The UCSC Genome Browser Database: update 2006
Open accessAbstract
The University of California Santa Cruz Genome Browser Database (GBD) contains sequence and annotation data for the genomes of about a dozen vertebrate species and several major model organisms. Genome annotations typically include assembly data, sequence composition, genes and gene predictions, mRNA and expressed sequence tag evidence, comparative genomics, regulation, expression and variation data. The database is optimized to support fast interactive performance with web tools that provide powerful visualization and querying capabilities for mining the data. The Genome Browser displays a wide variety of annotations at all scales from single nucleotide level up to a full chromosome. The Table Browser provides direct access to the database tables and sequence data, enabling complex queries on genome-wide datasets. The Proteome Browser graphically displays protein properties. The Gene Sorter allows filtering and comparison of genes by several metrics including expression data and several gene properties. BLAT and In Silico PCR search for sequences in entire genomes in seconds. These tools are highly integrated and provide many hyperlinks to other databases and websites. The GBD, browsing tools, downloadable data files and links to documentation and other information can be found at http://genome.ucsc.edu/.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Chromosome 21 is one of five human acrocentric chromosomes (13, 14, 15, 21, and 22) that exhibit high sequence conservation and are characterized by an abundance of repetitive elements within their short arms.
“Chromosome 21 is one of five human acrocentric chromosomes (13, 14, 15, 21, and 22) that exhibit high sequence conservation and are characterized by an abundance of repetitive elements within their short arms (99, 100).”
From Molecular and cellular processes disrupted in the early postnatal Down syndrome prefrontal cortex (2026) · cites this paper as [99]
Our copy’s Chromosome ideogram section describes a display feature, and its Conservation section describes multi-species alignment scores; neither addresses acrocentric chromosomes. Searches for chromosomes 13, 14, 15, 21, and 22 and for repetitive elements in their short arms found no passage supporting the claim. The supplied passages have no page numbers. (LLM, conf=0.75)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Basic local alignment search tool
Altschul, S. F., Gish, W., Miller, W., Myers, E. W., & Lipman, D. J. (1990) · Journal of Molecular Biology · doi:10.1006/jmbi.1990.9999 · Cited by 98,669 · see citing works
Gene Ontology: tool for the unification of biology
Ashburner, M., Ball, C. A., Blake, J. A., Botstein, D., Butler, H., Cherry, J. M., Davis, A. P., Dolinski, K., Dwight, S. S., Eppig, J. T., et al. (2000) · Nature Genetics · doi:10.1038/75556 · Cited by 43,206 · see citing works
The Human Genome Browser at UCSC
Kent, W. J., Sugnet, C. W., Furey, T. S., Roskin, K. M., Pringle, T. H., Zahler, A. M., & Haussler, A. D. (2002) · Genome Research · doi:10.1101/gr.229102 · Cited by 10,400 · see citing works
Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes
Siepel, A., Bejerano, G., Pedersen, J. S., Hinrichs, A. S., Hou, M., Rosenbloom, K., Clawson, H., Spieth, J., Hillier, L. W., Richards, S., et al. (2005) · Genome Research · doi:10.1101/gr.3715005 · Cited by 4,408 · see citing works
Self-citation
Flagged first, then by citations
