RNAcentral: A vision for an international database of RNA sequences.
Bateman A, Agrawal S, Birney E, Bruford EA, Bujnicki JM, Cochrane G, Cole JR, Dinger ME, Enright AJ, Gardner PP, Gautheret D, Griffiths-Jones S, Harrow J, Herrero J, Holmes IH, Huang HD, Kelly KA, Kersey P, Kozomara A, Lowe TM, Marz M, Moxon S, Pruitt KD, Samuelsson T, Stadler PF, Vilella AJ, Vogel JH, Williams KP, Wright MW and Zwieb C
RNA (New York, N.Y.)2011;17;11;
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The origins, evolution, and functional potential of alternative splicing in vertebrates.
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Molecular biology and evolution2011;28;10;
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Mouse genomic variation and its effect on phenotypes and gene regulation.
Keane TM, Goodstadt L, Danecek P, White MA, Wong K, Yalcin B, Heger A, Agam A, Slater G, Goodson M, Furlotte NA, Eskin E, Nellåker C, Whitley H, Cleak J, Janowitz D, Hernandez-Pliego P, Edwards A, Belgard TG, Oliver PL, McIntyre RE, Bhomra A, Nicod J, Gan X, Yuan W, van der Weyden L, Steward CA, Bala S, Stalker J, Mott R, Durbin R, Jackson IJ, Czechanski A, Guerra-Assunção JA, Donahue LR, Reinholdt LG, Payseur BA, Ponting CP, Birney E, Flint J and Adams DJ
Nature2011;477;7364;
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Evidence that Cd101 is an autoimmune diabetes gene in nonobese diabetic mice.
Rainbow DB, Moule C, Fraser HI, Clark J, Howlett SK, Burren O, Christensen M, Moody V, Steward CA, Mohammed JP, Fusakio ME, Masteller EL, Finger EB, Houchins JP, Naf D, Koentgen F, Ridgway WM, Todd JA, Bluestone JA, Peterson LB, Mattner J and Wicker LS
Journal of immunology (Baltimore, Md. : 1950)2011;187;1;
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The GENCODE exome: sequencing the complete human exome.
Coffey AJ, Kokocinski F, Calafato MS, Scott CE, Palta P, Drury E, Joyce CJ, Leproust EM, Harrow J, Hunt S, Lehesjoki AE, Turner DJ, Hubbard TJ and Palotie A
European journal of human genetics : EJHG2011;19;7;
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A conditional knockout resource for the genome-wide study of mouse gene function.
Skarnes WC, Rosen B, West AP, Koutsourakis M, Bushell W, Iyer V, Mujica AO, Thomas M, Harrow J, Cox T, Jackson D, Severin J, Biggs P, Fu J, Nefedov M, de Jong PJ, Stewart AF and Bradley A
Nature2011;474;7351;
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Shotgun proteomics aids discovery of novel protein-coding genes, alternative splicing, and "resurrected" pseudogenes in the mouse genome.
Brosch M, Saunders GI, Frankish A, Collins MO, Yu L, Wright J, Verstraten R, Adams DJ, Harrow J, Choudhary JS and Hubbard T
Genome research2011;21;5;
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Gene inactivation and its implications for annotation in the era of personal genomics.
Balasubramanian S, Habegger L, Frankish A, MacArthur DG, Harte R, Tyler-Smith C, Harrow J and Gerstein M
Genes & development2011;25;1;
PUBMED: 21205862; PMC: 3012931; DOI: 10.1101/gad.1968411
The tammar wallaby major histocompatibility complex shows evidence of past genomic instability.
Siddle HV, Deakin JE, Coggill P, Whilming L, Harrow J, Kaufman J, Beck S and Belov K
BMC genomics2011;12;
PUBMED: 21854592; PMC: 3179965; DOI: 10.1186/1471-2164-12-421
Nonobese diabetic congenic strain analysis of autoimmune diabetes reveals genetic complexity of the Idd18 locus and identifies Vav3 as a candidate gene.
Fraser HI, Dendrou CA, Healy B, Rainbow DB, Howlett S, Smink LJ, Gregory S, Steward CA, Todd JA, Peterson LB and Wicker LS
Journal of immunology (Baltimore, Md. : 1950)2010;184;9;
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Genome-wide end-sequenced BAC resources for the NOD/MrkTac() and NOD/ShiLtJ() mouse genomes.
