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Status |
Public on Jul 01, 2015 |
Title |
lympho-pelleted |
Sample type |
SRA |
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Source name |
Lymphocytes
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Organism |
Homo sapiens |
Characteristics |
sample type: With ribosome purification cell type: Lymphocytes
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Treatment protocol |
-
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Growth protocol |
RPMI + 15% FBS, 37C, 5% CO2
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Extracted molecule |
total RNA |
Extraction protocol |
Cells lysed in 200 mM KOAC, 15 mM MgCl, 15 mM K-HEPES pH 7.2, 180 uM cycloheximide. Treated with 10 ug/ml Mnase for 30 min NEB Directional Small RNA kit. Libraries purified by gel electrophoresis
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Library strategy |
OTHER |
Library source |
transcriptomic |
Library selection |
other |
Instrument model |
Illumina HiSeq 2500 |
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Data processing |
Cutadapt Trim AAGATCGGAAGAGCACACGTCT cutadapt -a AAGATCGGAAGAGCACACGTCT --discard-untrimmed -m 20 DBA37-P.fastq -o trimDBA37-P.fastq cutadapt 1.6 with Python 2.7.6 Bowtie bowtie -p 7 -v 0 --norc database/chosenTranscripts reads/trimDBA37-P.fastq mapped/DBA37-P.map Bowtie 1.1.1 Genome_build: NCBI v37 Supplementary_files_format_and_content: XLSX; RPKM values for all genes within the coding sequence
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Submission date |
Apr 17, 2015 |
Last update date |
May 15, 2019 |
Contact name |
David Reid |
Organization name |
Duke University
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Department |
Biochemistry
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Lab |
Nicchitta
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Street address |
436 Nanaline Duke Bldg., Box 3709 DUMC
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City |
Durham |
State/province |
NC |
ZIP/Postal code |
27710 |
Country |
USA |
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Platform ID |
GPL16791 |
Series (1) |
GSE68008 |
Methods comparison for ribosome profiling |
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Relations |
BioSample |
SAMN03490543 |
SRA |
SRX998838 |
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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