A User's Guide to the Encyclopedia of DNA Elements (ENCODE)
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Raymond K. Auerbach | William Stafford Noble | Stephen C. J. Parker | Nathan C. Sheffield | Shane J. Neph | Juan M. Vaquerizas | Orion J. Buske | Kevin Y. Yip | David G. Knowles | Hugo Y. K. Lam | Christopher W. Maier | Morgan C. Giddings | Michael F. Lin | Maxwell W. Libbrecht | Alex P. Reynolds | Timothy E. Reddy | Barbara N. Pusey | Bernard B. Suh | Timothy J. Durham | Robert S. Harris | Robert C. Altshuler | D. Haussler | P. Bickel | T. Mikkelsen | D. Absher | E. Birney | S. Batzoglou | M. Gerstein | Z. Weng | G. Sherlock | A. Sidow | Hagen U. Tilgner | Fabian Grubert | J. Harrow | A. Frankish | M. Diekhans | F. Kokocinski | S. Searle | A. Bignell | V. Boychenko | T. Hunt | M. Kay | Gaurab Mukherjee | Gloria Despacio-Reyes | R. Harte | C. Howald | Andrea Tanzer | T. Derrien | J. Chrast | S. Balasubramanian | M. Tress | M. Brent | Manolis Kellis | A. Valencia | A. Reymond | R. Guigó | T. Hubbard | R. Sandstrom | J. Stamatoyannopoulos | W. J. Kent | T. Furey | K. Roskin | B. Williams | A. Mortazavi | B. Wold | Brian D. Reed | E. H. Margulies | W. Miller | V. Iyer | A. Kundaje | R. Myers | Paolo Ribeca | K. White | R. Grossman | K. Struhl | Z. Lu | P. Good | A. Brazma | N. Luscombe | A. Abyzov | Philip Cayting | M. Snyder | R. Kaul | E. Haugen | M. Weaver | Ekta Khurana | Jing Leng | L. Elnitski | K. Rosenbloom | E. Green | S. Weissman | P. Collins | I. Dunham | M. Sammeth | D. Winter | T. Gingeras | R. Thurman | P. Giresi | R. Humbert | Tristan Frum | P. Navas | P. Sabo | J. Dekker | J. Lieb | T. Tullius | G. Crawford | P. Kapranov | J. Rozowsky | Damian Keefe | Julien Lagarde | Atif Shahab | J. Drenkow | I. Bell | T. Alioto | C. Ucla | Jin Lian | P. Newburger | Piero Carninci | Y. Hayashizaki | Chia-Lin Wei | Y. Ruan | S. Antonarakis | E. Feingold | Haiyan Huang | B. Paten | R. Hardison | N. Trinklein | A. Bhinge | Z. Moqtaderi | Xiaoqin Xu | G. Euskirchen | P. Farnham | A. Zweig | G. Barber | R. Kuhn | D. Karolchik | S. Pepke | B. Bernstein | Theodore Gibson | A. Boyle | M. Cline | Kenneth McCue | A. Sboner | Tianyuan Wang | J. Ernst | B. Raney | O. Buske | J. Vaquerizas | G. Hannon | S. Djebali | A. Merkel | Xiaoan Ruan | T. Lassmann | N. Bhardwaj | Qunhua Li | Frank Doyle | Randall H. Brown | M. Mariotti | A. Dobin | Wei Lin | F. Schlesinger | G. Marinov | Jainab Khatun | C. Zaleski | Rehab F. Abdelhamid | P. Batut | K. Bell | S. Chakrabortty | Xian Chen | E. Dumais | Jacqueline Dumais | Hui Gao | Assaf Gordon | H. Gunawardena | Sonali Jha | Brandon King | C. Kingswood | Jonathan Preall | Brian A. Risk | Hazuki Takahashi | Diane Trout | Huaien Wang | Yanbao Yu | D. London | D. Raha | L. D. Ward | P. Kheradpour | Eric Rynes | Hao Wang | Kristen Lee | T. Kutyavin | Audra K. Johnson | T. Canfield | Erika Giste | Preti Jain | Kathryn Beal | Javier Herrero | A. Bansal | M. M. Hoffman | Koon-Kiu Yan | S. Landt | N. Shoresh | M. Hariharan | Chao Cheng | Alexandra E. Charos | S. Frietze | Jason Gertz | Maya Kasowski | P. Lacroute | Hannah Monahan | E. Partridge | Dorrelyn Patacsil | F. Pauli | Minyi Shi | T. Slifer | Jing Wang | Linfeng Wu | Xinqiong Yang | B. Lajoie | C. Epstein | Xiaolan Zhang | R. Issner | Michael J. Coyne | Manching Ku | Gilberto Desalvo | S. Karmakar | J. Vielmetter | V. Sotirova | L. Habegger | H. O'Geen | S. Wilder | D. Sobral | Lingyun Song | Li Wang | Ryan McDaniell | Jie Wang | Abigail K. Ebersol | Bum-Kyu Lee | D. Lotakis | Eric D Nguyen | Minerva E. Sanchez | A. Sanyal | Shinny Vong | Zhancheng Zhang | C. Davis | Xianjun Dong | T. Whitfield | H. Xi | R. Lowdon | Laura A. L. Dillon | S. Tenenbaum | Thanh Truong | C. A. Sloan | K. Learned | V. Malladi | T. Dreszer | L. Meyer | L. Grasfeder | Anna M. Battenhouse | Kimberly A. Showers | Christopher Shestak | Seul K.C. Kim | Zheng Liu | K. Varley | Henry Amrhein | K. Bowling | M. Muratet | K. Newberry | Amy S. Nesmith | S. Parker | Gary Saunders | M. V. Baren | Alina R. Cao | J. D. Fleming | S. Iyengar | Nathan Lamarre-Vincent | Marianne Lindahl-Allen | B. Miotto | L. O. Penalva | Alec Victorsen | M. Lukk | Nathan Boley | L. Lochovsky | L. Waite | R. Robilotto | Jiang Du | B. Rhead | Yoichiro Shibata | C. Borel | Katalin Toth Fejes | E. Graison | W. Poh | T. Vales | Rebekka O. Sprouse | Jason A. Dilocker | Krista S. Thibeault | K. Roberts | Anthony Kirilusha | Katherine Fisher | Rami Rauch | B. Aken | Youhan Xu | Kimberly R. Blahnik | Vaughan Roach | Jun Neri | Hadar H. Sheffer | Tony Shafer | Vanessa Swing | P. Fujita | James B. Brown | J. Jee | Giltae Song | S. Chittur | Nader Jameel | N. Bild | Ting Wang | Jonathan B. Preall | Kimberly M. Newberry | Kimberly M Newberry | J. Dumais | L. Penalva | Florencia Pauli | Sushma Iyengar | Tian-yuan Wang | B. Risk | M. Baren | H. O’Geen | A. Shahab | K. Fejes | Kevin Roberts | E. Margulies | Kathryn M Beal | C. Sloan | K. McCue | Amartya Sanyal | Katalin Fejes | F. Doyle | W. Kent | Jacqueline Chrast | Colin Kingswood | A. Tanzer | Carrie A. Davis | B. Rhead | Veronika Boychenko | Emilie Aït Yahya Graison | Robbyn Issner | Kevin Y. Yip
[1] E. Jaffe,et al. Culture of human endothelial cells derived from umbilical veins. Identification by morphologic and immunologic criteria. , 1973, The Journal of clinical investigation.
[2] C. Lozzio,et al. Human chronic myelogenous leukemia cell-line with positive Philadelphia chromosome. , 1975, Blood.
[3] C. Lozzio,et al. Human chronic myelogenous leukemia cell-line with positive Philadelphia chromosome. , 1975, Blood.
[4] D. Galas,et al. DNAse footprinting: a simple method for the detection of protein-DNA binding specificity. , 1978, Nucleic acids research.
[5] Carl Wu. The 5′ ends of Drosophila heat shock genes in chromatin are hypersensitive to DNase I , 1980, Nature.
[6] C C Howe,et al. Human hepatocellular carcinoma cell lines secrete the major plasma proteins and hepatitis B surface antigen. , 1980, Science.
[7] J. D. Engel,et al. A 200 base pair region at the 5′ end of the chicken adult β-globin gene is accessible to nuclease digestion , 1981, Cell.
