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Status |
Public on Jul 11, 2015 |
Title |
Base-resolution detection of N4-methylcytosine in genomic DNA using 4mC-TAB-seq |
Organisms |
synthetic construct; Caldicellulosiruptor acetigenus |
Experiment type |
Methylation profiling by high throughput sequencing
|
Summary |
N4-methylcytosine is a major DNA modification integral to restriction-modification (R-M) systems in bacterial genomes. Here we describe 4mC-Tet-Assisted Bisulfite-sequencing (4mC-TAB-seq), a method that accurately and rapidly reveals the genome-wide locations of N4-methylcytosines at single-base resolution. By coupling Tet-mediated oxidation with a modified sodium bisulfite conversion reaction, unmodified cytosines and 5-methylcytosines are read out as thymines, whereas N4-methylcytosines are read out as cytosines revealing their positions throughout the genome.
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Overall design |
4mC-TAB-seq
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Contributor(s) |
Schmitz RJ |
Citation(s) |
26184871 |
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Submission date |
Nov 17, 2014 |
Last update date |
May 15, 2019 |
Contact name |
Robert J Schmitz |
E-mail(s) |
[email protected]
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Organization name |
University of Georgia
|
Department |
Genetics
|
Street address |
B416 Davison Life Sciences
|
City |
Athens |
State/province |
GA |
ZIP/Postal code |
30602 |
Country |
USA |
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Platforms (2) |
GPL19423 |
Illumina NextSeq 500 (Caldicellulosiruptor kristjanssonii) |
GPL19424 |
Illumina NextSeq 500 (synthetic construct) |
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Samples (7)
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Relations |
BioProject |
PRJNA267586 |
SRA |
SRP049960 |