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Status |
Public on Nov 22, 2024 |
Title |
Aberrant homeodomain-DNA cooperative dimerization underlies distinct developmental defects in two dominant CRX retinopathy models |
Organisms |
Mus musculus; synthetic construct |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing Other
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Summary |
This SuperSeries is composed of the SubSeries listed below.
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Overall design |
Refer to individual Series
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Citation missing |
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Submission date |
Feb 20, 2024 |
Last update date |
Nov 22, 2024 |
Contact name |
Shiming Chen |
E-mail(s) |
[email protected]
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Phone |
314-747-4351
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Organization name |
Washington University in St Louis
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Department |
Department of Ophthalmology & Visual Sciences
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Lab |
Shiming Chen, Ph.D.
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Street address |
517 South Euclid Avenue
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City |
Saint Louis |
State/province |
Missouri |
ZIP/Postal code |
63110 |
Country |
USA |
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Platforms (2) |
GPL17769 |
Illumina MiSeq (synthetic construct) |
GPL24247 |
Illumina NovaSeq 6000 (Mus musculus) |
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Samples (32)
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This SuperSeries is composed of the following SubSeries: |
GSE256212 |
Aberrant homeodomain-DNA cooperative dimerization underlies distinct developmental defects in two dominant CRX retinopathy models [ATAC-seq] |
GSE256213 |
Aberrant homeodomain-DNA cooperative dimerization underlies distinct developmental defects in two dominant CRX retinopathy models [Coop-seq] |
GSE256214 |
Aberrant homeodomain-DNA cooperative dimerization underlies distinct developmental defects in two dominant CRX retinopathy models [MPRA] |
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Relations |
BioProject |
PRJNA1078421 |