Sign in to NCBI

Display Settings:

Format

Send to:

Choose Destination
Accession: PRJNA336351 ID: 336351

DHX9 suppresses spurious RNA processing defects originating from the Alu invasion of the human genome [uvCLAP CLIP-seq]

Navigate Up
This project is a component of the DHX9 suppresses spurious RNA processing defects originating from the Alu invasion of the human genome
Navigate Across
5 additional projects are components of the DHX9 suppresses spurious RNA processing defects originating from the Alu invasion of the human genome.
Transposable elements increase genetic diversity thus making them an important part of evolution and gene regulation in all organisms that carry these sequences. More...
AccessionPRJNA336351; GEO: GSE85155
ScopeMultispecies
PublicationsAktaş T et al., "DHX9 suppresses RNA processing defects originating from the Alu invasion of the human genome.", Nature, 2017 Apr 6;544(7648):115-119
SubmissionRegistration date: 3-Aug-2016
Akhtar Lab, Chromatin Regulation, Max Planck Institute of Immunobiology and Epigenetics
RelevanceUnknown
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments52
Publications
PubMed1
Other datasets
BioSample52
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Supplementary Mbytes579
SRA Data Details
ParameterValue
Data volume, Gbases79
Data volume, Mbytes35391

Supplemental Content

Related information

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
You are here: NCBI
Support Center