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SRX011007: Aglantha digitale transcriptome
1 LS454 (454 GS FLX) run: 7,126 spots, 1.2M bases, 2.9Mb downloads

Design: Total RNA is extracted from one Aglantha digitale. Library construction starts with total RNA reverse transcribed to cDNA with an oligo dT primer, with second strand then generated. The cDNA is digested with a restriction enzyme then adaptors ligated onto the double-stranded (ds) DNA. The adaptor ligated cDNA fragments are the amplified by PCR. This product is purified and processed for emPCR and 454 sequencing according to manufactures procedures.
Submitted by: University of Florida - Leonid Moroz (UF-LM)
Study: Aglantha digitale transcriptome
show Abstracthide Abstract
The Pacific hydromedusa Aglantha is an important model organism to study earlier stages of the evolution and organization of neural circuits and behavior. However, nothing is known about the molecular organization of this organism. Here, using pyrosequencing approach we initiated transcriptome analysis of this emerging model. Specifically, we developed a reduced representation sequencing method that can detect low abundant transcripts. Our method greatly reduces the amount of sequencing with more accurate quantification. Basically, sequential addition of adaptors paired with controlled digestion of cDNA generates a one transcript on read type of analysis. Combined 5’ with 3’ targeted libraries produces greater coverage of individual transcripts and high quality assembly. Our initial analysis allowed us to identify more than 2,000 of novel transcripts including many components of signal transduction pathways essential for future analysis of molecular bases of neuronal functions in this model organism
Sample: Generic sample from Aglantha digitale
SAMN00003351 • SRS005624 • All experiments • All runs
Library:
Name: Ad
Instrument: 454 GS FLX
Strategy: AMPLICON
Source: TRANSCRIPTOMIC
Selection: RANDOM
Layout: SINGLE
Spot descriptor:
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Runs: 1 run, 7,126 spots, 1.2M bases, 2.9Mb
Run# of Spots# of BasesSizePublished
SRR0271467,1261.2M2.9Mb2015-02-21

ID:
11294

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