The materials in this repository are based on educational courses I have taken
It can be used as a helpful repository with cheat-sheets for NGS studies.
Typical workflow of NGS data analysis
To recreate any of the steps of this manual please install:
conda env create -f ngs-manual.yml
And of cource do not forget to activate the envinronment!
conda activate ngs-manual
- Reference-free approach in the comparative analysis of metagenomic data
- Whole Genome and Pangenome Analyses
- 16S Amplicon Analysis
In the Genomic Variation Analysis folder there is a detailed guide how to conduct studies on Variant Calling using fastqc
, trimmomatic
, bwa
, samtools
, abra2
, bcftools
, snpEff
& SnpSift
In the Quality Control folder there is a detailed guide how to conduct quality control of raw data using fastqc
and trimmomatic
.