Master Analysis of Microarray Data using Machine Learning/AI in R in 4 weeks through hands-on, project-based online training with DSTC.
Microarrays are one of the most common tools to understand biological spectacle by large-scale dimensions of biological samples, typically DNA, RNA, or proteins. The technique has been used for a variety of purposes in life science research, ranging from gene expression profiling to SNP or other biomarker identification, and further, to understand relations between genes and their activities on a large scale. Artificial intelligence (AI) and machine learning (ML) techniques can be used to analyse microarray data to gain insights into biological processes. Every participant receives a verified e-Certificate and e-Marksheet from the Deep Science & Technology Consortium.
Microarrays are one of the most common tools to understand biological spectacle by large-scale dimensions of biological samples, typically DNA, RNA, or proteins. The technique has been used for a variety of purposes in life science research, ranging from gene expression profiling to SNP or other biomarker identification, and further, to understand relations between genes and their activities on a large scale. Artificial intelligence (AI) and machine learning (ML) techniques can be used to analyse microarray data to gain insights into biological processes.
1. Put biotechnology techniques to work on real datasets and case studies.
2. Produce a reproducible, portfolio-ready project you can cite in a thesis, paper, or job application.
β’ Master's and senior undergraduate students specializing in biotechnology
β’ R&D engineers and working professionals applying biotechnology in industry
β’ Academics and educators building research or teaching capacity in biotechnology
β’ A portfolio-grade biotechnology deliverable you can defend and extend.
β’ A verified e-Certificate of competency and e-Marksheet from the Deep Science & Technology Consortium.
β’ Affymetrix, Illumina and two-colour platforms and the differences that matter
β’ CEL files, probe-to-gene mapping and multi-probe genes
β’ Retrieving and reading experiments from GEO with GEOquery
β’ Background correction, RMA normalisation and quantile normalisation in affy and oligo
β’ Array quality assessment and the defensible grounds for excluding an array
β’ Batch effect detection by PCA before any modelling is attempted
β’ limma, the linear model framework and empirical Bayes moderation
β’ Design and contrast matrices for anything beyond a two-group comparison
β’ FDR control and why an unadjusted p-value list is not a result
β’ Classification with caret or tidymodels when features vastly outnumber samples
β’ Feature selection inside the resampling loop, or the accuracy is inflated
β’ Clustering, heatmaps and the arbitrariness of the chosen distance metric
β’ Over-representation against GSEA and the correct background gene set
β’ Validation in an independent GEO dataset as the honest check
β’ Where microarray conclusions do and do not agree with RNA-Seq
| Parameter | Requirement |
|---|---|
| Covered Tool / Platform | Python |
| Covered Tool / Platform | Scikit-learn |
| Covered Tool / Platform | TensorFlow |
| Covered Tool / Platform | Keras |
| Covered Tool / Platform | Pandas |
| Covered Tool / Platform | NumPy |
| Covered Tool / Platform | Matplotlib |
| Covered Tool / Platform | XGBoost |
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