[8] S. Elgin,et al. DNase I hypersensitive sites in Drosophila chromatin occur at the 5' ends of regions of transcription. , 1981, Proceedings of the National Academy of Sciences of the United States of America.
[9] D. S. Gross,et al. Nuclease hypersensitive sites in chromatin. , 1988, Annual review of biochemistry.
[10] G. Sermonti. The human genome. , 1988, Rivista di biologia.
[11] M. Frohman,et al. Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[12] J Cairns,et al. Cold spring harbor. , 1991, Science.
[13] S. Orkin,et al. In vivo protein-DNA interactions at hypersensitive site 3 of the human beta-globin locus control region. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[14] AC Tose. Cell , 1993, Cell.
[15] V. Rotter,et al. A novel transcript encoded within the 10-kb first intron of the human p53 tumor suppressor gene (D17S2179E) is induced during differentiation of myeloid leukemia cells. , 1996, Genomics.
[16] R. Jaenisch. DNA methylation and imprinting: why bother? , 1997, Trends in genetics : TIG.
[17] J. Thomson,et al. Embryonic stem cell lines derived from human blastocysts. , 1998, Science.
[18] C. Allis,et al. The language of covalent histone modifications , 2000, Nature.
[19] S. Tenenbaum,et al. Identifying mRNA subsets in messenger ribonucleoprotein complexes by using cDNA arrays. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[20] J. Dekker,et al. Capturing Chromosome Conformation , 2002, Science.
[21] Mouse Genome Sequencing Consortium. Initial sequencing and comparative analysis of the mouse genome , 2002, Nature.
[22] Barry Moore,et al. Genome-based peptide fingerprint scanning , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[23] A. Hüttenhofer,et al. The expanding snoRNA world. , 2002, Biochimie.
[24] Colin N. Dewey,et al. Initial sequencing and comparative analysis of the mouse genome. , 2002 .
[25] A. Bird. DNA methylation patterns and epigenetic memory. , 2002, Genes & development.
[26] S. Tenenbaum,et al. Ribonomics: identifying mRNA subsets in mRNP complexes using antibodies to RNA-binding proteins and genomic arrays. , 2002, Methods.
[27] F. Collins,et al. A vision for the future of genomics research , 2003, Nature.
[28] D Haussler,et al. The share of human genomic DNA under selection estimated from human-mouse genomic alignments. , 2003, Cold Spring Harbor symposia on quantitative biology.
[29] J. Kawai,et al. Cap analysis gene expression for high-throughput analysis of transcriptional starting point and identification of promoter usage , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[30] Peter A. Jones,et al. Distinct localization of histone H3 acetylation and H3-K4 methylation to the transcription start sites in the human genome. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[31] Tony Kouzarides,et al. Histone H3 lysine 4 methylation patterns in higher eukaryotic genes , 2004, Nature Cell Biology.
[32] Paul T. Groth,et al. The ENCODE (ENCyclopedia Of DNA Elements) Project , 2004, Science.
[33] J. Bonfield,et al. Finishing the euchromatic sequence of the human genome , 2004, Nature.
[34] J. Stamatoyannopoulos,et al. Discovery of functional noncoding elements by digital analysis of chromatin structure. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[35] S. Cawley,et al. Novel RNAs identified from an in-depth analysis of the transcriptome of human chromosomes 21 and 22. , 2004, Genome research.
[36] N. Nomura,et al. Complete sequencing and characterization of 21,243 full-length human cDNAs , 2004, Nature Genetics.
[37] International Human Genome Sequencing Consortium. Finishing the euchromatic sequence of the human genome , 2004 .
[38] Eric S. Lander,et al. Genomic Maps and Comparative Analysis of Histone Modifications in Human and Mouse , 2005, Cell.
[39] 宁北芳,et al. 疟原虫var基因转换速率变化导致抗原变异[英]/Paul H, Robert P, Christodoulou Z, et al//Proc Natl Acad Sci U S A , 2005 .
[40] S. Batzoglou,et al. Distribution and intensity of constraint in mammalian genomic sequence. , 2005, Genome research.
