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Sample GSM2471496 Query DataSets for GSM2471496
Status Public on May 10, 2017
Title e9.5 AVC Hand2 wt (3)
Sample type SRA
 
Source name e9.5 AVC Hand2 wt
Organism Mus musculus
Characteristics stain background: Outbred NMRI mice
genotype/variation: wild type
developmental stage: gestational day e9.0-e9.25
tissue: embryonic heart
tissue: Atrioventricular canal tissue
library type: Unstranded
Growth protocol The Hand2 d/d (null-Mutant) allele was generated by Cre-mediated deletion of the entire Hand2 coding regions in the germline (PMID: 20386744). Noon of the day the vaginal plug was observed was considered as embryonic day 0.5 (E0.5). Mice and embryos were genotyped by PCR using genomic DNA extracted from toe biopsies and yolk sacs, respectively.
Extracted molecule total RNA
Extraction protocol Atrioventricular canals were hand-dissected from isolated hearts using Tungsten needles, flash-frozen individually in Qiagen RTL buffer and stored at -80 °C until genotyped. For each genotype, four replicates of four pooled AVCs with the same distribution of somite stages and sex ratios were prepared and RNA was extracted using Qiagen RNeasy Micro kit according to the manufacturer's protocol."
The quality of total RNA (30-60ng) from the four wild-type and Hand2-deficient samples was analyzed using the RNA 6000 Pico kit in combination with the Agilent 2100 Bioanalyzer. Seven of the eight samples had RIN values >=8.5, while the RNA extracted from one wild-type sample was of suboptimal quality. Therefore, only three wild-type and all four Hand2-deficient samples were processed for sequencing. Ribosomal RNA was depleted using the Ribo-Zero Magnetic Gold Kit (Epicentre). RNA-Seq libraries were prepared using the Clontech SMARTer Low Input RNA kit (Clontech). The resulting cDNA was subjected to eight cycles of PCR amplification and sequenced on a Illumina HiSeq 3000 instrument with a SR50 protocol.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 3000
 
Description e9.5_AVC_Hand2_wt_rep3
Data processing Reads were aligned to the mm9 reference genome and to the Mus Musculus transcriptome (iGenome refGene) using TopHat v2.0.13 (PMID: 23618408). The option --no-coverage-search was specified, while all the other parameters were left to default.
Gene-wise counts were calculated using htseq-count (PMID: 25260700) setting -s to no and considering the same reference transcriptome. Only those reads with a unique match to the genome were considered (samtools view -q1).
Genome_build: mm9 (NCBI Build 37), transcripts from Mus Musculus Ensembl Build 63.
Supplementary_files_format_and_content: *.counts.txt list the raw counts per gene as inferred by htseq-count.
 
Submission date Jan 27, 2017
Last update date May 15, 2019
Contact name Iros Barozzi
E-mail(s) iros.barozzi@meduniwien.ac.at
Organization name Medical University Vienna
Street address Borschkegasse 8a
City Vienna
ZIP/Postal code 1090
Country Austria
 
Platform ID GPL21493
Series (1)
GSE94246 HAND2 Target Gene Regulatory Networks Control Cardiac Valve Development
Relations
BioSample SAMN06277531
SRA SRX2524490

Supplementary file Size Download File type/resource
GSM2471496_e9.5_AVC_Hand2_wt.3.counts.txt.gz 97.3 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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