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SRX3202739: GSM2789281: AM16144_Scc1-6HA_CEN3del_no_tension_input; Saccharomyces cerevisiae; ChIP-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 15.3M spots, 779.1M bases, 495.7Mb downloads

Submitted by: NCBI (GEO)
Study: Scc1 ChIP-Seq in a strain where the centromere on chromosome III has been moved to an ectopic site
show Abstracthide Abstract
Genome binding/occupancy profiling of the cohesin subunit Scc1 by high throughput sequencing Overall design: Purpose: Can the centromere set up new pericentromere borders on a chromosomal arm site?
Sample: AM16144_Scc1-6HA_CEN3del_no_tension_input
SAMN07679846 • SRS2529240 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2000
Strategy: ChIP-Seq
Source: GENOMIC
Selection: ChIP
Layout: SINGLE
Construction protocol: Input and ChIP DNA were sent for sequencing. All samples were prepared using a liquid handling robot (Hamilton) by Bianka Baying (EMBL, Heidelberg, Germany). 10ng of each sample mixed with library preparation were assessed according to manufacturer's recommendation (NEBNext Ultra™ DNA Library Prep Kit for Illumina, (#E7370S/L)). Library preparation was done according to manufacturer. Briefly, the Adapter in the Adapter Ligation step was diluted 1:30 in water. The size selection step was performed with Ampure XP Beads from Beckman Coulter (insert size 200-250bp). The PCR amplification was performed in 15 cycles. Finally NEBNext Multiplex Oligos for Illumina (Index Primer Set 1) (#E7335S/L) were used for the Indexing. The quality and quantity of the libraries was checked using the Agilent BioAnalyzer and the Qubit dsDNA HS Assay kit (Invitrogen). ChIP-Seq was performed using Illumina HiSeq 2000 Sequencer with Requested Read Length HiSeq50 SE.
Experiment attributes:
GEO Accession: GSM2789281
Links:
Runs: 1 run, 15.3M spots, 779.1M bases, 495.7Mb
Run# of Spots# of BasesSizePublished
SRR605581015,275,580779.1M495.7Mb2020-01-15

ID:
4508292

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