Samtools is a versatile suite of tools for processing and analyzing genomic data, particularly optimized for high-throughput sequencing data in SAM, BAM, and CRAM formats. It is widely used in genomics for tasks like viewing, sorting, and indexing genomic sequences.
Samtools is essential for:
Docker hub: Docker hub
Github: Github repository
This example demonstrates how to perform a Samtools analysis on sequencing data files. To execute the example, you'll need the reference FASTA file ex1.fa
, the compressed SAM file ex1.sam.gz
, and the script run_script.sh
.
You can download the necessary files through these links:
Volume
line and upload ex1.fa
, ex1.sam.gz
, and run_script.sh
to the working directory of your project.Project Directory
is set to /data
(or the directory you've specified).Run Script
field, enter bash run_script.sh
to specify the script for execution.Create
to prepare your project with the necessary software and settings.Following these steps will initiate the Samtools analysis, providing valuable insights into the sequencing data quality.
Sequencing Data Analysis
Quality Control
Bioinformatics
NGS
Data Quality Assessment