |
E-mail(s) |
msinger@broadinstitute.org
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Organization name |
Broad Institute of MIT and Harvard
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Street address |
415 main st, ROOM 6031
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City |
CAMBRIDGE |
State/province |
MASSACHUSETTS |
ZIP/Postal code |
02142 |
Country |
USA |
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Platform ID |
GPL19057 |
Series (2) |
GSE86030 |
A distinct gene module uncouples dysfunction from activation in tumor-infiltrating T cells (batch 3) |
GSE86042 |
A distinct gene module uncouples dysfunction from activation in tumor-infiltrating T cells |
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Relations |
BioSample |
SAMN05629905 |
SRA |
SRX2051424 |
Supplementary data files not provided |
SRA Run Selector |
Raw data are available in SRA |
Processed data are available on Series record |
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