Research works printed but not linked: 49
- [1]Karolchik D. Baertsch R. Diekhans M. Furey T.S. Hinrichs A. Lu Y.T. Roskin K.M. Schwartz M. Sugnet C.W. Thomas D.J. The UCSC Genome Browser Database Nucleic Acids Res. 2003 31 51 54 12519945 PMC165576
- [2]Hsu F. Pringle T.H. Kuhn R.M. Karolchik D. Diekhans M. Haussler D. Kent W.J. The UCSC Proteome Browser Nucleic Acids Res. 2005 33 D454 D458 15608236 PMC540054
- [3]Karolchik D. Hinrichs A.S. Furey T.S. Roskin K.M. Sugnet C.W. Haussler D. Kent W.J. The UCSC Table Browser data retrieval tool Nucleic Acids Res. 2004 32 D493 D496 14681465 PMC308837
- [5]Schwartz S. Kent W.J. Smit A. Zhang Z. Baertsch R. Hardison R.C. Haussler D. Miller W. Human-mouse alignments with BLASTZ Genome Res. 2003 13 103 107 12529312 PMC430961
- [6]Kent W.J. Baertsch R. Hinrichs A. Miller W. Haussler D. Evolution's cauldron: duplication, deletion, and rearrangement in the mouse and human genomes Proc. Natl Acad. Sci. USA 2003 100 11484 11489 14500911 PMC208784
- [7]Blanchette M. Kent W.J. Riemer C. Elnitski L. Smit A.F.A. Roskin K.M. Baertsch R. Rosenbloom K. Clawson H. Green E.D. Aligning multiple genomic sequences with the threaded blockset aligner Genome Res. 2004 14 708 715 15060014 PMC383317
- [9]Bejerano G. Siepel A.C. Kent W.J. Haussler D. Computational screening of conserved genomic DNA in search of functional noncoding elements Nature Methods 2005 2 535 545 16170870
- [10]Bairoch A. Apweiler R. Wu C.H. Barker W.C. Boeckmann B. Ferro S. Gasteiger E. Huang H. Lopez R. Magrane M. The Universal Protein Resource (UniProt) Nucleic Acids Res. 2005 33 D154 D159 15608167 PMC540024
- [11]Benson D.A. Karsch-Mizrachi I. Lipman D.J. Ostell J. Wheeler D.L. GenBank Nucleic Acids Res. 2005 33 D34 D38 15608212 PMC540017
- [12]Kent W.J. Hsu F. Karolchik D. Kuhn R.M. Clawson H. Trumbower H. Haussler D. Exploring relationships and mining data with the UCSC Gene Sorter Genome Res. 2005 15 737 741 15867434 PMC1088302
- [13]Pruitt K.D. Tatusova T. Maglott D.R. NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins Nucleic Acids Res. 2005 33 D501 D504 15608248 PMC539979
- [14]Gerhard D.S. Wagner L. Feingold E.A. Shenmen C.M. Grouse L.H. Schuler G. Klein S.L. Old S. Rasooly R. Good P. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC) Genome Res. 2004 14 2121 2127 15489334 PMC528928
- [15]Mulder N.J. Apweiler R. Attwood T.K. Bairoch A. Bateman A. Binns D. Bradley P. Bork P. Bucher P. Cerutti L. InterPro, progress and status in 2005 Nucleic Acids Res. 2005 33 D201 D205 15608177 PMC540060
- [16]Bateman A. Coin L. Durbin R. Finn R.D. Hollich V. Griffiths-Jones S. Khanna A. Marshall M. Moxon S. Sonnhammer E.L. The Pfam protein families database Nucleic Acids Res. 2004 32 D138 D141 14681378 PMC308855
- [17]Deshpande N. Addess K.J. Bluhm W.F. Merino-Ott J.C. Townsend-Merino W. Zhang Q. Knezevich C. Xie L. Chen L. Feng Z. The RCSB Protein Data Bank: a redesigned query system and relational database based on the mmCIF schema Nucleic Acids Res. 2005 33 D233 D237 15608185 PMC540011
- [18]Pieper U. Eswar N. Braberg H. Madhusudhan M.S. Davis F.P. Stuart A.C. Mirkovic N. Rossi A. Marti-Renom M.A. Fiser A. MODBASE, a database of annotated comparative protein structure models, and associated resources Nucleic Acids Res. 2004 32 D217 D222 14681398 PMC308829
- [20]Camon E. Magrane M. Barrell D. Lee V. Dimmer E. Maslen J. Binns D. Harte N. Lopez R. Apweiler R. The Gene Ontology Annotation (GOA) Database: sharing knowledge in Uniprot with Gene Ontology Nucleic Acids Res. 2004 32 D262 D266 14681408 PMC308756
