Samtools

A toolkit for manipulating and analyzing high-throughput sequencing data in BAM and SAM formats.

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.

Key Features of Samtools

Wide Format Support: Efficiently handles SAM, BAM, and CRAM formats.
Data Processing Capabilities: Includes viewing, sorting, and indexing functionalities.
Genomic Analysis: Facilitates various analyses including variant calling and alignment.

Applications and Services

Genomic Research: Supports a range of genomic studies and analyses.
Bioinformatics Pipelines: Integrates into bioinformatics workflows for high-throughput sequencing data processing.

Resources and Learning Material

How to Run Samtools Analysis

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.

Steps to Execute on Our Platform

Upload Files: Click on the folder icon next to the Volume line and upload ex1.fa, ex1.sam.gz, and run_script.sh to the working directory of your project.
Set Project Directory: Make sure the Project Directory is set to /data (or the directory you've specified).
Configure Run Script: In the Run Script field, enter bash run_script.sh to specify the script for execution.
Create the Project: Click on Create to prepare your project with the necessary software and settings.
Run the Container: Navigate to the project tab and start the container to run the script.

Following these steps will initiate the Samtools analysis, providing valuable insights into the sequencing data quality.