[41] Arend Sidow,et al. Trade-offs in detecting evolutionarily constrained sequence by comparative genomics. , 2005, Annual review of genomics and human genetics.
[42] James A. Cuff,et al. A Bivalent Chromatin Structure Marks Key Developmental Genes in Embryonic Stem Cells , 2006, Cell.
[43] Mark Gerstein,et al. PseudoPipe: an automated pseudogene identification pipeline , 2006, Bioinform..
[44] C. Nusbaum,et al. Chromosome Conformation Capture Carbon Copy (5C): a massively parallel solution for mapping interactions between genomic elements. , 2006, Genome research.
[45] D. Conrad,et al. Global variation in copy number in the human genome , 2006, Nature.
[46] Michael R. Green,et al. Transcriptional regulatory elements in the human genome. , 2006, Annual review of genomics and human genetics.
[47] J. Harrow,et al. GENCODE: producing a reference annotation for ENCODE , 2006, Genome Biology.
[48] Martin S. Taylor,et al. Genome-wide analysis of mammalian promoter architecture and evolution , 2006, Nature Genetics.
[49] Jordan M. Komisarow,et al. RIP-Chip: the isolation and identification of mRNAs, microRNAs and protein components of ribonucleoprotein complexes from cell extracts , 2006, Nature Protocols.
[50] William Stafford Noble,et al. Genome-scale mapping of DNase I sensitivity in vivo using tiling DNA microarrays , 2006, Nature Methods.
[51] Megan F. Cole,et al. Control of Developmental Regulators by Polycomb in Human Embryonic Stem Cells , 2006, Cell.
[52] J. Zeitlinger,et al. Polycomb complexes repress developmental regulators in murine embryonic stem cells , 2006, Nature.
[53] E. Birney,et al. EGASP: the human ENCODE Genome Annotation Assessment Project , 2006, Genome Biology.
[54] S. Nelson,et al. The problem of neuronal cell types: a physiological genomics approach , 2006, Trends in Neurosciences.
[55] Alexander Eckehart Urban,et al. in the human genome Systematic prediction and validation of breakpoints associated with copy-number variants , 2007 .
[56] T. Kouzarides. Chromatin Modifications and Their Function , 2007, Cell.
[57] T. Mikkelsen,et al. Genome-wide maps of chromatin state in pluripotent and lineage-committed cells , 2007, Nature.
[58] E. Lander,et al. The Mammalian Epigenome , 2007, Cell.
[59] Zhiping Weng,et al. Integrated analysis of experimental data sets reveals many novel promoters in 1% of the human genome. , 2007, Genome research.
[60] V. Iyer,et al. FAIRE (Formaldehyde-Assisted Isolation of Regulatory Elements) isolates active regulatory elements from human chromatin. , 2007, Genome research.
[61] William Stafford Noble,et al. Widely distributed noncoding purifying selection in the human genome , 2007, Proceedings of the National Academy of Sciences.
[62] Michael Q. Zhang,et al. Analysis of the Vertebrate Insulator Protein CTCF-Binding Sites in the Human Genome , 2007, Cell.
[63] Mikhail A. Roytberg,et al. Analysis of Sequence Conservation at Nucleotide Resolution , 2007, PLoS Comput. Biol..
[64] William Stafford Noble,et al. Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project , 2007, Nature.
[65] Zhiping Weng,et al. Transcription factor binding and modified histones in human bidirectional promoters. , 2007, Genome research.
[66] Allen D. Delaney,et al. Genome-wide profiles of STAT1 DNA association using chromatin immunoprecipitation and massively parallel sequencing , 2007, Nature Methods.
[67] R. Myers,et al. The ets-Related Transcription Factor GABP Directs Bidirectional Transcription , 2007, PLoS genetics.
[68] T. Gingeras,et al. Genome-wide transcription and the implications for genomic organization , 2007, Nature Reviews Genetics.
[69] Dustin E. Schones,et al. High-Resolution Profiling of Histone Methylations in the Human Genome , 2007, Cell.
[70] A. Mortazavi,et al. Genome-Wide Mapping of in Vivo Protein-DNA Interactions , 2007, Science.
[71] Nathaniel D. Heintzman,et al. Distinct and predictive chromatin signatures of transcriptional promoters and enhancers in the human genome , 2007, Nature Genetics.