- [21]Kanehisa M. Goto S. Kawashima S. Okuno Y. Hattori M. The KEGG resource for deciphering the genome Nucleic Acids Res. 2004 32 D277 D280 14681412 PMC308797
- [22]Krummenacker M. Paley S. Mueller L. Yan T. Karp P.D. Querying and computing with BioCyc databases Bioinformatics 2005 21 3454 3455 15961440 PMC1450015
- [23]Joshi-Tope G. Gillespie M. Vastrik I. D'Eustachio P. Schmidt E. de Bono B. Jassal B. Gopinath G.R. Wu G.R. Matthews L. Reactome: a knowledgebase of biological pathways Nucleic Acids Res. 2005 33 D428 D432 15608231 PMC540026
- [24]Kent W.J. BLAT—the BLAST-like alignment tool Genome Res. 2002 12 656 664 11932250 PMC187518
- [26]Encode Project Consortium The ENCODE (ENCyclopedia Of DNA Elements) Project Science 2004 306 636 640 15499007
- [27]Hubbard T. Andrews D. Caccamo M. Cameron G. Chen Y. Clamp M. Clarke L. Coates G. Cox T. Cunningham F. Ensembl 2005 Nucleic Acids Res. 2005 33 D447 D453 15608235 PMC540092
- [28]Ashurst J.L. Chen C.K. Gilbert J.G. Jekosch K. Keenan S. Meidl P. Searle S.M. Stalker J. Storey R. Trevanion S. The Vertebrate Genome Annotation (Vega) database Nucleic Acids Res. 2005 33 D459 D465 15608237 PMC540089
- [29]Kim N. Shin S. Lee S. ECgene: genome-based EST clustering and gene modeling for alternative splicing Genome Res. 2005 15 566 576 15805497 PMC1074371
- [30]Flicek P. Keibler E. Hu P. Korf I. Brent M.R. Leveraging the mouse genome for gene prediction in human: from whole-genome shotgun reads to a global synteny map Genome Res. 2003 13 46 54 12529305 PMC430948
- [31]Wiehe T. Gebauer-Jung S. Mitchell-Olds T. Guigo R. SGP-1: prediction and validation of homologous genes based on sequence alignments Genome Res. 2001 11 1574 1583 11544202 PMC311140
- [32]Parra G. Blanco E. Guigo R. GeneID in Drosophila Genome Res. 2000 10 511 515 10779490 PMC310871
- [33]Stanke M. Steinkamp R. Waack S. Morgenstern B. AUGUSTUS: a web server for gene finding in eukaryotes Nucleic Acids Res. 2004 32 W309 W312 15215400 PMC441517
- [34]Harrison P.M. Zheng D. Zhang Z. Carriero N. Gerstein M. Transcribed processed pseudogenes in the human genome: an intermediate form of expressed retrosequence lacking protein-coding ability Nucleic Acids Res. 2005 33 2374 2383 15860774 PMC1087782
- [35]Madera M. Vogel C. Kummerfeld S.K. Chothia C. Gough J. The SUPERFAMILY database in 2004: additions and improvements Nucleic Acids Res. 2004 32 D235 D239 14681402 PMC308851
- [36]Griffiths-Jones S. The microRNA registry Nucleic Acids Res. 2004 32 D109 D111 14681370 PMC308757
- [37]Weber M.J. New human and mouse microRNA genes found by homology search FEBS J. 2005 272 59 73 15634332
- [38]Drysdale R.A. Crosby M.A. FlyBase Consortium FlyBase: genes and gene models Nucleic Acids Res. 2005 33 D390 D395 15608223 PMC540000
- [39]Chen N. Harris T.W. Antoshechkin I. Bastiani C. Bieri T. Blasiar D. Bradnam K. Canaran P. Chan J. Chen C.-K. WormBase: a comprehensive data resource for Caenorhabditis biology and genomics Nucleic Acids Res. 2005 33 D383 D389 15608221 PMC540020
- [40]Christie K.R. Weng S. Balakrishnan R. Costanzo M.C. Dolinski K. Dwight S.S. Engel S.R. Feierbach B. Fisk D.G. Hirschman J.E. Saccharomyces Genome Database (SGD) provides tools to identify and analyze sequences from Saccharomyces cerevisiae and related sequences from other organisms Nucleic Acids Res. 2004 32 D311 D314 14681421 PMC308767