Steward CA, Humphray S, Plumb B, Jones MC, Quail MA, Rice S, Cox T, Davies R, Bonfield J, Keane TM, Nefedov M, de Jong PJ, Lyons P, Wicker L, Todd J, Hayashizaki Y, Gulban O, Danska J, Harrow J, Hubbard T, Rogers J and Adams DJ
Genomics2010;95;2;
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AnnoTrack--a tracking system for genome annotation.
Kokocinski F, Harrow J and Hubbard T
BMC genomics2010;11;
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Beyond the Genome: genomics research ten years after the human genome sequence.
Casto AM and Amid C
Genome biology2010;11;11;
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Identification and analysis of unitary pseudogenes: historic and contemporary gene losses in humans and other primates.
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Genome biology2010;11;3;
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Meeting report: a workshop on Best Practices in Genome Annotation.
Madupu R, Brinkac LM, Harrow J, Wilming LG, Böhme U, Lamesch P and Hannick LI
Database : the journal of biological databases and curation2010;2010;
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Quantifying the mechanisms of domain gain in animal proteins.
Buljan M, Frankish A and Bateman A
Genome biology2010;11;7;
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Discovery of candidate disease genes in ENU-induced mouse mutants by large-scale sequencing, including a splice-site mutation in nucleoredoxin.
Boles MK, Wilkinson BM, Wilming LG, Liu B, Probst FJ, Harrow J, Grafham D, Hentges KE, Woodward LP, Maxwell A, Mitchell K, Risley MD, Johnson R, Hirschi K, Lupski JR, Funato Y, Miki H, Marin-Garcia P, Matthews L, Coffey AJ, Parker A, Hubbard TJ, Rogers J, Bradley A, Adams DJ and Justice MJ
PLoS genetics2009;5;12;
PUBMED: 20011118; PMC: 2782131; DOI: 10.1371/journal.pgen.1000759
A novel system of polymorphic and diverse NK cell receptors in primates.
Averdam A, Petersen B, Rosner C, Neff J, Roos C, Eberle M, Aujard F, Münch C, Schempp W, Carrington M, Shiina T, Inoko H, Knaust F, Coggill P, Sehra H, Beck S, Abi-Rached L, Reinhardt R and Walter L
PLoS genetics2009;5;10;
PUBMED: 19834558; PMC: 2757895; DOI: 10.1371/journal.pgen.1000688
The consensus coding sequence (CCDS) project: Identifying a common protein-coding gene set for the human and mouse genomes.
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Genome research2009;19;7;
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The genome sequence of taurine cattle: a window to ruminant biology and evolution.
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Science (New York, N.Y.)2009;324;5926;
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Comparative analysis of processed ribosomal protein pseudogenes in four mammalian genomes.
Balasubramanian S, Zheng D, Liu YJ, Fang G, Frankish A, Carriero N, Robilotto R, Cayting P and Gerstein M
Genome biology2009;10;1;
PUBMED: 19123937; PMC: 2687790; DOI: 10.1186/gb-2009-10-1-r2
Identifying protein-coding genes in genomic sequences.
Harrow J, Nagy A, Reymond A, Alioto T, Patthy L, Antonarakis SE and Guigó R
Genome biology2009;10;1;
PUBMED: 19226436; PMC: 2687780; DOI: 10.1186/gb-2009-10-1-201
MHC-linked and un-linked class I genes in the wallaby.
Siddle HV, Deakin JE, Coggill P, Hart E, Cheng Y, Wong ES, Harrow J, Beck S and Belov K
BMC genomics2009;10;
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Manual annotation and analysis of the defensin gene cluster in the C57BL/6J mouse reference genome.
Amid C, Rehaume LM, Brown KL, Gilbert JG, Dougan G, Hancock RE and Harrow JL
BMC genomics2009;10;
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Conservation of the H19 noncoding RNA and H19-IGF2 imprinting mechanism in therians.
Smits G, Mungall AJ, Griffiths-Jones S, Smith P, Beury D, Matthews L, Rogers J, Pask AJ, Shaw G, VandeBerg JL, McCarrey JR, SAVOIR Consortium, Renfree MB, Reik W and Dunham I
Nature genetics2008;40;8;
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Efficient targeted transcript discovery via array-based normalization of RACE libraries.
