phantompeakqualtools
phantompeakqualtools computes enrichment and quality metrics for ChIP-seq, DNase-seq, FAIRE-seq, and MNase-seq to assess predominant fragment lengths, characteristic tag shift values, and signal enrichment for genome-wide protein–DNA interaction assays.
Key Features:
- Quality Metrics Computation: Computes estimates of predominant fragment lengths and characteristic tag shift values and generates enrichment and quality measures for ChIP-seq, DNase-seq, FAIRE-seq, and MNase-seq.
- Systematic Quality Analysis: Performs uniform quality assessment across large datasets, including evaluation of vertebrate transcription factor ChIP-seq datasets from the Gene Expression Omnibus (GEO).
- Data Stratification: Assesses data quality at early experimental stages to stratify datasets by suitability for downstream analyses.
- Guidance for Experimental Design: Provides quality-derived metrics and insights that can guide experimental design and dataset inclusion decisions.
- Peak Calling and Data Interpretation: Identifies control datasets and enrichment-like background structures that may confound peak calling and lead to misinterpretation.
Scientific Applications:
- Transcription Factor Binding Studies: Supports mapping of transcription factor binding sites by selecting and validating high-quality ChIP-seq datasets.
- Histone Modification Mapping: Improves reliability of histone modification localization by filtering low-quality ChIP-seq datasets.
- Community-wide Data Integration: Enables identification and validation of high-quality datasets for large-scale integrated analyses across repositories such as GEO.
Methodology:
Computes enrichment and quality measures including fragment length and tag shift estimation, incorporates ENCODE project-derived metrics, detects protein-binding positions, improves tag alignment, corrects background signals, and evaluates the relationship between sequencing depth and binding site characteristics.
Topics
Details
- License:
- MIT
- Maturity:
- Mature
- Cost:
- Free of charge
- Tool Type:
- workflow
- Operating Systems:
- Linux
- Programming Languages:
- R, C++
- Added:
- 4/25/2019
- Last Updated:
- 11/24/2024
Operations
Publications
Marinov GK, Kundaje A, Park PJ, Wold BJ. Large-Scale Quality Analysis of Published ChIP-seq Data. G3 Genes|Genomes|Genetics. 2014;4(2):209-223. doi:10.1534/g3.113.008680. PMID:24347632. PMCID:PMC3931556.
Kharchenko PV, Tolstorukov MY, Park PJ. Design and analysis of ChIP-seq experiments for DNA-binding proteins. Nature Biotechnology. 2008;26(12):1351-1359. doi:10.1038/nbt.1508. PMID:19029915. PMCID:PMC2597701.
Landt SG, Marinov GK, Kundaje A, Kheradpour P, Pauli F, Batzoglou S, Bernstein BE, Bickel P, Brown JB, Cayting P, Chen Y, DeSalvo G, Epstein C, Fisher-Aylor KI, Euskirchen G, Gerstein M, Gertz J, Hartemink AJ, Hoffman MM, Iyer VR, Jung YL, Karmakar S, Kellis M, Kharchenko PV, Li Q, Liu T, Liu XS, Ma L, Milosavljevic A, Myers RM, Park PJ, Pazin MJ, Perry MD, Raha D, Reddy TE, Rozowsky J, Shoresh N, Sidow A, Slattery M, Stamatoyannopoulos JA, Tolstorukov MY, White KP, Xi S, Farnham PJ, Lieb JD, Wold BJ, Snyder M. ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia. Genome Research. 2012;22(9):1813-1831. doi:10.1101/gr.136184.111. PMID:22955991. PMCID:PMC3431496.