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    Rnaseq Data Analysis Using Shell Scripting And R

    Posted By: ELK1nG
    Rnaseq Data Analysis Using Shell Scripting And R

    Rnaseq Data Analysis Using Shell Scripting And R
    Published 5/2023
    MP4 | Video: h264, 1280x720 | Audio: AAC, 44.1 KHz
    Language: English | Size: 2.71 GB | Duration: 5h 16m

    Become a master in performing RNAseq analysis on linux command-line and use R to perform DE analysis and clustering

    What you'll learn

    Basics of NGS data analysis and how to perform Differential gene expression analysis for RNAseq dataset

    Generating Quality Control metrics and statistics

    Mapping Reads to the genome

    Differential gene expression

    Using Conda for installation of bioinformatics tools

    Processing RNA sequencing data

    UNIX command-line tools for processing the data

    Transcript quantification

    Performing Principal Component Analysis (PCA)

    Performing Clustering analysis using gene expression data

    Requirements

    Background knowledge of biology

    Interest in working with UNIX command-line tools

    Interest in bioinformatics tools installation

    Interest in genomics as well as applying computational methods for processing transcriptomics datasets

    No programming experience needed. You will learn everything you need to know

    All downloadable resources provided

    Description

    In this course, you will learn how to perform RNAseq data analysis via linux command line. This course provides a comprehensive introduction to RNAseq data analysis, covering the key concepts and tools needed to perform differential expression analysis and functional annotation of RNAseq data. Students will learn how to preprocess raw sequencing data, perform quality control, and align reads to a reference genome or transcriptome. The course will also cover differential expression analysis using statistical methods and visualisation of results using popular tools such as R. You will learn how to do end-to-end RNAseq data analysis which includes pre-processing of RNAseq data, Quality Control analysis, Differential Gene Expression analysis, Clustering and Principal Component Analysis of the gene expression data. You will also learn how to download data, install the bioinformatics/IT softwares using Conda/Anaconda on Mac, Windows or Linux platforms. I will guide you through performing differential expression analysis on RStudio (graphical user interface for R language).Throughout the course, students will work with real-world datasets and gain hands-on experience with popular bioinformatics tools and software packages. By the end of the course, students will have a thorough understanding of RNAseq data analysis and will be able to perform their own analyses of gene expression data. This course is ideal for researchers, scientists, and students who are interested in understanding the molecular basis of gene expression and exploring the potential applications of RNAseq technology. No prior bioinformatics or programming experience is required, but a basic knowledge of molecular biology and genetics is recommended.

    Overview

    Section 1: Introduction and Installation

    Lecture 1 Introduction

    Lecture 2 Installing Conda

    Lecture 3 Installing Bioinformatics tools using Conda

    Section 2: Preparing Data for Analysis

    Lecture 4 Organising the files

    Lecture 5 Obtaining the Raw Data

    Lecture 6 Obtaining the Genome files

    Section 3: Quality Control of RNA-seq data

    Lecture 7 QC analysis using FastQC for Single-End and Paired-End reads

    Section 4: Read Trimming and QC analysis

    Lecture 8 Adaptor and Quality Trimming using Trimmomatic

    Lecture 9 QC analysis of Trimmed Reads using MultiQC

    Section 5: Genome Indexing and Read Mapping

    Lecture 10 Genome Indexing using STAR

    Lecture 11 Read Mapping using STAR

    Section 6: Duplicate Read Marking

    Lecture 12 Marking Duplicate reads using Picard and indexing BAM files

    Section 7: Obtaining Alignment Statistics

    Lecture 13 Printing Alignment statistics using Bamtools

    Section 8: Obtaining Counts (read abundance) using FeatureCounts

    Lecture 14 Generating Gene Counts for DE analysis

    Section 9: Differential Expression (DE) analysis using DESeq2 on RStudio

    Lecture 15 Preparing the files for DE analysis

    Lecture 16 Installing libraries for DE analysis on RStudio

    Lecture 17 Performing the DE analysis using DESeq2 - Part1

    Lecture 18 Performing the DE analysis using DESeq2 - Part2

    Section 10: Principal Component Analysis and Clustering analysis of gene expression data

    Lecture 19 Performing PCA analysis and generating PCA plot

    Lecture 20 Performing Clustering analysis of gene expression data

    People interested in learning Next Generation Sequencing data analysis methods,Beginner Bioinformatician looking to understand end-to-end pipeline for transcriptomics data analysis,People looking to understand differential gene expression analysis,People interested to carry out bioinformatics analysis with command-line tools