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Sample GSM4417291 Query DataSets for GSM4417291
Status Public on Sep 17, 2020
Title Pm_mantle_a
Sample type SRA
 
Source name mantle tissue of the King Scallop
Organism Pecten maximus
Characteristics tissue: mantle
Extracted molecule total RNA
Extraction protocol Cells were disrupted manually with a pestle in liquid nitrogen before RNA extraction using RNeasy universal kit (Qiagen).
Libraries were made at the Wellcome Sanger Institute. These were made according to their autoRNA library preparation process, with poly(A) pulldown, fragmentation, 1st and 2nd strand synthesis, end prep and ligation using the NEB Ultra II RNA custom kit (New England Biolabs, Massachusetts, United States) on an Agilent Bravo WS automation system (Agilent, California, United States). 14 rounds of PCR were used in library construction.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2000
 
Data processing Initial trimming of poor quality sequence and residual Illumina adaptors with TrimGalore v0.6 at default parameters.
Reads were mapped using STAR 2.7 with the --quantMode GeneCounts option to a genome library of xPecMax.fa (produced using --sjdbOverhang 149)
Genome_build: GCA_902652985.1
Supplementary_files_format_and_content: Tab-delimtied STAR output of read counts
 
Submission date Mar 17, 2020
Last update date Sep 18, 2020
Contact name Katherine James
E-mail(s) [email protected]
Organization name Newcastle University
Department School of Computing
Street address Urban Sciences Building
City Newcastle upon Tyne
ZIP/Postal code NE1 7RU
Country United Kingdom
 
Platform ID GPL28284
Series (1)
GSE147107 RNA-seq of scallop mantle tissue
Relations
BioSample SAMN14390692
SRA SRX7924984

Supplementary file Size Download File type/resource
GSM4417291_read_counts_Pm_mantle_a.tab.gz 800.1 Kb (ftp)(http) TAB
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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