- Level Foundation
- المدة 12 ساعات hours
- الطبع بواسطة Johns Hopkins University
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Offered by
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Introduces to the commands that you need to manage and analyze directories, files, and large sets of genomic data. This is the fourth course in the Genomic Big Data Science Specialization from Johns Hopkins University.الوحدات
Welcome to the course
5
Readings
- Welcome Message
- Syllabus
- VMBox Download & Instructions
- Docker Image Download & Instructions
- Pre-Course Survey
Basic Unix Commands
12
Videos
- Basic Unix Commands 1: Content Representation
- Basic Unix Commands 2: Files, Directories, Paths
- Basic Unix Commands 3: File Naming
- Basic Unix Commands 4: Content Creation
- Basic Unix Commands 5: Accessing Content I
- Basic Unix Commands 6: Accessing Content II
- Basic Unix Commands 7: Redirecting Content
- Basic Unix Commands 8: Querying Content
- Basic Unix Commands 9: Comparing Content
- Basic Unix Commands 10: Archiving Content
- Basic Unix Commands 11: Practical Exercises I
- Basic Unix Commands 12: Practical Exercises II
Quiz & Exam
2
Assignment
- Module 1 Quiz
- Module 1 Exam
1
Readings
- Module 1 Exam Instructions **IMPORTANT**
Module 2
11
Videos
- Sequences and Genomic Features 1: Molecular Bio Primer
- Sequences and Genomic Features 2: Sequence Representation and Generation
- Sequences and Genomic Features 3: Annotation
- Sequences and Genomic Features 4.1: Alignment I
- Sequences and Genomic Features 4.2: Alignment II
- Sequences and Genomic Features 5: Recreating Sequences & Features
- Sequences and Genomic Features 6: Genomic Feature Retrieval
- Sequences and Genomic Features 7: SAMtools I
- Sequences and Genomic Features 8: SAMtools II
- Sequences and Genomic Features 9: BEDtools I
- Sequences and Genomic Features 10: BEDtools II
Quiz & Exam
2
Assignment
- Module 2 Quiz
- Module 2 Exam
1
Readings
- Module 2 Exam Instructions **IMPORTANT**
Module 3
8
Videos
- Alignment & Sequence Variation 1: Overview
- Alignment & Sequence Variation 2: Alignment & Variant Detection Tools
- Alignment & Sequence Variation 3: VCF
- Alignment & Sequence Variation 4: Bowtie
- Alignment & Sequence Variation 5: BWA
- Alignment & Sequence Variation 6: SAMtools (mpileup)
- Alignment & Sequence Variation 7: BCFtools
- Alignment & Sequence Variation 8: Variant Calling
Quiz & Exam
2
Assignment
- Module 3 Quiz
- Module 3 Exam
1
Readings
- Module 3 Exam Instructions **IMPORTANT**
Module 4
8
Videos
- Tools for Transcriptomics 1: Overview
- Tools for Transcriptomics 2: RNA-seq
- Tools for Transcriptomics 3.1: Tophat I
- Tools for Transcriptomics 3.2: Tophat II
- Tools for Transcriptomics 4: Cufflinks
- Tools for Transcriptomics 5: Cuffdiff
- Tools for Transcriptomics 6.1: Integrated Genomics Viewer I
- Tools for Transcriptomics 6.2: Integrated Genomics Viewer II
Quiz & Exam
2
Assignment
- Module 4 Quiz
- Module 4 Exam
1
Readings
- Module 4 Exam Instructions **IMPORTANT**
Post-Course Survey
1
Readings
- Post-Course Survey
Auto Summary
Discover the essential tools for managing and analyzing genomic data with the "Command Line Tools for Genomic Data Science" course, part of Johns Hopkins University's Genomic Big Data Science Specialization on Coursera. This foundational course immerses you in the commands necessary for handling directories, files, and extensive genomic datasets, equipping you with practical skills for the data science and AI domain. Spanning 720 minutes of engaging content, the course is designed for beginners and is accessible through a Starter subscription. Ideal for those looking to build a robust foundation in genomic data analysis, this course is perfect for aspiring data scientists and genomic researchers eager to enhance their command line proficiency.

Liliana Florea, PhD