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Data Analysis on a dataset of normalized RNA Sequencing reads for pancreatic cancer tumors​

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Pancreatic Adenocarcinoma

Pancreatic Adenocarcinoma (PAAD) is the third most common cause of death from cancer, with an overall 5-year survival rate of less than 5%, and is predicted to become the second leading cause of cancer mortality in the United States by 2030.

Here we had a dataset of normalized RNA Sequencing reads for pancreatic cancer tumors. The measurement consists of ~20,000 genes for 185 pancreatic cancer tumors.

Data cleaning and check the distribution of gene expression across samples

  • Read data from GCT file, a tab-delimited file used for sharing gene expression data and metadata (details for each sample) for samples.
  • Remove genes with NaNs
  • Generate gene expression distribution for all samples.

Identifying the Exocrine(adenocarcinoma) tumors and remove Neuroendocrine tumors

  • Visualize the data whole data using PCA and analyze the variance of PCA
  • Analyse the general behavior of the different samples
  • Remove the neuroendocrine tumors from the dataset so that it contains only the adenocarcinoma tumor samples

Understand the effect of Interferons in Pancreatic Adenocarcinoma and Unsupervised analysis

  • Plot the gene expression values for these genes for pancreatic adenocarcinoma
  • Unsupervised clustering on the gene expression data

Refferences

EDA on Titanic dataset

Dimensionality Reduction

Unsupervised Clustering Algorithms

If Github shows an error while loading the notebook please view it on nbviewer by Jupyter here

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Data Analysis on a dataset of normalized RNA Sequencing reads for pancreatic cancer tumors​

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