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SRX16838510: PacBio HiFi whole genome sequencing of Tribolium castaneum GA2: adult male
1 PACBIO_SMRT (Sequel II) run: 644,471 spots, 7G bases, 4.3Gb downloads

Design: High molecular weight (HMW) DNA extraction was performed from the whole body using the Qiagen MagAttract HMW DNA Kit. DNA shearing was performed using the Diagenode Megaruptor 2 with the 20 kb fragment protocol. The sheared DNA was prepared for PacBio sequencing using the SMRTBell Express Template kit 2.0. The library was size-selected with beads to remove library molecules less than 3 kb in length to generate the final libraries for sequencing. Sequencing was performed on a Sequel II System using Binding Kit v2.0, Sequencing kit v2.0, and SMRT Cell 8M. To target HiFi reads, the library was sequenced using a 30 hour movie time on one SMRTcell. Raw subreads were converted to HiFi data by processing with CCS to call a single high quality consensus sequence for each molecule, using a 99.5% consensus accuracy cutoff.
Submitted by: United States Department of Agriculture
Study: Genome sequencing of Tribolium castaneum GA2 (red flour beetle) adult male principal pseudohaplotype
show Abstracthide Abstract
Genome sequencing and assembly of Tribolium castaneum GA2 (red flour beetle) was conducted by the USDA-ARS Ag100Pest Initiative. Principal haplotype
Sample: Tribolium castaneum GA2 (red flour beetle)
SAMN30135407 • SRS14443933 • All experiments • All runs
Library:
Name: icTriCast1_PacBio_CCS_low
Instrument: Sequel II
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: SINGLE
Runs: 1 run, 644,471 spots, 7G bases, 4.3Gb
Run# of Spots# of BasesSizePublished
SRR20818908644,4717G4.3Gb2023-09-01

ID:
23601761

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