Bioinformatics ReviewBioinformatics Review
Notification Show More
Font ResizerAa
  •  Home
  • Docking
  • MD Simulation
  • Tools
  • More Topics
    • Softwares
    • Sequence Analysis
    • Algorithms
    • Bioinformatics Programming
    • Bioinformatics Research Updates
    • Drug Discovery
    • Phylogenetics
    • Structural Bioinformatics
    • Editorials
    • Tips & Tricks
    • Bioinformatics News
    • Featured
    • Genomics
    • Bioinformatics Infographics
  • Community
    • BiR-Research Group
    • Community Q&A
    • Ask a question
    • Join Telegram Channel
    • Join Facebook Group
    • Join Reddit Group
    • Subscription Options
    • Become a Patron
    • Write for us
  • About Us
    • About BiR
    • BiR Scope
    • The Team
    • Guidelines for Research Collaboration
    • Feedback
    • Contact Us
    • Recent @ BiR
  • Subscription
  • Account
    • Visit Dashboard
    • Login
Font ResizerAa
Bioinformatics ReviewBioinformatics Review
Search
Have an existing account? Sign In
Follow US
NGS

How to extract methylation call using Bismark?

Dr. Muniba Faiza
Last updated: April 20, 2021 6:43 pm
Dr. Muniba Faiza
Share
3 Min Read
How to extract methylation call using Bismark?
SHARE

Bismark is bioinformatics to map bisulfite treated sequencing reads and to perform methylation calls [1]. In this article, we are going to extract methylation information from Bismark alignment outputs.

Contents
1. Preparing genome (Indexing)2. Alignment3. Deduplication4. Methylation ExtractionReference

1. Preparing genome (Indexing)

Let’s first prepare our genome as it should be bisulfite converted to proceed further. This step needs to be done only once.

$ bismark_genome_preparation [options] /path/to/genome/folder

Let’s assume your genome is present in Documents/genomes/homo_sapiens/.

If Bowtie2 is not in your path, then use the following command for genome preparation:

$ bismark_genome_preparation --path_to_aligner /usr/bin/bowtie2/ --verbose /Documents/genomes/homo_sapiens/GRCh38/

2. Alignment

In this step, we perform the actual bisulfite alignment. Here, you have to specify the directory containing the genome of interest in FASTA format and a single or multiple sequence files to be analyzed. These files must be in FastA or FastQ format.

$ bismark [options] --genome <genome_folder> {-1 <mates1> -2 <mates2> | <singles>}

For example, let’s say your sequence file is test_data.fastq and is present in the same directory, then the command will be as shown below:

$ bismark --genome /Documents/genomes/homo_sapiens/GRCh37/ test_data.fastq

This will produce two files as output:

  • test_data_bismark_bt2.bam – This file will contain all alignments and methylation call strings.
  • test_data_bismark_SE_report.txt –  This file will contain alignment and methylation summary.

3. Deduplication

This step is performed to deduplicate the Bismark alignment BAM file. It will remove all reads except the one aligned to the very same position.

$ deduplicate_bismark --bam [options] <filenames>

4. Methylation Extraction

This command will extract the context-dependent (CpG/CHG/CHH) methylation. Here, we will use the output file generated in step 2.

$ bismark_methylation_extractor [options] <filenames>

For example,

$ bismark_methylation_extractor --gzip --bedGraph test_data_bismark_bt2.bam

This command will generate three main output files and two other files:

  • CpG_context_test_dataset_bismark_bt2.txt.gz
  • CHG_context_test_dataset_bismark_bt2.txt.gz
  • CHH_context_test_dataset_bismark_bt2.txt.gz
  • A bedgraph, and
  • Bismark coverage file

The output files will show:

  • seq-ID
  • methylation state
  • chromosome
  • start position (end position)
  • methylation call

For more information on output, click here.


Reference

  1. Krueger, F., & Andrews, S. R. (2011). Bismark: a flexible aligner and methylation caller for Bisulfite-Seq applications. bioinformatics, 27(11), 1571-1572.
TAGGED:BismarkgenomeMethylation extraction
Share This Article
Facebook Copy Link Print
ByDr. Muniba Faiza
Follow:
Dr. Muniba is a Bioinformatician based in New Delhi, India. She has completed her PhD in Bioinformatics from South China University of Technology, Guangzhou, China. She has cutting edge knowledge of bioinformatics tools, algorithms, and drug designing. When she is not reading she is found enjoying with the family. Know more about Muniba
Leave a Comment

Leave a Reply Cancel reply

You must be logged in to post a comment.

- Advertisement -
Ad image
10 years of Bioinformatics Review: From a Blog to a Bioinformatics Knowledge Hub!
Editorial
Starting in Bioinformatics? Do This First!
Starting in Bioinformatics? Do This First!
Tips & Tricks
[Editorial] Is it ethical to change the order of authors’ names in a manuscript?
Editorial Opinion
Installing bbtools on Ubuntu
[Tutorial] Installing BBTools on Ubuntu (Linux).
Sequence Analysis Software Tools

You Might Also Like

HTSNGSTranscriptomics

Assembly of high-throughput mRNA-Seq data: A review

June 12, 2020
How to generate config file for docking using Autodock Tools?
NGSNGS Data Analysis

[Tutorial] Trailing of paired end reads using Trimmomatic tool in GALAXY.

October 22, 2021
NGSSequence AnalysisSoftware

ALFALFA explained

December 11, 2015
Meta AnalysisNGSSequence AnalysisTools

Predictive metagenomics profiling: why, what and how ?

May 20, 2020
Copyright 2024 IQL Technologies
  • Journal
  • Customer Support
  • Contact Us
  • FAQs
  • Terms of Use
  • Privacy Policy
  • Cookie Policy
  • Sitemap
Welcome Back!

Sign in to your account

Username or Email Address
Password

Lost your password?

Not a member? Sign Up