» Articles » PMID: 22936215

Identifying ChIP-seq Enrichment Using MACS

Overview
Journal Nat Protoc
Specialties Biology
Pathology
Science
Date 2012 Sep 1
PMID 22936215
Citations 955
Authors
Affiliations
Soon will be listed here.
Abstract

Model-based analysis of ChIP-seq (MACS) is a computational algorithm that identifies genome-wide locations of transcription/chromatin factor binding or histone modification from ChIP-seq data. MACS consists of four steps: removing redundant reads, adjusting read position, calculating peak enrichment and estimating the empirical false discovery rate (FDR). In this protocol, we provide a detailed demonstration of how to install MACS and how to use it to analyze three common types of ChIP-seq data sets with different characteristics: the sequence-specific transcription factor FoxA1, the histone modification mark H3K4me3 with sharp enrichment and the H3K36me3 mark with broad enrichment. We also explain how to interpret and visualize the results of MACS analyses. The algorithm requires ∼3 GB of RAM and 1.5 h of computing time to analyze a ChIP-seq data set containing 30 million reads, an estimate that increases with sequence coverage. MACS is open source and is available from http://liulab.dfci.harvard.edu/MACS/.

Citing Articles

IL-1 signaling enrichment in inflammatory skin disease loci with higher-risk allele frequencies in African ancestry.

Tsoi L, Dong Y, Patrick M, Sarkar M, Zhang H, Bogle R Res Sq. 2025; .

PMID: 39975900 PMC: 11838759. DOI: 10.21203/rs.3.rs-5724270/v1.


Histone Variant H2A.Z Cooperates with EBNA1 to Maintain Epstein-Barr Virus Latent Epigenome.

Castro-Munoz J, Maestri D, Yoon L, Karisetty B, Tempera I, Lieberman P bioRxiv. 2025; .

PMID: 39975074 PMC: 11838259. DOI: 10.1101/2025.01.28.635203.


An AT-hook transcription factor promotes transcription of histone, spliced-leader, and piRNA clusters.

Wang Y, Hertz H, Pastore B, Tang W Nucleic Acids Res. 2025; 53(4).

PMID: 39945323 PMC: 11822377. DOI: 10.1093/nar/gkaf079.


Simultaneous profiling of chromatin-associated RNA at targeted DNA loci and RNA-RNA Interactions through TaDRIM-seq.

Ding C, Chen G, Luan S, Gao R, Fan Y, Zhang Y Nat Commun. 2025; 16(1):1500.

PMID: 39929795 PMC: 11811046. DOI: 10.1038/s41467-024-53534-5.


CENP-A/CENP-B uncoupling in the evolutionary reshuffling of centromeres in equids.

Cappelletti E, Piras F, Biundo M, Raimondi E, Nergadze S, Giulotto E Genome Biol. 2025; 26(1):23.

PMID: 39915813 PMC: 11804003. DOI: 10.1186/s13059-025-03490-0.


References
1.
Liu E, Pott S, Huss M . Q&A: ChIP-seq technologies and the study of gene regulation. BMC Biol. 2010; 8:56. PMC: 2871264. DOI: 10.1186/1741-7007-8-56. View

2.
Li H, Durbin R . Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics. 2009; 25(14):1754-60. PMC: 2705234. DOI: 10.1093/bioinformatics/btp324. View

3.
Liu T, Ortiz J, Taing L, Meyer C, Lee B, Zhang Y . Cistrome: an integrative platform for transcriptional regulation studies. Genome Biol. 2011; 12(8):R83. PMC: 3245621. DOI: 10.1186/gb-2011-12-8-r83. View

4.
Mardis E . ChIP-seq: welcome to the new frontier. Nat Methods. 2007; 4(8):613-4. DOI: 10.1038/nmeth0807-613. View

5.
Noordermeer D, Leleu M, Splinter E, Rougemont J, de Laat W, Duboule D . The dynamic architecture of Hox gene clusters. Science. 2011; 334(6053):222-5. DOI: 10.1126/science.1207194. View