[72] David Haussler,et al. The UCSC genome browser database: update 2007 , 2006, Nucleic Acids Res..
[73] Morgan C. Giddings,et al. Incorporating sequence information into the scoring function: a hidden Markov model for improved peptide identification , 2008, Bioinform..
[74] A. Jakubowska,et al. A range of cancers is associated with the rs6983267 marker on chromosome 8. , 2008, Cancer research.
[75] Karl Mechtler,et al. BAC TransgeneOmics: a high-throughput method for exploration of protein function in mammals , 2008, Nature Methods.
[76] S. Tenenbaum,et al. Advances in RIP-chip analysis : RNA-binding protein immunoprecipitation-microarray profiling. , 2008, Methods in molecular biology.
[77] B. Wold,et al. Sequence census methods for functional genomics , 2008, Nature Methods.
[78] T. Mikkelsen,et al. Genome-scale DNA methylation maps of pluripotent and differentiated cells , 2008, Nature.
[79] E. Birney,et al. Enredo and Pecan: genome-wide mammalian consistency-based multiple alignment with paralogs. , 2008, Genome research.
[80] Z. Weng,et al. High-Resolution Mapping and Characterization of Open Chromatin across the Genome , 2008, Cell.
[81] Job Dekker,et al. Long-range chromosomal interactions and gene regulation. , 2008, Molecular bioSystems.
[82] Michael J MacCoss,et al. Use of shotgun proteomics for the identification, confirmation, and correction of C. elegans gene annotations. , 2008, Genome research.
[83] E. Birney,et al. Genome-wide nucleotide-level mammalian ancestor reconstruction. , 2008, Genome research.
[84] Christopher M. Vockley,et al. Detection and characterization of silencers and enhancer-blockers in the greater CFTR locus. , 2008, Genome research.
[85] B. Williams,et al. Mapping and quantifying mammalian transcriptomes by RNA-Seq , 2008, Nature Methods.
[86] Judy H. Cho,et al. Finding the missing heritability of complex diseases , 2009, Nature.
[87] Timothy E. Reddy,et al. Distinct DNA methylation patterns characterize differentiated human embryonic stem cells and developing human fetal liver. , 2009, Genome research.
[88] P. Giresi,et al. Isolation of active regulatory elements from eukaryotic chromatin using FAIRE (Formaldehyde Assisted Isolation of Regulatory Elements). , 2009, Methods.
[89] Christopher P Austin,et al. Prepublication data sharing , 2009, Nature.
[90] K. White,et al. Genomic Antagonism between Retinoic Acid and Estrogen Signaling in Breast Cancer , 2009, Cell.
[91] N. Camp,et al. Meta Association of Colorectal Cancer Confirms Risk Alleles at 8q24 and 18q21 , 2009, Cancer Epidemiology Biomarkers & Prevention.
[92] D. Price,et al. Formaldehyde‐assisted isolation of regulatory elements , 2009, Wiley interdisciplinary reviews. Systems biology and medicine.
[93] R. Sandstrom,et al. CCCTC-binding factor and the transcription factor T-bet orchestrate T helper 1 cell-specific structure and function at the interferon-gamma locus. , 2009, Immunity.
[94] D. Reich,et al. Functional Enhancers at the Gene-Poor 8q24 Cancer-Linked Locus , 2009, PLoS genetics.
[95] Ali Amin Al Olama,et al. Multiple loci on 8q24 associated with prostate cancer susceptibility , 2009, Nature Genetics.
[96] klaguia. Prepublication Data Sharing , 2009 .
[97] Jun Kawai,et al. Genome-wide detection and analysis of hippocampus core promoters using DeepCAGE. , 2009, Genome research.
[98] Raymond K. Auerbach,et al. PeakSeq enables systematic scoring of ChIP-seq experiments relative to controls , 2009, Nature Biotechnology.
[99] Job Dekker,et al. My5C: web tools for chromosome conformation capture studies , 2009, Nature Methods.
[100] William Stafford Noble,et al. Global mapping of protein-DNA interactions in vivo by digital genomic footprinting , 2009, Nature Methods.