- [41]Su A.I. Cooke M.P. Ching K.A. Hakak Y. Walker J.R. Wiltshire T. Orth A.P. Vega R.G. Sapinoso L.M. Moqrich A. Large-scale analysis of the human and mouse transcriptomes Proc. Natl Acad. Sci. USA 2002 99 4465 4470 11904358 PMC123671
- [42]Su A.I. Wiltshire T. Batalov S. Lapp H. Ching K.A. Block D. Zhang J. Soden R. Hayakawa M. Kreiman G. A gene atlas of the mouse and human protein-encoding transcriptomes Proc. Natl Acad. Sci. USA 2004 101 6062 6067 15075390 PMC395923
- [43]Cheng J. Kapranov P. Drenkow J. Dike S. Brubaker S. Patel S. Long J. Stern D. Tammana H. Helt G. Transcriptional maps of 10 human chromosomes at 5-nucleotide resolution Science 2005 308 1149 1154 15790807
- [44]Rinn J.L. Rozowsky J.S. Laurenzi I.J. Petersen P.H. Zou K. Zhong W. Gerstein M. Snyder M. Major molecular differences between mammalian sexes are involved in drug metabolism and renal function Dev. Cell 2004 6 791 800 15177028
- [45]Davuluri R.V. Grosse I. Zhang M.Q. Computational identification of promoters and first exons in the human genome Nature Genet. 2001 29 412 417 11726928
- [46]Matys V. Fricke E. Geffers R. Gossling E. Haubrock M. Hehl R. Hornischer K. Karas D. Kel A.E. Kel-Margoulis O.V. TRANSFAC: transcriptional regulation, from patterns to profiles Nucleic Acids Res. 2003 31 374 378 12520026 PMC165555
- [47]Sherry S.T. Ward M.H. Kholodov M. Baker J. Phan L. Smigielski E.M. Sirotkin K. dbSNP: the NCBI database of genetic variation Nucleic Acids Res. 2001 29 308 311 11125122 PMC29783
- [48]Bailey J.A. Yavor A.M. Massa H.F. Trask B.J. Eichler E.E. Segmental duplications: organization and impact within the current human genome project assembly Genome Res. 2001 11 1005 1017 11381028 PMC311093
- [49]Iafrate A.J. Feuk L. Rivera M.N. Listewnik M.L. Donahoe P.K. Qi Y. Scherer S.W. Lee C. Detection of large-scale variation in the human genome Nature Genet. 2004 36 949 951 15286789
- [50]Sebat J. Lakshmi B. Troge J. Alexander J. Young J. Lundin P. Maner S. Massa H. Walker M. Chi M. Large-scale copy number polymorphism in the human genome Science 2004 305 525 528 15273396
- [51]Sharp A.J. Locke D.P. McGrath S.D. Cheng Z. Bailey J.A. Vallente R.U. Pertz L.M. Clark R.A. Schwartz S. Segraves R. Segmental duplications and copy-number variation in the human genome Am. J. Hum. Genet. 2005 77 78 88 15918152 PMC1226196
- [52]Tuzun E. Sharp A.J. Bailey J.A. Kaul R. Morrison V.A. Pertz L.M. Haugen E. Hayden H. Albertson D. Pinkel D. Fine-scale structural variation of the human genome Nature Genet. 2005 37 727 732 15895083
- [53]Roberts R.J. Vincze T. Posfai J. Macelis D. REBASE—restriction enzymes and DNA methyltransferases Nucleic Acids Res. 2005 33 D230 232 15608184 PMC539983
Cited by
Sorted by citations
Circular RNAs are a large class of animal RNAs with regulatory potency
Memczak, S., Jens, M., Elefsinioti, A., Torti, F., Krueger, J., Rybak, A., Maier, L., Mackowiak, S. D., Gregersen, L. H., Munschauer, M., et al. (2013) · Nature · doi:10.1038/nature11928 · Cited by 7,990 · see citing works
Circular RNAs in the Mammalian Brain Are Highly Abundant, Conserved, and Dynamically Expressed
Rybak-Wolf, A., Stottmeister, C., Glažar, P., Jens, M., Pino, N., Giusti, S., Hanan, M., Behm, M., Bartok, O., Ashwal-Fluss, R., et al. (2015) · Molecular Cell · doi:10.1016/j.molcel.2015.03.027 · Cited by 2,423 · see citing works
Expanded encyclopaedias of DNA elements in the human and mouse genomes
The ENCODE Project Consortium, Abascal, F., Acosta, R., Addleman, N. J., Adrian, J., Afzal, V., Ai, R., Aken, B., Akiyama, J. A., Jammal, O. A., et al. (2020) · Nature · doi:10.1038/s41586-020-2493-4 · Cited by 2,378 · see citing works
