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Series GSE137335 Query DataSets for GSE137335
Status Public on Oct 25, 2020
Title Non-coding deletions identify Maenli lncRNA as a limb-specific En1 regulator
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Genome binding/occupancy profiling by high throughput sequencing
Other
Summary This SuperSeries is composed of the SubSeries listed below.
 
Overall design Refer to individual Series
Web link https://doi.org/10.1038/s41586-021-03208-9
 
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Submission date Sep 12, 2019
Last update date Feb 09, 2021
Contact name Lila Allou
Organization name Max Planck Institute For Molecular Genetics
Department FG Development and Disease
Lab FG Mundlos
Street address 63-73 Ihnestrasse
City Berlin
ZIP/Postal code 14195
Country Germany
 
Platforms (2)
GPL17021 Illumina HiSeq 2500 (Mus musculus)
GPL21103 Illumina HiSeq 4000 (Mus musculus)
Samples (70)
GSM4075506 FL-E95-WT-Mm9-Rep1-PolyA-RNAseq-L10170
GSM4075508 FLHL-E115-3xpA-Mm9-Rep1-ATAC-L17218
GSM4075509 FLHL-E115-3xpA-Mm9-Rep2-ATAC-L17219
This SuperSeries is composed of the following SubSeries:
GSE137329 Loss of Maenli lncRNA expression causes engrailed-1 dependent congenital limb malformations [RNA-seq]
GSE137330 Loss of Maenli lncRNA expression causes engrailed-1 dependent congenital limb malformations [ATAC-seq]
GSE137331 Loss of Maenli lncRNA expression causes engrailed-1 dependent congenital limb malformations [ChIP-seq]
Relations
BioProject PRJNA565194

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE137335_RAW.tar 3.4 Gb (http)(custom) TAR (of BED, BW)
SRA Run SelectorHelp

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