Variant Calling using BCFTOOLS | BCFTOOLS Tutorial | Germline variant calling
This tutorial shows you how to call variants in sequence data using bcftools
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source of data
https://www.ncbi.nlm.nih.gov/pmc/arti...
sra-database
https://trace.ncbi.nlm.nih.gov/Traces...
Input Files
read 1
http://ftp.sra.ebi.ac.uk/vol1/run/ERR...
read 2
http://ftp.sra.ebi.ac.uk/vol1/run/ERR...
reference genome
https://www.ncbi.nlm.nih.gov/nuccore/...
accession id for reference genome
CP000325.1
Documentation of the tools
samtools
http://www.htslib.org/doc/samtools-fl...
bcftools
http://samtools.github.io/bcftools/bc...
https://samtools.github.io/bcftools/b...
bwa
http://bio-bwa.sourceforge.net/
sickle
https://github.com/najoshi/sickle
Setting up your PC
How to install Anaconda
Linux • Install , Configure and Run Anaconda ...
MacOS • Install, Configure and Run Anaconda i... - GUI Installer
• Install, Configure and Run Anaconda i... - Command line installer
How to install bcftools
Compile the source code: • How to install BCFTOOLS in any Linux ...
Using anaconda: • Install BCFTOOLS in Linux using anaco...
Chapters
00:10 intro
01:35 install tools using conda
05:22 download sequence reads using wget
09:30 download the reference genome using your browser
11:04 download the reference genome using python
15:29 trim the raw reads using sickle
21:03 index the reference genome using bwa index command
24:11 genome mapping using bwa
26:53 convert the sam file to bam file using samtools
28:46 sort the bam file using samtools
29:42 map and sort using a one liner command
32:21 get the mapping statistics using samtools
35:33 get the converage information for bases and calculate genotype likelyhoods
39:18 call variants using bcftools
41:08 post-vcf analysis using bcftools
#bioinformatics #genome #genomics #linuxforbeginners #genomesequencing
Commands used in this tutorial
bwa index
bwa mem
samtools view
samtools sort
samtools index
samtools flagstat
bcftools mpileup
bcftools call
bcftools view
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