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Links from GEO DataSets

Items: 9

1.

RecG Directs DNA Synthesis During Double-Strand Break Repair

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Escherichia coli
Type:
Genome binding/occupancy profiling by high throughput sequencing; Other
Platform:
GPL14548
27 Samples
Download data: BEDGRAPH
Series
Accession:
GSE77184
ID:
200077184
2.

RecG Directs DNA Synthesis During Double-Strand Break Repair [Chromosomal marker frequency analysis]

(Submitter supplied) In the bacterium Escherichia coli, RecG directs DNA synthesis during the repair of DNA double-strand breaks by homologous recombination.
Organism:
Escherichia coli
Type:
Other
Platform:
GPL14548
23 Samples
Download data: TXT
Series
Accession:
GSE77183
ID:
200077183
3.

RecG Directs DNA Synthesis During Double-Strand Break Repair [ChIP-seq]

(Submitter supplied) In the bacterium Escherichia coli, RecG directs DNA synthesis during the repair of DNA double-strand breaks by homologous recombination.
Organism:
Escherichia coli
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL14548
4 Samples
Download data: BEDGRAPH
Series
Accession:
GSE77181
ID:
200077181
4.

Genomic Analysis of DNA Double-Strand Break Repair in Escherichia coli (MFA profiles)

(Submitter supplied) Counting DNA reads using whole genome sequencing is providing new insight into DNA double-strand break repair (DSBR) in the model organism Escherichia coli. We describe the application of RecA chromatin immunoprecipitation coupled to genomic DNA sequencing (RecA-ChIP-seq) and marker frequency analysis (MFA) to analyse the genomic consequences of DSBR.
Organism:
Escherichia coli
Type:
Genome binding/occupancy profiling by high throughput sequencing; Other
Platforms:
GPL25368 GPL18133
24 Samples
Download data: CSV, FASTA
Series
Accession:
GSE117952
ID:
200117952
5.

Genomic Analysis of DNA Double-Strand Break Repair in Escherichia coli

(Submitter supplied) Counting DNA reads using whole genome sequencing is providing new insight into DNA double-strand break repair (DSBR) in the model organism Escherichia coli. We describe the application of RecA chromatin immunoprecipitation coupled to genomic DNA sequencing (RecA-ChIP-seq) and marker frequency analysis (MFA) to analyse the genomic consequences of DSBR.
Organism:
Escherichia coli
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL25368
8 Samples
Download data: CSV, FASTA
Series
Accession:
GSE117541
ID:
200117541
6.

RecBCD Coordinates Repair of Two Ends at a DNA Double-Strand Break, Preventing Aberrant Chromosome Amplification

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Escherichia coli K-12
Type:
Genome binding/occupancy profiling by high throughput sequencing; Other
Platforms:
GPL19529 GPL24377
18 Samples
Download data: CSV, TXT
Series
Accession:
GSE107974
ID:
200107974
7.

RecBCD Coordinates Repair of Two Ends at a DNA Double-Strand Break, Preventing Aberrant Chromosome Amplification [MFA]

(Submitter supplied) The effect of an induced site-specific DNA double-strand break on DNA abundance across the chromosome of E. coli cells expressing or not RecD protein, was investigated by marker frequency analysis.
Organism:
Escherichia coli K-12
Type:
Other
Platform:
GPL19529
10 Samples
Download data: CSV, FASTA
Series
Accession:
GSE107973
ID:
200107973
8.

RecBCD Coordinates Repair of Two Ends at a DNA Double-Strand Break, Preventing Aberrant Chromosome Amplification [ChIP-seq]

(Submitter supplied) In the bacterium Escherichia coli, RecBCD coordinates repair of two ends at a DNA double-strand break, preventing aberrant chromosome amplification
Organism:
Escherichia coli K-12
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL24377 GPL19529
8 Samples
Download data: CSV, FASTA, TXT
Series
Accession:
GSE107972
ID:
200107972
9.

Avoiding chromosome pathology when replication forks collide

(Submitter supplied) Chromosome duplication normally initiates via the assembly of replication fork complexes at defined origins. DNA synthesis by any one fork is thought to cease when it meets another travelling in the opposite direction, at which stage the replication machinery may simply dissociate before the nascent strands are finally ligated. But what actually happens is not clear. Here we present evidence consistent with the idea that every fork collision has the potential to trigger re-replication of the already replicated DNA, thus posing a threat to genomic integrity. more...
Organism:
Escherichia coli
Type:
Other
Platform:
GPL16232
33 Samples
Download data: TXT, WIG
Series
Accession:
GSE41975
ID:
200041975
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Supplemental Content

db=gds|term=|query=1|qty=3|blobid=MCID_679dc60e55a6950b4d66871d|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
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