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Sample GSM5284932 Query DataSets for GSM5284932
Status Public on Nov 25, 2021
Title siDis3l2-2cell-Rep2 [50]
Sample type SRA
 
Source name siDis3l2-2cell
Organism Mus musculus
Characteristics stain: C57BL/6
genotype/variation: siDis3l2
developmental stage: 2Cell embryo
Treatment protocol Samples were collected with 0.2% BSA in DPBS at indicated time directly without extra treatment.
Growth protocol The embyos are clutured in KSOM in vitro.
Extracted molecule total RNA
Extraction protocol Embryos were collected from indicated genotypes (10 embryos per sample). Each sample was directly lysed with 4.2 ul lysis buffer (0.2% Triton X-100, RNase inhibitor, dNTPs, oligo-dT primers, and 1:1000 ERCC spike-in) and immediately used for cDNA synthesis using the Smart-seq2 method as described previously (Picelli et al, 2014).
Sequencing libraries were constructed from 500 pg of amplified cDNA using TruePrep DNA Library Prep Kit V2 for Illumina (Vazyme, TD503) according to manufacturer’s instructions. Barcoded libraries were pooled and sequenced on the Illumina HiSeq X Ten platform with 150 bp paired-end reads
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model HiSeq X Ten
 
Description processed data file: siDis3l2-FPKM.txt
Data processing RNA-Seq was performed with biological replicates for all samples. Raw reads were trimmed to 50 bp and mapped to the mouse genome (mm9) and ERCC spike-in sequences with Tophat v2.1.1. Only uniquely mapped reads were subsequently assembled into transcripts guided by the reference annotation (UCSC gene models) with Cufflinks v2.2.1. Expression level of each gene was quantified with normalized FPKM (fragments per kilobase of exon per million mapped fragments) and was further normalized with the ERCC spike-in. Samples prepared in different batches were normalized by the zygote sample in each batch.
Genome_build: mm9
Supplementary_files_format_and_content: Tab-delimited text files include FPKM values of all RNA-seq samples
 
Submission date May 07, 2021
Last update date Nov 25, 2021
Contact name Heng-yu Fan
E-mail(s) Fanhengyu_lab@163.com, 21907079@zju.edu.cn
Organization name Life Sciences Institute
Lab Fan heng-yu
Street address Yuhangtang Road
City Hangzhou
State/province Zhejiang
ZIP/Postal code 310058
Country China
 
Platform ID GPL21273
Series (1)
GSE174032 Nuclear Poly(A) Binding Protein 1 (PABPN1) Mediates Zygotic Genome Activation-dependent Maternal mRNA Clearance During Mouse Early Embryonic Development
Relations
BioSample SAMN19066885
SRA SRX10813719

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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