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Status |
Public on Jun 17, 2024 |
Title |
Skin_congenital_melanocytic_nevus_patient_CMN16 |
Sample type |
genomic |
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Source name |
Skin
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Organism |
Homo sapiens |
Characteristics |
tissue: Skin cell type: Melanocyte, keratinocyte, fibroblast cells, others genotype: NRAS Q61R treatment: None
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Treatment protocol |
None
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Extracted molecule |
genomic DNA |
Extraction protocol |
DNA was extracted from flash-frozen biopsies or paraffin blocks using standard salting-out techniques.
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Label |
Cy3 and Cy5
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Label protocol |
Bisulfite treatment was carried out to convert 500 ng of DNA into unmethylated cytosine nucleotides to uracil using the EpiJET Bisulfite Conversion Kit (ThermoFisher Scientific).
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Hybridization protocol |
DNAs were hybridized to an Infinium Methylation EPIC v1 BeadChip arrays (Illumina)
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Scan protocol |
Scanned using an Illumina iSCAN platform.
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Data processing |
Preprocessing and quality control of the sample intensity data (IDAT) files were performed using the R package Minfi package (v.1.48.0). Sample normalization was done with the preprocessQuantile function. Once our data was combined with publicly available datasets (GSE188593), cell-type deconvolution was performed using the Epidish function, and using a reference library for DNA methylation-based cell-type deconvolution containing melanocyte, keratinocyte, and fibroblast cells. After filtering, normalization, and deconvolution differentially methylated probes were identified through mixed linear regression models using a Limma package from R.
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Submission date |
May 31, 2024 |
Last update date |
Oct 02, 2024 |
Contact name |
Daniel Aldea |
E-mail(s) |
daniel.ALDEA-ARIAS@univ-amu.fr
|
Organization name |
Aix-Marseille University
|
Street address |
27 Bd Jean Moulin
|
City |
Marseille |
ZIP/Postal code |
13385 |
Country |
France |
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Platform ID |
GPL21145 |
Series (1) |
GSE268769 |
Deconvoluted methylation profiles discriminate between closely related melanocytic nevi |
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