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The ENCyclopedia Of DNA Elements (ENCODE) Project aims to identifyall functional elements in the human genome sequence. The pilotphase of the Project is focused on a specified 30 megabases(1%) of the human genome sequence and is organized as an internationalconsortium of computational and laboratory-based scientistsworking to develop and apply high-throughput approaches fordetecting all sequence elements that confer biological function.The results of this pilot phase will guide future efforts toanalyze the entire human genome.
ENCODE Project Scientific Management: National Human GenomeResearch Institute (E. A. Feingold, P. J. Good, M. S. Guyer,S. Kamholz, L. Liefer, K. Wetterstrand, F. S. Collins).InitialENCODE Pilot Phase Participants: Affymetrix, Inc. (T. R. Gingeras,D. Kampa, E. A. Sekinger, J. Cheng, H. Hirsch, S. Ghosh, Z.Zhu, S. Patel, A. Piccolboni, A. Yang, H. Tammana, S. Bekiranov,P. Kapranov, R. Harrison, G. Church, K. Struhl); Ludwig Institutefor Cancer Research (B. Ren, T. H. Kim, L. O. Barrera, C. Qu,S. Van Calcar, R. Luna, C. K. Glass, M. G. Rosenfeld); MunicipalInstitute of Medical Research (R. Guigo, S. E. Antonarakis,E. Birney, M. Brent, L. Pachter, A. Reymond, E. T. Dermitzakis,C. Dewey, D. Keefe, F. Denoeud, J. Lagarde, J. Ashurst, T. Hubbard,J. J. Wesselink, R. Castelo, E. Eyras); Stanford University(R. M. Myers, A. Sidow, S. Batzoglou, N. D. Trinklein, S. J.Hartman, S. F. Aldred, E. Anton, D. I. Schroeder, S. S. Marticke,L.Nguyen, J.Schmutz, J.Grimwood, M.Dickson, G. M. Cooper, E.A. Stone, G. Asimenos, M. Brudno); University of Virginia (A.Dutta,N.Karnani, C.M.Taylor, H. K. Kim, G. Robins); University ofWashington (G. Stamatoyannopoulos, J. A. Stamatoyannopoulos,M. Dorschner, P. Sabo, M. Hawrylycz, R. Humbert, J. Wallace,M. Yu, P. A. Navas, M. McArthur, W. S. Noble); Wellcome TrustSanger Institute (I. Dunham, C. M. Koch, R.M.Andrews, G.K.Clelland,S.Wilcox, J.C.Fowler, K.D. James, P. Groth, O. M. Dovey, P.D. Ellis, V. L. Wraight, A. J. Mungall, P. Dhami, H. Fiegler,C. F. Langford, N. P. Carter, D. Vetrie); Yale University (M.Snyder, G. Euskirchen, A. E. Urban, U. Nagalakshmi, J. Rinn,G. Popescu, P. Bertone, S.Hartman, J. Rozowsky, O. Emanuelsson,T. Royce, S. Chung, M. Gerstein, Z. Lian, J. Lian, Y. Nakayama,S. Weissman, V.Stolc, W.Tongprasit, H.Sethi). Additional ENCODEPilot Phase Participants: British Columbia Cancer Agency GenomeSciences Centre (S. Jones, M. Marra, H. Shin, J. Schein); BroadInstitute (M. Clamp, K. Lindblad-Toh, J. Chang, D. B. Jaffe,M. Kamal, E. S. Lander, T. S. Mikkelsen, J. Vinson, M. C. Zody);Children's Hospital Oakland Research Institute (P.J.deJong,K.Osoegawa, M.Nefedov, B.Zhu); National Human Genome ResearchInstitute/Computational Genomics Unit (A. D. Baxevanis, T. G.Wolfsberg); National Human Genome Research Institute/MolecularGenetics Section (F. S. Collins, G. E. Crawford, J. Whittle,I. E. Holt, T. J. Vasicek, D. Zhou, S. Luo); NIH IntramuralSequencing Center/National Human Genome Research Institute (E.D. Green, G. G. Bouffard, E. H. Margulies, M. E. Portnoy, N.F. Hansen, P. J. Thomas, J. C. McDowell, B. Maskeri, A. C. Young,J. R. Idol, R. W. Blakesley); National Library of Medicine (G.Schuler); Pennsylvania State University (W. Miller, R. Hardison,L. Elnitski, P. Shah); The Institute for Genomic Research (S.L. Salzberg, M. Pertea, W. H. Majoros); University of California,Santa Cruz (D. Haussler, D. Thomas, K. R. Rosenbloom, H. Clawson,A. Siepel, W. J. Kent). ENCODE Technology Development PhaseParticipants: Boston University (Z. Weng, S. Jin, A. Halees,H. Burden, U. Karaoz, Y. Fu, Y. Yu, C. Ding, C. R. Cantor);Massachusetts General Hospital (R. E. Kingston, J. Dennis);NimbleGen Systems, Inc.(R.D.Green, M.A.Singer, T.A. Richmond,J.E.Norton, P.JFarnham, M.J.Oberley, D.R. Inman); NimbleGenSystems, Inc. (M. R. McCormick, H. Kim, C. L. Middle, M. C.Pirrung); University of California, San Diego (X. D. Fu, Y.S. Kwon, Z. Ye); University of Massachusetts Medical School(J. Dekker, T. M. Tabuchi, N. Gheldof, J. Dostie, S. C. Harvey).
