|
Status |
Public on Apr 20, 2024 |
Title |
MAP8.B6.Ly49h_WT_Hn_RNA |
Sample type |
SRA |
|
|
Source name |
Spleen
|
Organism |
Mus musculus |
Characteristics |
strain: C57BL/6J tissue: Spleen cell type: Natural killer cells subset: Ly49H- genotype: MAP8.B6.Ly49h_WT/Ly49KO treatment: ex vivo marker: singlet CD4-CD8-TCRBeta-CD19-NK1.1+NKp46+CD49a-CD49b+
|
Treatment protocol |
Splenic NK cells were FACS-sorted from mice
|
Extracted molecule |
polyA RNA |
Extraction protocol |
Total RNA from sorted cells was extracted using Quick-RNA Microprep Kit (Zymo Research, R1050). 50-100 ng of total RNA was processed with NEBNext Poly(A) mRNA Magnetic Isolation Module (NEB, E7490) and NEBNext Ultra II Directional RNA Library Prep Kit (NEB, E7760) to generate mRNA-seq libraries
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|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NextSeq 500 |
|
|
Description |
singlet CD4-CD8-TCRβ-CD19-NK1.1+NKp46+CD49a-CD49b+
|
Data processing |
STAR (v 2.5.4b) was used for alignment “sambamba markdup” was used to remove PCR duplicates from paired-end libraries reads with MAPQ < 30 were removed "featureCounts -t exon --fracOverlap 0.5” from subread (v2.0.0) was used to count the number of reads overlapping the exons of each gene Assembly: mm10 Supplementary files format and content: tsv: raw read counts for each gene in each sample
|
|
|
Submission date |
Mar 02, 2023 |
Last update date |
Apr 20, 2024 |
Contact name |
Changxu Fan |
E-mail(s) |
fanc@wustl.edu
|
Organization name |
Washington University in St. Louis
|
Department |
Genetics
|
Lab |
Ting Wang Lab
|
Street address |
4515 McKinley Avenue, Room 5213
|
City |
Saint Louis |
State/province |
Missouri |
ZIP/Postal code |
63110 |
Country |
USA |
|
|
Platform ID |
GPL19057 |
Series (2) |
GSE226497 |
Epigenetic evolution of the Ly49 gene family [RNA-seq] |
GSE226502 |
Epigenetic evolution of the Ly49 gene family |
|
Relations |
BioSample |
SAMN33571788 |
SRA |
SRX19551509 |