|
Status |
Public on May 29, 2019 |
Title |
brain.Se0.1.rep3 |
Sample type |
SRA |
|
|
Source name |
Mouse fed with 0.1 ppm dietary Se for 5 weeks
|
Organism |
Mus musculus |
Characteristics |
strain: C57Bl/6J gender: male pathology: No gross pathology observed tissue: Mouse whole brain
|
Treatment protocol |
Eight-weeks old C57BL/6J male mice were fed with diet supplemented with either 0, 0.1, 0.4 or 2.25 ppm for five weeks
|
Growth protocol |
Normal chow until the Se diet was fed
|
Extracted molecule |
total RNA |
Extraction protocol |
TRIzolĀ® Reagent (Thermo Fisher Scientific) TruSeq Stranded Total RNA Kit (Illumina; RS-122-2201)
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2500 |
|
|
Data processing |
Samples were pooled and sequenced on one HiSeq run using Illumina TruSeq Stranded Total RNA Kit RS-122-2201. Basecalling was performed by RTA (version 1.18.64). Demultiplexing and FASTQ generation was performed using bcl2fastq (version 2.17) allowing 1 mismatch. Reads were filtered with a base call quality >94% of bases with Q30 and and above. Trimming of adapters and low-quality bases was performed using Trimmomatic (version 0.33). First pass alignment of reads to the mm10 reference genome was performed using STAR (version 2.5.2b) with parameters: STAR --genomeDir /path/to/genomeDir --outFilterIntronMotifs RemoveNoncanonicalUnannotated --outSAMstrandField None --outFilterType BySJout --outFilterMultimapNmax 20 --alignSJoverhangMin 8 --alignSJDBoverhangMin 1 --outFilterMismatchNmax 999 --outFilterMismatchNoverLmax 0.3 --alignIntronMin 20 --alignIntronMax 1000000 --alignMatesGapMax 1000000 --clip3pAdapterSeq - --readFilesIn /path/to/read1.fastq.gz /path/to/read2.fastq.gz --readFilesCommand zcat --runThreadN 32 --outFileNamePrefix <prefix> --outSAMtype BAM Unsorted Second pass alignment of reads to the mm10 reference genome was performed using STAR (version 2.5.2b) with parameters: STAR --genomeDir /path/to/genomeDir --outFilterIntronMotifs RemoveNoncanonicalUnannotated --outSAMstrandField None --outFilterType BySJout --outFilterMultimapNmax 20 --alignSJoverhangMin 8 --alignSJDBoverhangMin 1 --outFilterMismatchNmax 999 --outFilterMismatchNoverLmax 0.3 --alignIntronMin 20 --alignIntronMax 1000000 --alignMatesGapMax 1000000 --clip3pAdapterSeq - --readFilesIn /path/to/read1.fastq.gz /path/to/read2.fastq.gz --readFilesCommand zcat --runThreadN 32 --outFileNamePrefix <prefix> --outSAMunmapped Within --outWigType None --outWigStrand Stranded --sjdbFileChrStartEnd /path/to/sjdbFile.txt --sjdbGTFfile /path/to/annotations.gtf --limitSjdbInsertNsj 4000000 --quantMode TranscriptomeSAM GeneCounts --outSAMtype BAM SortedByCoordinate Gene-level expression quantificiation and library size normalization in counts-per-million was performed using RSEM (version 1.3.0). Quantile-normalization and differential expression was performed using limma-voom (version 3.34.5). Genome_build: mm10 Supplementary_files_format_and_content: Tab-delimited text files are limma-voom normalized differential expression output.
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|
|
Submission date |
Apr 01, 2019 |
Last update date |
May 29, 2019 |
Contact name |
Sun Hee Yim |
E-mail(s) |
shyim@rics.bwh.harvard.edu
|
Phone |
6176510330
|
Organization name |
BWH/Harvard Medical School
|
Department |
Medicine
|
Lab |
Genetics
|
Street address |
77 Ave Louis Pasteur, RM435
|
City |
Boston |
State/province |
MA |
ZIP/Postal code |
02115 |
Country |
USA |
|
|
Platform ID |
GPL17021 |
Series (1) |
GSE129138 |
Selenium Deficiency is Associated with Pro-Longevity Mechanisms |
|
Relations |
BioSample |
SAMN11309377 |
SRA |
SRX5620707 |