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Status |
Public on Nov 15, 2010 |
Title |
Accurate inference of transcription factor binding from DNA sequence and chromatin accessibility data |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
|
Summary |
Accurate functional annotation of regulatory elements is essential for understanding global gene regulation. Here, we report a genome-wide map of 827,000 transcription factor binding sites in human lymphoblastoid cell lines, which is comprised of sites correspond-ing to 239 position weight matrices of known transcription factor binding motifs, and 49 novel sequence motifs. To generate this map, we developed a probabilistic framework that integrates cell- or tissue-specific experimental data such as histone modifications and DNa-seI cleavage patterns with genomic information such as gene annotation and evolutionary conservation. Comparison to empirical ChIP-seq data suggests that our method is highly accurate yet has the advantage of targeting many factors in a single assay. We anticipate that this approach will be a valuable tool for genome-wide studies of gene regulation in a wide variety of cell-types or tissues under diverse conditions.
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Overall design |
DNaseI-Seq on two YRI Hapmap cell lines. Each individual sequenced on 8 lanes of the Illumina Genome Analyzer II
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Contributor(s) |
Pique-Regi R, Degner JF, Pai AA, Gaffney D, Gilad Y, Pritchard JK |
Citation(s) |
21106904 |
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Submission date |
Nov 15, 2010 |
Last update date |
May 15, 2019 |
Contact name |
Jacob F Degner |
E-mail(s) |
[email protected]
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Organization name |
University of Chicago
|
Department |
Human Genetics
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Lab |
Pritchard
|
Street address |
920 E. 58th St
|
City |
Chicago |
State/province |
IL |
ZIP/Postal code |
60615 |
Country |
USA |
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Platforms (1) |
GPL9115 |
Illumina Genome Analyzer II (Homo sapiens) |
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Samples (16)
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Relations |
SRA |
SRP004446 |
BioProject |
PRJNA134875 |