Global epigenomic reconfiguration during mammalian brain development
Lister, R., Mukamel, E. A., Nery, J. R., Urich, M., Puddifoot, C. A., Johnson, N. D., Lucero, J., Huang, Y., Dwork, A. J., Schultz, M. D., et al. (2013) · Science · doi:10.1126/science.1237905 · Cited by 1,830 · see citing works
Effective gene expression prediction from sequence by integrating long-range interactions
Avsec, Ž., Agarwal, V., Visentin, D., Ledsam, J. R., Grabska-Barwinska, A., Taylor, K. R., Assael, Y., Jumper, J., Kohli, P., & Kelley, D. R. (2021) · Nature Methods · doi:10.1038/s41592-021-01252-x · Cited by 1,326 · see citing works
VISTA Enhancer Browser—a database of tissue-specific human enhancers
Visel, A., Minovitsky, S., Dubchak, I., & Pennacchio, L. A. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkl822 · Cited by 1,080 · see citing works
Chromatin states define tumour-specific T cell dysfunction and reprogramming
Philip, M., Fairchild, L., Sun, L., Horste, E. L., Camara, S., Shakiba, M., Scott, A. C., Viale, A., Lauer, P., Merghoub, T., et al. (2017) · Nature · doi:10.1038/nature22367 · Cited by 933 · see citing works
A single-cell RNA-seq survey of the developmental landscape of the human prefrontal cortex
Zhong, S., Zhang, S., Fan, X., Wu, Q., Yan, L., Dong, J., Zhang, H., Li, L., Sun, L., Pan, N., et al. (2018) · Nature · doi:10.1038/nature25980 · Cited by 689 · see citing works
Pathway Tools version 13.0: integrated software for pathway/genome informatics and systems biology
Karp, P. D., Paley, S. M., Krummenacker, M., Latendresse, M., Dale, J. M., Lee, T. J., Kaipa, P., Gilham, F., Spaulding, A., Popescu, L., et al. (2010) · Briefings in Bioinformatics · doi:10.1093/bib/bbp043 · Cited by 694 · see citing works
Karp, P. D., Paley, S., & Romero, P. (2002) · Bioinformatics · doi:10.1093/bioinformatics/18.suppl_1.s225 · Cited by 661 · see citing works
Genomic views of distant-acting enhancers
Visel, A., Rubin, E. M., & Pennacchio, L. A. (2009) · Nature · doi:10.1038/nature08451 · Cited by 610 · see citing works
Conserved epigenomic signals in mice and humans reveal immune basis of Alzheimer's disease
Gjoneska, E., Pfenning, A. R., Mathys, H., Quon, G., Kundaje, A., Tsai, L.-H., & Kellis, M. (2015) · Nature · doi:10.1038/nature14252 · Cited by 576 · see citing works
AceView: a comprehensive cDNA-supported gene and transcripts annotation
Thierry-Mieg, D., & Thierry-Mieg, J. (2006) · Genome Biology · doi:10.1186/gb-2006-7-s1-s12 · Cited by 629 · see citing works
A complete reference genome improves analysis of human genetic variation
Aganezov, S., Yan, S. M., Soto, D. C., Kirsche, M., Zarate, S., Avdeyev, P., Taylor, D. J., Shafin, K., Shumate, A., Xiao, C., et al. (2022) · Science · doi:10.1126/science.abl3533 · Cited by 441 · see citing works
Hui, K. Y., Fernandez-Hernandez, H., Hu, J., Schaffner, A., Pankratz, N., Hsu, N.-Y., Chuang, L.-S., Carmi, S., Villaverde, N., Li, X., et al. (2018) · Science Translational Medicine · doi:10.1126/scitranslmed.aai7795 · Cited by 384 · see citing works
From telomere to telomere: The transcriptional and epigenetic state of human repeat elements
Hoyt, S. J., Storer, J. M., Hartley, G. A., Grady, P. G. S., Gershman, A., de Lima, L. G., Limouse, C., Halabian, R., Wojenski, L., Rodriguez, M., et al. (2022) · Science · doi:10.1126/science.abk3112 · Cited by 411 · see citing works
Genome-wide association study of obsessive-compulsive disorder
