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Status |
Public on Oct 21, 2020 |
Title |
GTT15_P |
Sample type |
SRA |
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Source name |
placenta
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Organism |
Mus musculus |
Characteristics |
tissue: placenta cell type: regulatory T-cell gender: female genotype: Tnfrsf11a (Rank) Foxn1 wild-type pregnancy status: pregnant
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Extracted molecule |
polyA RNA |
Extraction protocol |
Equal numbers of Tregs (280 cells) were sorted from the thymus and placenta of E17.5 pregnant Bl6 females, mated with syngeneic Bl6 males. To increase robustness, the 280 placental Tregs were purified from 5 individual placentas per pregnant female (56 Tregs/placenta). Cells were sorted directly into a cell lysis buffer consisting of a 0.2% (vol/vol) Triton X-100 solution and an RNase inhibitor. For the generation of full-length cDNA, the Smart-seq2 protocol (Picelli, S. et al, Nat Protoc. 2014 Jan;9(1):171-81. doi:10.1038/nprot.2014.006) was used. The subsequent library preparation from the amplified cDNA was performed using the Nextera XT DNA library prep kit (Illumina). For sequencing, libraries were pooled, diluted and sequenced on Illumina HiSeq 3000 using 50 bp single-read chemistry.
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 3000 |
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Description |
Placental Tregs; mice ID GTT15: Pregnant RANK FOXN1 WT
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Data processing |
Illumina HiSeq Control Software (HCS) HD 3.4.0.38 and 3.3.52 was used for the data acquisition on the sequencing instrument. On-instrument base-calling performed by the Illumina Real-Time Analysis (RTA) software 2.7.3 and 2.7.7. BCL to BAM file conversion and demultiplexing with Illumina2bam 1.17 (http://wtsi-npg.github.io/illumina2bam/) and custom programmes based on Picard tools 2.19.2 (https://broadinstitute.github.io/picard/) Spliced genome alignments to GRCm38 (UCSC Genome Browser mm10) and Ensembl reference transcriptome e100 (April 2020) with STAR 2.7.1a and options recommended by the ENCODE project (--alignIntronMax 1000000 --alignIntronMin 20 --alignMatesGapMax 1000000 --alignSJDBoverhangMin 1 --alignSJoverhangMin 8 --outFilterMismatchNmax 999 --outFilterMismatchNoverReadLmax 0.04 --outFilterMultimapNmax 20 --outFilterType BySJout) Differential expression modelling with Bioconductor 3.11 package DESeq2 1.28.1, running under R 4.0.2. Genome_build: UCSC mm10 based on GRCm38 Supplementary_files_format_and_content: Per gene and sample raw (integer) counts and DESeq2-calculated FPKMs in tab-separated value (TSV) format
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Submission date |
Apr 11, 2017 |
Last update date |
Oct 22, 2020 |
Contact name |
Christoph Bock |
E-mail(s) |
cbock@cemm.oeaw.ac.at
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Organization name |
CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences
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Street address |
Lazarettgasse 14
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City |
Vienna |
ZIP/Postal code |
1090 |
Country |
Austria |
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Platform ID |
GPL21493 |
Series (1) |
GSE97666 |
RNA-seq analysis of regulatory T cells in thymus, placenta, spleen and white adipose tissue of pregnant mice |
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Relations |
BioSample |
SAMN06710972 |
SRA |
SRX2733597 |
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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