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Status |
Public on Sep 21, 2018 |
Title |
TAM_B |
Sample type |
SRA |
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Source name |
CT26-Sg-Con implanted tumor
|
Organism |
Mus musculus |
Characteristics |
strain/background: BALB/C genotype/variation: wild type cell type: Tumor-associated macrophages
|
Extracted molecule |
total RNA |
Extraction protocol |
TAMs were isolated from tumors by flow cytometry, flash frozen on dry ice, and RNA was harvested using Trizol reagent. Illumina TruSeq RNA Sample Prep Kit (Cat#FC-122-1001) was used with 1 ug of total RNA for the construction of sequencing libraries. Libraries were prepared using an MGIEasyâ„¢ mRNA kit.
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
BGISEQ-500 |
|
|
Description |
processed data file: TAM.gene.fpkm.txt
|
Data processing |
Illumina Casava1.7 software used for basecalling. Sequenced reads were trimmed for adaptor sequence, and masked for low-complexity or low-quality sequence, then mapped to mm8 whole genome using bowtie v0.12.2 with parameters -q -p 4 -e 100 -y -a -m 10 --best --strata Fragments Per Kilobase Million (FPKM) were calculated using a protocol from Chepelev et al., Nucleic Acids Research, 2009. In short, exons from all isoforms of a gene were merged to create one meta-transcript. The number of reads falling in the exons of this meta-transcript were counted and normalized by the size of the meta-transcript and by the size of the library. Genome_build: mm8 (MGSCv36) Supplementary_files_format_and_content: TAM.gene.fpkm.txt: Tab-delimited text file includes FPKM values for each Sample.
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|
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Submission date |
Sep 20, 2018 |
Last update date |
Sep 21, 2018 |
Contact name |
Haoran Zha |
E-mail(s) |
zhahaoran@tmmu.edu.cn
|
Organization name |
Institute of Cancer, Xinqiao Hospital,Third Military Medical University
|
Street address |
Shaping Street #31
|
City |
Chongqing |
ZIP/Postal code |
400037 |
Country |
China |
|
|
Platform ID |
GPL23479 |
Series (1) |
GSE120274 |
Intracellular activation of complement C3 leads to PD-L1 antibody treatment resistance via modulating tumor-associated macrophages |
|
Relations |
BioSample |
SAMN10075464 |
SRA |
SRX4704234 |