Stewart, S. E., Yu, D., Scharf, J. M., Neale, B. M., Fagerness, J. A., Mathews, C. A., Arnold, P. D., Evans, P. D., Gamazon, E. R., Osiecki, L., et al. (2013) · Molecular Psychiatry · doi:10.1038/mp.2012.85 · Cited by 384 · see citing works
Genome-wide profiling of heritable and de novo STR variations
Willems, T., Zielinski, D., Yuan, J., Gordon, A., Gymrek, M., & Erlich, Y. (2017) · Nature Methods · doi:10.1038/nmeth.4267 · Cited by 329 · see citing works
Systematic differences in discovery of genetic effects on gene expression and complex traits
Mostafavi, H., Spence, J. P., Naqvi, S., & Pritchard, J. K. (2023) · Nature Genetics · doi:10.1038/s41588-023-01529-1 · Cited by 336 · see citing works
Sey, N. Y. A., Hu, B., Mah, W., Fauni, H., McAfee, J. C., Rajarajan, P., Brennand, K. J., Akbarian, S., & Won, H. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-0603-0 · Cited by 297 · see citing works
Schizophrenia: a common disease caused by multiple rare alleles
McClellan, J. M., Susser, E., & King, M.-C. (2007) · British Journal of Psychiatry · doi:10.1192/bjp.bp.106.025585 · Cited by 296 · see citing works
Early Neolithic genomes from the eastern Fertile Crescent
Broushaki, F., Thomas, M. G., Link, V., López, S., van Dorp, L., Kirsanow, K., Hofmanová, Z., Diekmann, Y., Cassidy, L. M., Díez-del-Molino, D., et al. (2016) · Science · doi:10.1126/science.aaf7943 · Cited by 288 · see citing works
Molecular and cellular reorganization of neural circuits in the human lineage
Sousa, A. M. M., Zhu, Y., Raghanti, M. A., Kitchen, R. R., Onorati, M., Tebbenkamp, A. T. N., Stutz, B., Meyer, K. A., Li, M., Kawasawa, Y. I., et al. (2017) · Science · doi:10.1126/science.aan3456 · Cited by 253 · see citing works
Dannemann, M., Andrés, A. M., & Kelso, J. (2016) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2015.11.015 · Cited by 249 · see citing works
Swanson, E., Lord, C., Reading, J., Heubeck, A. T., Genge, P. C., Thomson, Z., Weiss, M. D., Li, X.-J., Savage, A. K., Green, R. R., et al. (2021) · eLife · doi:10.7554/elife.63632 · Cited by 267 · see citing works
Smith, A. K., Kilaru, V., Kocak, M., Almli, L. M., Mercer, K. B., Ressler, K. J., Tylavsky, F. A., & Conneely, K. N. (2014) · BMC Genomics · doi:10.1186/1471-2164-15-145 · Cited by 239 · see citing works
Hinds, D. A., McMahon, G., Kiefer, A. K., Do, C. B., Eriksson, N., Evans, D. M., St Pourcain, B., Ring, S. M., Mountain, J. L., Francke, U., et al. (2013) · Nature Genetics · doi:10.1038/ng.2686 · Cited by 246 · see citing works
Amaral, P. P., Neyt, C., Wilkins, S. J., Askarian-Amiri, M. E., Sunkin, S. M., Perkins, A. C., & Mattick, J. S. (2009) · RNA · doi:10.1261/rna.1705309 · Cited by 209 · see citing works
Widespread splicing changes in human brain development and aging
Mazin, P., Xiong, J., Liu, X., Yan, Z., Zhang, X., Li, M., He, L., Somel, M., Yuan, Y., Phoebe Chen, Y., et al. (2013) · Molecular Systems Biology · doi:10.1038/msb.2012.67 · Cited by 216 · see citing works
Recovery of trait heritability from whole genome sequence data
Wainschtein, P., Jain, D., Zheng, Z., TOPMed Anthropometry Working Group, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Cupples, L. A., Shadyab, A. H., McKnight, B., Shoemaker, B. M., Mitchell, B. D., et al. (2019) · doi:10.1101/588020 · Cited by 515 · see citing works
Kazachenka, A., Bertozzi, T. M., Sjoberg-Herrera, M. K., Walker, N., Gardner, J., Gunning, R., Pahita, E., Adams, S., Adams, D., & Ferguson-Smith, A. C. (2018) · Cell · doi:10.1016/j.cell.2018.09.043 · Cited by 181 · see citing works
