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Series GSE206559 Query DataSets for GSE206559
Status Public on Jan 13, 2023
Title Loss of CPSF6 causes developmental disease via bimodal changes in polyadenylation site usage and protein expression
Organisms Danio rerio; Homo sapiens
Experiment type Other
Summary This SuperSeries is composed of the SubSeries listed below.
 
Overall design Refer to individual Series
 
Citation(s)
  • de Prisco N, Ford C, Elrod ND, Lee W et al. Alternative polyadenylation alters protein dosage by switching between intronic and 3'UTR sites. Sci Adv 2023 Feb 17;9(7):eade4814. PMID: 36800428
Submission date Jun 21, 2022
Last update date Feb 23, 2023
Contact name Hari Krishna Yalamanchili
E-mail(s) hari.yalamanchili@bcm.edu
Organization name Baylor College of Medicine
Street address 1250 Moursund St #1125,
City Houston,
State/province TX
ZIP/Postal code 77030
Country USA
 
Platforms (2)
GPL21697 NextSeq 550 (Homo sapiens)
GPL21741 Illumina HiSeq 4000 (Danio rerio)
Samples (29)
GSM6256850 CPSF6-DEL-1_S4
GSM6256851 CPSF6-DEL-2_S5
GSM6256852 CPSF6-DEL-3_S6
This SuperSeries is composed of the following SubSeries:
GSE206557 Loss of CPSF6 causes developmental disease via bimodal changes in polyadenylation site usage and protein expression [Human]
GSE206558 Loss of CPSF6 causes developmental disease via bimodal changes in polyadenylation site usage and protein expression [Zebrafish]
Relations
BioProject PRJNA851372

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
GSE206559_RAW.tar 1.3 Gb (http)(custom) TAR (of BW)
SRA Run SelectorHelp

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