Djebali S, Kapranov P, Foissac S, Lagarde J, Reymond A, Ucla C, Wyss C, Drenkow J, Dumais E, Murray RR, Lin C, Szeto D, Denoeud F, Calvo M, Frankish A, Harrow J, Makrythanasis P, Vidal M, Salehi-Ashtiani K, Antonarakis SE, Gingeras TR and Guigó R
Nature methods2008;5;7;
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The evolution of the DLK1-DIO3 imprinted domain in mammals.
Edwards CA, Mungall AJ, Matthews L, Ryder E, Gray DJ, Pask AJ, Shaw G, Graves JA, Rogers J, SAVOIR consortium, Dunham I, Renfree MB and Ferguson-Smith AC
PLoS biology2008;6;6;
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Determination and validation of principal gene products.
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Bioinformatics (Oxford, England)2008;24;1;
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The H-Invitational Database (H-InvDB), a comprehensive annotation resource for human genes and transcripts.
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Nucleic acids research2008;36;Database issue;
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The vertebrate genome annotation (Vega) database.
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Nucleic acids research2008;36;Database issue;
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Variation analysis and gene annotation of eight MHC haplotypes: the MHC Haplotype Project.
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Immunogenetics2008;60;1;
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Dynamic instability of the major urinary protein gene family revealed by genomic and phenotypic comparisons between C57 and 129 strain mice.
Mudge JM, Armstrong SD, McLaren K, Beynon RJ, Hurst JL, Nicholson C, Robertson DH, Wilming LG and Harrow JL
Genome biology2008;9;5;
PUBMED: 18507838; PMC: 2441477; DOI: 10.1186/gb-2008-9-5-r91
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project.
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Nature2007;447;7146;
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Prominent use of distal 5' transcription start sites and discovery of a large number of additional exons in ENCODE regions.
Denoeud F, Kapranov P, Ucla C, Frankish A, Castelo R, Drenkow J, Lagarde J, Alioto T, Manzano C, Chrast J, Dike S, Wyss C, Henrichsen CN, Holroyd N, Dickson MC, Taylor R, Hance Z, Foissac S, Myers RM, Rogers J, Hubbard T, Harrow J, Guigó R, Gingeras TR, Antonarakis SE and Reymond A
Genome research2007;17;6;
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Pseudogenes in the ENCODE regions: consensus annotation, analysis of transcription, and evolution.
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Genome research2007;17;6;
PUBMED: 17568002; PMC: 1891343; DOI: 10.1101/gr.5586307
The implications of alternative splicing in the ENCODE protein complement.
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Proceedings of the National Academy of Sciences of the United States of America2007;104;13;
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A high utility integrated map of the pig genome.
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Genome biology2007;8;7;
PUBMED: 17625002; PMC: 2323232; DOI: 10.1186/gb-2007-8-7-r139
Lessons learned from the initial sequencing of the pig genome: comparative analysis of an 8 Mb region of pig chromosome 17.
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Genome biology2007;8;8;
PUBMED: 17705864; PMC: 2374978; DOI: 10.1186/gb-2007-8-8-r168
The LRC haplotype project: a resource for killer immunoglobulin-like receptor-linked association studies.
Horton R, Coggill P, Miretti MM, Sambrook JG, Traherne JA, Ward R, Sims S, Palmer S, Sehra H, Harrow J, Rogers J, Carrington M, Trowsdale J and Beck S
Tissue antigens2006;68;5;
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The genomic sequence and analysis of the swine major histocompatibility complex.
Renard C, Hart E, Sehra H, Beasley H, Coggill P, Howe K, Harrow J, Gilbert J, Sims S, Rogers J, Ando A, Shigenari A, Shiina T, Inoko H, Chardon P and Beck S
Genomics2006;88;1;
PUBMED: 16515853; DOI: 10.1016/j.ygeno.2006.01.004
Identification of a single killer immunoglobulin-like receptor (KIR) gene in the porcine leukocyte receptor complex on chromosome 6q.
Sambrook JG, Sehra H, Coggill P, Humphray S, Palmer S, Sims S, Takamatsu HH, Wileman T, Archibald AL and Beck S
Immunogenetics 2006;58;5-6;
PUBMED: 16738944; DOI: 10.1007/s00251-006-0110-9
The DNA sequence and biological annotation of human chromosome 1.