Zona, L., Lupberger, J., Sidahmed-Adrar, N., Thumann, C., Harris, H. J., Barnes, A., Florentin, J., Tawar, R. G., Xiao, F., Turek, M., et al. (2013) · Cell Host & Microbe · doi:10.1016/j.chom.2013.02.006 · Cited by 182 · see citing works
Arnold, C. D., Gerlach, D., Spies, D., Matts, J. A., Sytnikova, Y. A., Pagani, M., Lau, N. C., & Stark, A. (2014) · Nature Genetics · doi:10.1038/ng.3009 · Cited by 175 · see citing works
Control of embryonic stem cell lineage commitment by core promoter factor, TAF3
Liu, Z., Scannell, D. R., Eisen, M. B., & Tjian, R. (2011) · Cell · doi:10.1016/j.cell.2011.08.005 · Cited by 167 · see citing works
Luo, Y., de Lange, K. M., Jostins, L., Moutsianas, L., Randall, J., Kennedy, N. A., Lamb, C. A., McCarthy, S., Ahmad, T., Edwards, C., et al. (2017) · Nature Genetics · doi:10.1038/ng.3761 · Cited by 162 · see citing works
Jaffe, A. E., Shin, J., Collado-Torres, L., Leek, J. T., Tao, R., Li, C., Gao, Y., Jia, Y., Maher, B. J., Hyde, T. M., et al. (2015) · Nature Neuroscience · doi:10.1038/nn.3898 · Cited by 156 · see citing works
Deletions of chromosomal regulatory boundaries are associated with congenital disease
Ibn-Salem, J., Köhler, S., Love, M. I., Chung, H.-R., Huang, N., Hurles, M. E., Haendel, M., Washington, N. L., Smedley, D., Mungall, C. J., et al. (2014) · Genome Biology · doi:10.1186/s13059-014-0423-1 · Cited by 143 · see citing works
LRPPRC-mediated folding of the mitochondrial transcriptome
Siira, S. J., Spåhr, H., Shearwood, A.-M. J., Ruzzenente, B., Larsson, N.-G., Rackham, O., & Filipovska, A. (2017) · Nature Communications · doi:10.1038/s41467-017-01221-z · Cited by 123 · see citing works
Functional coordination of alternative splicing in the mammalian central nervous system
Fagnani, M., Barash, Y., Ip, J. Y., Misquitta, C., Pan, Q., Saltzman, A. L., Shai, O., Lee, L., Rozenhek, A., Mohammad, N., et al. (2007) · Genome Biology · doi:10.1186/gb-2007-8-6-r108 · Cited by 120 · see citing works
Three-dimensional genome rewiring in loci with human accelerated regions
Keough, K. C., Whalen, S., Inoue, F., Przytycki, P. F., Fair, T., Deng, C., Steyert, M., Ryu, H., Lindblad-Toh, K., Karlsson, E., et al. (2023) · Science · doi:10.1126/science.abm1696 · Cited by 113 · see citing works
Evidence for additive and synergistic action of mammalian enhancers during cell fate determination
Choi, J., Lysakovskaia, K., Stik, G., Demel, C., Söding, J., Tian, T. V., Graf, T., & Cramer, P. (2021) · eLife · doi:10.7554/elife.65381 · Cited by 117 · see citing works
Identification of genetic variants influencing the human plasma proteome
Johansson, Å., Enroth, S., Palmblad, M., Deelder, A. M., Bergquist, J., & Gyllensten, U. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1217238110 · Cited by 82 · see citing works
de la Grange, P., Dutertre, M., Correa, M., & Auboeuf, D. (2007) · BMC Bioinformatics · doi:10.1186/1471-2105-8-180 · Cited by 78 · see citing works
Hawash, M. B. F., Sanz-Remón, J., Grenier, J.-C., Kohn, J., Yotova, V., Johnson, Z., Lanford, R. E., Brinkworth, J. F., & Barreiro, L. B. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2015855118 · Cited by 56 · see citing works
Kamath, M. B., Houston, I. B., Janovski, A. J., Zhu, X., Gowrisankar, S., Jegga, A. G., & DeKoter, R. P. (2008) · Leukemia · doi:10.1038/leu.2008.67 · Cited by 41 · see citing works
Naval-Sánchez, M., Porto-Neto, L. R., Cardoso, D. F., Hayes, B. J., Daetwyler, H. D., Kijas, J., & Reverter, A. (2020) · Genetics Selection Evolution · doi:10.1186/s12711-020-00546-6 · Cited by 43 · see citing works
