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SRX3015369: GSM2710825: total RNA-seq in Testis [VT_RNA-seq]; Drosophila virilis; RNA-Seq
1 ILLUMINA (Illumina HiSeq 1000) run: 87.7M spots, 13.1G bases, 8.3Gb downloads

Submitted by: NCBI (GEO)
Study: Landscape and evolution of tissue-specific alternative polyadenylation across Drosophila species
show Abstracthide Abstract
we generated developmental and tissue-specific 3'-seq libraries from D. yakuba and D. virilis to study the role of alternative polyadenylation across Drosophila species Overall design: Deep 3'-sequencing data from 23 developmental stages, tissues and cell lines of D. melanogaster, D.yakuba, and D. virilis Please note that 23 refer to # samples in Drosophila melanogaster. D. yakuba and D. virillis samples were used to study species homology in the paper, which are from the same tissue type as D. melanogaster.
Sample: total RNA-seq in Testis [VT_RNA-seq]
SAMN07367979 • SRS2365028 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 1000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: 3'-seq libraries were prepared and sequenced as described (Sanfilippo P, Miura P, Lai EC: Genome-wide profiling of the 3' ends of polyadenylated RNAs. Methods 2017, 75:in press.), using 2 μg of total RNA as starting material. Total RNA-seq libraries were prepared starting with 1 μg of total RNA in water. The 3p-seq libraries were sequenced using a hiseq-1000 with SE-50 mode at the genomics core facility at MSKCC. Total RNA-seq libraries were prepared using the Illumina TruSeq Stranded Total RNA Library Prep Kit (cat. No. RS-122-2201). The protocol was followed exactly as per manufacturer's instructions. The libraries were sequenced on a hiseq-1000 sequencer at the genomics core facility at MSKCC. 3p-seq hiseq-1000 with SE-50; Total RNA-seq paired-end PE75
Experiment attributes:
GEO Accession: GSM2710825
Links:
Runs: 1 run, 87.7M spots, 13.1G bases, 8.3Gb
Run# of Spots# of BasesSizePublished
SRR583944387,664,69013.1G8.3Gb2017-11-02

ID:
4289661

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