|
Status |
Public on Mar 16, 2015 |
Title |
SMO variants explain the majority of drug resistance in basal cell carcinoma |
Organism |
Homo sapiens |
Experiment type |
Other Expression profiling by high throughput sequencing
|
Summary |
This SuperSeries is composed of the SubSeries listed below.
|
|
|
Overall design |
Refer to individual Series
|
|
|
Citation(s) |
25759020 |
Submission date |
Jun 10, 2014 |
Last update date |
May 15, 2019 |
Contact name |
Jiang Li |
E-mail(s) |
jiangli@stanford.edu
|
Phone |
6507258839
|
Organization name |
Stanford University
|
Department |
Dermatology
|
Lab |
Tony Oro
|
Street address |
269 Campus Drive, Stanford University
|
City |
Stanford |
State/province |
CA |
ZIP/Postal code |
94305 |
Country |
USA |
|
|
Platforms (2) |
GPL15520 |
Illumina MiSeq (Homo sapiens) |
GPL16791 |
Illumina HiSeq 2500 (Homo sapiens) |
|
Samples (107)
|
|
This SuperSeries is composed of the following SubSeries: |
GSE58374 |
SMO variants explain the majority of drug resistance in basal cell carcinoma [exome-seq] |
GSE58375 |
SMO variants explain the majority of drug resistance in basal cell carcinoma [RNA-Seq] |
GSE58376 |
SMO variants explain the majority of drug resistance in basal cell carcinoma [Target Sequencing] |
|
Relations |
BioProject |
PRJNA252374 |