SINEs, evolution and genome structure in the opossum
Gu, W., Ray, D. A., Walker, J. A., Barnes, E. W., Gentles, A. J., Samollow, P. B., Jurka, J., Batzer, M. A., & Pollock, D. D. (2007) · Gene · doi:10.1016/j.gene.2007.02.028 · Cited by 18 · see citing works
Goto, H., Watanabe, K., Araragi, N., Kageyama, R., Tanaka, K., Kuroki, Y., Toyoda, A., Hattori, M., Sakaki, Y., Fujiyama, A., et al. (2009) · BMC Evolutionary Biology · doi:10.1186/1471-2148-9-224 · Cited by 16 · see citing works
Molecular and cellular processes disrupted in the early postnatal Down syndrome prefrontal cortex
Risgaard, R. D., Hanthanan Arachchilage, K., Knaack, S. A., Hosseini, M., Chen, R. J., Kumarage, P., Schmidt, D. K., Huang, X., Sheng, J., Wang, C. J., et al. (2026) · Science · doi:10.1126/science.aea1549 · Cited by 12 · see citing works
Western, D., Yang, C., Timsina, J., Liu, M., Wang, C., Campbell, M. C., Kotzbauer, P., Perlmutter, J. S., Schindler, S. E., Morris, J. C., et al. (2026) · Science Translational Medicine · doi:10.1126/scitranslmed.adz2016 · Cited by 1 · see citing works
Wu, Q., Yang, F., An, Q., Liu, Y., Tian, H., Du, Y., Cai, W., Lei, M., Xu, J., Deng, L., et al. (2026) · Journal of the American Heart Association · doi:10.1161/jaha.126.049987
TFXcan reveals transcription factor programs driving GWAS loci
Adeluwa, T., Salazar-Magaña, S., Sumner, S., Gona, S., Nyasimi, F., Carbonetto, P., Baca, S. C., Freedman, M., Gusev, A., Liu, B., et al. (2026) · Cell Genomics · doi:10.1016/j.xgen.2026.101398
Mei, Y., Vad, O. B., Beyer, A. F., Ghouse, J., & Lundegaard, P. R. (2026) · Molecular & Cellular Proteomics · doi:10.1016/j.mcpro.2026.101692
- Authors
- Hinrichs, A. S.
- Affiliations
- University of California, Santa Cruz (US)
- Corresponding author
- Hinrichs, A. S.
- ORCID
- Hinrichs, A. S.
- Venue
- Nucleic Acids Research
- Publisher
- Oxford University Press (OUP)
- Published
- 2006-01-01
- Volume
- 34
- Issue
- 90001
- Pages
- D590-D598
- ISSN
- 0305-1048 (ISSN-L)
- 1362-4962
- PMC
- PMC1347506
- OpenAlex
- W2915985519
- Cited by
- 1,646
- References
- 4
- Citations by year
- 2026: 184 · 2025: 221 · 2024: 172 · 2023: 133 · 2022: 116 · 2021: 104 · 2020: 95 · 2019: 89 · 2018: 61 · 2017: 33 · 2016: 37 · 2015: 38 · 2014: 40 · 2013: 35 · 2012: 19
- FWCI
- 22.17
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- other-oa
- Locations
- Nucleic Acids Research (publishedVersion, other-oa)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Cold Spring Harbor Laboratory Institutional Repository (Cold Spring Harbor Laboratory) (acceptedVersion)
- Research at the University of Copenhagen (University of Copenhagen) (submittedVersion)
- Funders
- University of California, Santa Cruz
- National Institutes of Health
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genetics, Bioinformatics, and Biomedical Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
- Keywords
- UCSC Genome Browser, genome annotation, vertebrate genomes, model organisms, genome assembly, gene prediction, comparative genomics, gene expression, genetic variation, blat, in silico PCR
- MeSH terms
- Amino Acid Sequence, Animals, California, Computer Graphics, Dogs, Genes, Humans, Proteins, Software, User-Computer Interface, Gene Expression, Sequence Alignment, Internet, Polymorphism, Single Nucleotide, Genomics, Databases, Genetic, Proteomics, Mice, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review