Genomics

Dataset Information

0

Multimodal epigenetic changes and altered NEUROD1 chromatin binding in the mouse hippocampus underlie FOXG1 syndrome

ABSTRACT: Multimodal epigenetic changes and altered NEUROD1 chromatin binding in the mouse hippocampus underlie FOXG1 syndrome

PROVIDER: PRJNA781588 | ENA |

REPOSITORIES: ENA

Json Xml

Dataset's files

Source:
Action DRS
SRR16975362_1.fastq.gz Fastqsanger.gz
SRR16975362_2.fastq.gz Fastqsanger.gz
SRR16975363_1.fastq.gz Fastqsanger.gz
SRR16975363_2.fastq.gz Fastqsanger.gz
SRR16975364_1.fastq.gz Fastqsanger.gz
Items per page:
1 - 5 of 8

Similar Datasets

Genomics Multimodal epigenetic changes and altered NEUROD1 chromatin binding in the mouse hippocampus underlie FOXG1 syndrome
2023-01-09 | GSE189110 | GEO
Genomics Multimodal epigenetic changes and altered NEUROD1 chromatin binding in the mouse hippocampus underlie FOXG1 syndrome
| PRJNA781594 | ENA
Genomics Multimodal epigenetic changes and altered NEUROD1 chromatin binding in the mouse hippocampus underlie FOXG1 syndrome
| PRJNA781589 | ENA
Genomics Multimodal epigenetic changes and altered NEUROD1 chromatin binding in the mouse hippocampus underlie FOXG1 syndrome
| PRJNA781595 | ENA
Genomics Multimodal epigenetic changes and altered NEUROD1 chromatin binding in the mouse hippocampus underlie FOXG1 syndrome
| PRJNA781591 | ENA
Genomics Multimodal epigenetic changes and altered NEUROD1 chromatin binding in the mouse hippocampus underlie FOXG1 syndrome
| PRJNA781585 | ENA
Genomics Multimodal epigenetic changes and altered NEUROD1 chromatin binding in the mouse hippocampus underlie FOXG1 syndrome
| PRJNA781593 | ENA
Genomics Multimodal epigenetic changes and altered NEUROD1 chromatin binding in the mouse hippocampus underlie FOXG1 syndrome
| PRJNA781590 | ENA
Genomics Multimodal epigenetic changes and altered NEUROD1 chromatin binding in the mouse hippocampus underlie FOXG1 syndrome
| PRJNA781592 | ENA
Genomics Multimodal epigenetic changes and altered NEUROD1 chromatin binding in the mouse hippocampus underlie FOXG1 syndrome
2023-01-09 | GSE189115 | GEO