To whom correspondence should be addressed. E-mail: elise_feingold{at}nih.gov
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The prediction of protein subcellular localization from sequence: a shortcut to functional genome annotation.
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Reciprocal Binding of PARP-1 and Histone H1 at Promoters Specifies Transcriptional Outcomes.
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Bioinformatics
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Transcriptome annotation using tandem SAGE tags.
E. Rivals, A. Boureux, M. Lejeune, F. Ottones, O. Pecharroman Perez, J. Tarhio, F. Pierrat, F. Ruffle, T. Commes, and J. Marti (2007)
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Signatures of Functional Constraint at Aye-aye Opsin Genes: The Potential of Adaptive Color Vision in a Nocturnal Primate.
G. H. Perry, R. D. Martin, and B. C. Verrelli (2007)
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Optimized design and assessment of whole genome tiling arrays.
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Genome-Wide Mapping of in Vivo Protein-DNA Interactions.
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ENCODE: More genomic empowerment.
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The landscape of histone modifications across 1% of the human genome in five human cell lines.
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Butyrate mediates decrease of histone acetylation centered on transcription start sites and down-regulation of associated genes.
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Integrated analysis of experimental data sets reveals many novel promoters in 1% of the human genome.
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Genome Res.
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The DART classification of unannotated transcription within the ENCODE regions: Associating transcription with known and novel loci.
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Prominent use of distal 5' transcription start sites and discovery of a large number of additional exons in ENCODE regions.
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Analyses of deep mammalian sequence alignments and constraint predictions for 1% of the human genome.
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The ENCODEdb portal: Simplified access to ENCODE Consortium data.
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Assessing the performance of different high-density tiling microarray strategies for mapping transcribed regions of the human genome.
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Genome Res.
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FAIRE (Formaldehyde-Assisted Isolation of Regulatory Elements) isolates active regulatory elements from human chromatin.
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Genome Res.
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Unsupervised segmentation of continuous genomic data.
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Bioinformatics
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Transcriptional Interferences in cis Natural Antisense Transcripts of Humans and Mice.
N. Osato, Y. Suzuki, K. Ikeo, and T. Gojobori (2007)
Genetics
176, 1299-1306
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GAPWM: a genetic algorithm method for optimizing a position weight matrix.
J. S. Song, K. Maghsoudi, W. Li, E. Fox, J. Quackenbush, and X. Shirley Liu (2007)
Bioinformatics
23, 966-971
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Assessing the need for sequence-based normalization in tiling microarray experiments.
T. E. Royce, J. S. Rozowsky, and M. B. Gerstein (2007)
Bioinformatics
23, 988-997
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Demographic Histories and Patterns of Linkage Disequilibrium in Chinese and Indian Rhesus Macaques.
R. D. Hernandez, M. J. Hubisz, D. A. Wheeler, D. G. Smith, B. Ferguson, J. Rogers, L. Nazareth, A. Indap, T. Bourquin, J. McPherson, et al. (2007)
Science
316, 240-243
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Extreme genomic variation in a natural population.
K. S. Small, M. Brudno, M. M. Hill, and A. Sidow (2007)
PNAS
104, 5698-5703
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The implications of alternative splicing in the ENCODE protein complement.
M. L. Tress, P. L. Martelli, A. Frankish, G. A. Reeves, J. J. Wesselink, C. Yeats, P. l. Olason, M. Albrecht, H. Hegyi, A. Giorgetti, et al. (2007)
PNAS
104, 5495-5500
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In vitro analysis of DNA-protein interactions by proximity ligation.
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PNAS
104, 3067-3072
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Massive amplification of rolling-circle transposons in the lineage of the bat Myotis lucifugus.
Improving gene annotation using peptide mass spectrometry.
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Genome Res.
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The UCSC genome browser database: update 2007.
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Ensembl 2007.
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GenomeTrafac: a whole genome resource for the detection of transcription factor binding site clusters associated with conventional and microRNA encoding genes conserved between mouse and human gene orthologs.
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Microinversions in mammalian evolution.
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PNAS
103, 19824-19829
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A supervised hidden markov model framework for efficiently segmenting tiling array data in transcriptional and chIP-chip experiments: systematically incorporating validated biological knowledge.
J. Du, J. S. Rozowsky, J. O. Korbel, Z. D. Zhang, T. E. Royce, M. H. Schultz, M. Snyder, and M. Gerstein (2006)
Bioinformatics
22, 3016-3024
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Locating mammalian transcription factor binding sites: A survey of computational and experimental techniques.
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Genome Res.
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Unraveling transcription regulatory networks by protein-DNA and protein-protein interaction mapping.
A computational genomics approach to identify cis-regulatory modules from chromatin immunoprecipitation microarray data--A case study using E2F1.
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Genome Res.
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Chromosome Conformation Capture Carbon Copy (5C): A massively parallel solution for mapping interactions between genomic elements.
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Genome Res.
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Mapping of the juxtacentromeric heterochromatin-euchromatin frontier of human chromosome 21.
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A genome-wide study of preferential amplification/hybridization in microarray-based pooled DNA experiments.