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SRX25641102: RAD-seq of Pacific Oyster: Molluscan Broodstock Program, Oregon State University
1 ION_TORRENT (Ion Torrent Proton) run: 1.9M spots, 154.2M bases, 106.5Mb downloads

Design: DNA was extracted from adductor muscle sections of Crassostrea gigas, purified and quantified by fluorometry, then normalized to 10 ng/ul and used as an input to double-digest restriction site associated (RAD)-sequencing library preparation. Genomic DNA was digested using NsiI and MspI cutting enzymes, and size selected. Samples were individually barcoded and multiplexed at 32 individuals per chip. Multiplexed libraries were sequenced on an Ion Torrent Proton. Fastq data were trimmed for adapters and low quality sequences, then demultiplexed and truncated to a consistent size (80 bp), then uploaded to NCBI.
Submitted by: Vancouver Island University
Study: Selection of Pacific oysters using an OsHV-1 resistance marker has no influence on susceptibility to Vibrio aestuarianus
show Abstracthide Abstract
Reduced representation sequencing (double-digest restriction site-associated DNA sequencing) dataset to support a genome-wide association study of survival to a Vibrio aestuarianus infection in a selectively-bred population of Pacific oyster for viral resistance.
Sample: 188
SAMN43080898 • SRS22285365 • All experiments • All runs
Organism: Magallana gigas
Library:
Name: F115-Dead_188
Instrument: Ion Torrent Proton
Strategy: RAD-Seq
Source: GENOMIC
Selection: Reduced Representation
Layout: SINGLE
Runs: 1 run, 1.9M spots, 154.2M bases, 106.5Mb
Run# of Spots# of BasesSizePublished
SRR301747711,927,329154.2M106.5Mb2024-11-21

ID:
34655679

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