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SRX1118955: Deep hyper saline anoxic basin sediments
1 ILLUMINA (Illumina HiSeq 2000) run: 14M spots, 4.2G bases, 3.1Gb downloads

Design: After confirming the absence of DNA, the Ovation Single Cell RNA-seq kit (Nugen, San Carlos, CA) was used to create barcoded cDNA libraries for sequencing. A modified step was followed in which the First Strand Primer Mix, A1 ver 15 (S01882) was replaced with the First Strand Primer Mix, A1 ver 13 (S01858) to avoid biases against prokaryotic transcripts. The libraries were sequenced at DNA Sequencing & Genotyping Center, University of Delaware using Illumina HiSeq platform and paired-end 150 run. The five libraries were pooled in 3 lanes. The forward and reverse reads were filtered using Trimmomatic. The length of the trimmed sequences was set to be at least 50 nt. Surviving trimmed reads were used for assembly with Trinity release r20140717.
Submitted by: Woods Hole Oceanographic Institution
Study: Deep Hypersaline Anoxic Basins Transcriptome or Gene expression
show Abstracthide Abstract
This project aims to describe the overall picture of transcribed genes from microorganisms (all 3 domains of life) in sediments underlying the halo clines (transition zones between normal salinity deep mediterranean Sea and brine) of several deep hyper saline anoxic basins in the E. Mediterranean Sea. Average depth is ~3500m or greater. Also some nearby normal salinity core samples were collected around 10m outside the influence of the brines. Analyses are based on top ~3cm of the sediments
Sample: UC
SAMN03760857 • SRS1011626 • All experiments • All runs
Library:
Name: UraniaBasinControlSediments
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: METATRANSCRIPTOMIC
Selection: RANDOM
Layout: PAIRED
Spot descriptor:
forward152  reverse

Runs: 1 run, 14M spots, 4.2G bases, 3.1Gb
Run# of Spots# of BasesSizePublished
SRR254201013,993,8794.2G3.1Gb2016-01-01

ID:
1632960

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