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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
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|
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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
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|
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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 |