[101] M. Gerstein,et al. RNA-Seq: a revolutionary tool for transcriptomics , 2009, Nature Reviews Genetics.
[102] Esko Ukkonen,et al. The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling , 2009, Nature Genetics.
[103] F. Collins,et al. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits , 2009, Proceedings of the National Academy of Sciences.
[104] Stephen C. J. Parker,et al. Local DNA Topography Correlates with Functional Noncoding Regions of the Human Genome , 2009, Science.
[105] E. Liu,et al. Next-generation DNA sequencing of paired-end tags (PET) for transcriptome and genome analyses. , 2009, Genome research.
[106] Raymond K. Auerbach,et al. Mapping accessible chromatin regions using Sono-Seq , 2009, Proceedings of the National Academy of Sciences.
[107] Juan M. Vaquerizas,et al. A census of human transcription factors: function, expression and evolution , 2009, Nature Reviews Genetics.
[108] T. Jensen,et al. Nuclear quality control of RNA polymerase II transcripts , 2010, Wiley interdisciplinary reviews. RNA.
[109] E. Birney,et al. Heritable Individual-Specific and Allele-Specific Chromatin Signatures in Humans , 2010, Science.
[110] Z. Weng,et al. Sequence features that drive human promoter function and tissue specificity. , 2010, Genome research.
[111] Michael D. Cole,et al. Upregulation of c-MYC in cis through a Large Chromatin Loop Linked to a Cancer Risk-Associated Single-Nucleotide Polymorphism in Colorectal Cancer Cells , 2010, Molecular and Cellular Biology.
[112] K. Pollard,et al. Detection of nonneutral substitution rates on mammalian phylogenies. , 2010, Genome research.
[113] E. Eichler,et al. Characterization of Missing Human Genome Sequences and Copy-number Polymorphic Insertions , 2010, Nature Methods.
[114] Benjamin P. Blackburne,et al. Mutation spectrum revealed by breakpoint sequencing of human germline CNVs , 2010, Nature Genetics.
[115] Wolfgang Wagner,et al. Age-dependent DNA methylation of genes that are suppressed in stem cells is a hallmark of cancer. , 2010, Genome research.
[116] Chia-Lin Wei,et al. Dynamic changes in the human methylome during differentiation. , 2010, Genome research.
[117] R. Wilson,et al. Identification of a CpG island methylator phenotype that defines a distinct subgroup of glioma. , 2010, Cancer cell.
[118] Paul Mitchell,et al. Common Genetic Variants near the Brittle Cornea Syndrome Locus ZNF469 Influence the Blinding Disease Risk Factor Central Corneal Thickness , 2010, PLoS genetics.
[119] Gautier Koscielny,et al. Ensembl’s 10th year , 2009, Nucleic Acids Res..
[120] M. Snyder,et al. ChIP‐Seq: A Method for Global Identification of Regulatory Elements in the Genome , 2010, Current protocols in molecular biology.
[121] Ting Wang,et al. ENCODE whole-genome data in the UCSC Genome Browser , 2009, Nucleic Acids Res..
[122] Karen L. Mohlke,et al. A map of open chromatin in human pancreatic islets , 2010, Nature Genetics.
[123] M. Gerstein,et al. Dynamic transcriptomes during neural differentiation of human embryonic stem cells revealed by short, long, and paired-end sequencing , 2010, Proceedings of the National Academy of Sciences.
[124] Owen T McCann,et al. Human aging-associated DNA hypermethylation occurs preferentially at bivalent chromatin domains. , 2010, Genome research.
[125] M. Gerstein,et al. Variation in Transcription Factor Binding Among Humans , 2010, Science.
[126] David Haussler,et al. The UCSC Genome Browser database: update 2010 , 2009, Nucleic Acids Res..
[127] Mary Goldman,et al. The UCSC Genome Browser database: update 2011 , 2010, Nucleic Acids Res..
[128] Jacob F. Degner,et al. Sequence and Chromatin Accessibility Data Accurate Inference of Transcription Factor Binding from Dna Material Supplemental Open Access , 2022 .
[129] E. Birney,et al. High-resolution genome-wide in vivo footprinting of diverse transcription factors in human cells. , 2011, Genome research.