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Sample GSM2793897 Query DataSets for GSM2793897
Status Public on Mar 28, 2018
Title p_150909_CXT1
Sample type SRA
 
Source name cortex from PND13 mice
Organism Mus musculus
Characteristics tissue: cortex
Treatment protocol tissue grinded in liquid nitrogen and crosslinked 3 x 400mJ, 254nm
Extracted molecule total RNA
Extraction protocol FMRP-IP, proteinase K, phenol:chloroform extraction
CleanTag Ligation Kit for Small RNA Library Prep (trilink)
 
Library strategy RIP-Seq
Library source transcriptomic
Library selection other
Instrument model Ion Torrent Proton
 
Description fragments_count_table.txt
Data processing Reads adaptor trimming with cutapdapt (v1.2.1). Proton 5’ adapter sequence (--front = TTCTACAGTCCGACGATC). Proton 3’ adapter sequence (--adapter = TGGAATTCTCGGGTGCCAAGG) and SOLiD 3' adapter sequence(--adapter=33020103).
Trimmed reads with a length under 20 bases were discarded.
Remaining reads were aligned with bowtie (version 0.12.7) directly to refseq transcriptome downloaded from NCBI ftp server (release 20161019) with “--best --strata --norc”.
Reads mapped to more than one unique gene were discard with a custom java class based on Picard java API.
Alignment files were filtered to discards PCR duplicates by keeping only one read per alignment start position taking into account possible stretch of soft clipped bases at the 5’ of the reads.
Resulting reads are called fragments and represent the signal of our CLIP experiments aiming at the detection of the FMRP binding sites.
Genome_build: mm10
Supplementary_files_format_and_content: Fragments counts per sample and per gene.
 
Submission date Sep 26, 2017
Last update date May 15, 2019
Contact name Kevin Lebrigand
Organization name IPMC/CNRS
Lab Functional Genomics Platform of Nice-Sophia-Antipolis, France.
Street address 660 route des lucioles
City Valbonne - Sophia-Antipolis
ZIP/Postal code 06560
Country France
 
Platform ID GPL18635
Series (1)
GSE104269 Modulation of synaptic phosphodiesterase PDE2A activity is a new therapeutic approach for Fragile X Syndrome in newborns and adolescents.
Relations
BioSample SAMN07702820
SRA SRX3217320

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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