Practical NGS Data Analysis for Variant Calling using Linux
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1:50:43
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1. Introduction to Variant Calling.mp4
05:28
2. Course Activities.mp4
03:38
3. Introduction to Variant Calling for Beginners.html
1. Introduction To Linux.mp4
18:40
2.1 Lecture+01.pdf
2. Bash Basic Commands.mp4
15:46
3.1 Bioinformatics+tools.pptx
3. Bioinformatics Tools Installation.mp4
09:09
4. Making WSL in Windows OS.mp4
05:06
1. Conda Setup and Channels Creation.mp4
07:50
2. Setting up the tools in WSL.mp4
03:47
3. Understanding workflow and metadata.mp4
03:19
1. Downloading Dataset.mp4
03:08
Files.zip
1. Quality Control of Paired Samples.mp4
08:23
Files.zip
1. Checking And Indexing the Genome.mp4
03:55
2. Mapping The Reads To Genome.mp4
04:18
3. Filtering The Mapped Reads.mp4
04:29
4. Marking the Duplicates Variants and Removing Them.mp4
01:36
Files.zip
1. Calling And Indexing Variants Files.mp4
06:53
2. Filtering The Variants.mp4
05:18
Files.zip
1. Final-Project Analyze any dataset from start to finish.html
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- language english
- Training sessions 17
- duration 1:50:43
- Release Date 2024/11/03