Gregory SG, Barlow KF, McLay KE, Kaul R, Swarbreck D, Dunham A, Scott CE, Howe KL, Woodfine K, Spencer CC, Jones MC, Gillson C, Searle S, Zhou Y, Kokocinski F, McDonald L, Evans R, Phillips K, Atkinson A, Cooper R, Jones C, Hall RE, Andrews TD, Lloyd C, Ainscough R, Almeida JP, Ambrose KD, Anderson F, Andrew RW, Ashwell RI, Aubin K, Babbage AK, Bagguley CL, Bailey J, Beasley H, Bethel G, Bird CP, Bray-Allen S, Brown JY, Brown AJ, Buckley D, Burton J, Bye J, Carder C, Chapman JC, Clark SY, Clarke G, Clee C, Cobley V, Collier RE, Corby N, Coville GJ, Davies J, Deadman R, Dunn M, Earthrowl M, Ellington AG, Errington H, Frankish A, Frankland J, French L, Garner P, Garnett J, Gay L, Ghori MR, Gibson R, Gilby LM, Gillett W, Glithero RJ, Grafham DV, Griffiths C, Griffiths-Jones S, Grocock R, Hammond S, Harrison ES, Hart E, Haugen E, Heath PD, Holmes S, Holt K, Howden PJ, Hunt AR, Hunt SE, Hunter G, Isherwood J, James R, Johnson C, Johnson D, Joy A, Kay M, Kershaw JK, Kibukawa M, Kimberley AM, King A, Knights AJ, Lad H, Laird G, Lawlor S, Leongamornlert DA, Lloyd DM, Loveland J, Lovell J, Lush MJ, Lyne R, Martin S, Mashreghi-Mohammadi M, Matthews L, Matthews NS, McLaren S, Milne S, Mistry S, Moore MJ, Nickerson T, O'Dell CN, Oliver K, Palmeiri A, Palmer SA, Parker A, Patel D, Pearce AV, Peck AI, Pelan S, Phelps K, Phillimore BJ, Plumb R, Rajan J, Raymond C, Rouse G, Saenphimmachak C, Sehra HK, Sheridan E, Shownkeen R, Sims S, Skuce CD, Smith M, Steward C, Subramanian S, Sycamore N, Tracey A, Tromans A, Van Helmond Z, Wall M, Wallis JM, White S, Whitehead SL, Wilkinson JE, Willey DL, Williams H, Wilming L, Wray PW, Wu Z, Coulson A, Vaudin M, Sulston JE, Durbin R, Hubbard T, Wooster R, Dunham I, Carter NP, McVean G, Ross MT, Harrow J, Olson MV, Beck S, Rogers J, Bentley DR, Banerjee R, Bryant SP, Burford DC, Burrill WD, Clegg SM, Dhami P, Dovey O, Faulkner LM, Gribble SM, Langford CF, Pandian RD, Porter KM and Prigmore E
Nature2006;441;7091;
PUBMED: 16710414; DOI: 10.1038/nature04727
DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage.
Zody MC, Garber M, Adams DJ, Sharpe T, Harrow J, Lupski JR, Nicholson C, Searle SM, Wilming L, Young SK, Abouelleil A, Allen NR, Bi W, Bloom T, Borowsky ML, Bugalter BE, Butler J, Chang JL, Chen CK, Cook A, Corum B, Cuomo CA, de Jong PJ, DeCaprio D, Dewar K, FitzGerald M, Gilbert J, Gibson R, Gnerre S, Goldstein S, Grafham DV, Grocock R, Hafez N, Hagopian DS, Hart E, Norman CH, Humphray S, Jaffe DB, Jones M, Kamal M, Khodiyar VK, LaButti K, Laird G, Lehoczky J, Liu X, Lokyitsang T, Loveland J, Lui A, Macdonald P, Major JE, Matthews L, Mauceli E, McCarroll SA, Mihalev AH, Mudge J, Nguyen C, Nicol R, O'Leary SB, Osoegawa K, Schwartz DC, Shaw-Smith C, Stankiewicz P, Steward C, Swarbreck D, Venkataraman V, Whittaker CA, Yang X, Zimmer AR, Bradley A, Hubbard T, Birren BW, Rogers J, Lander ES and Nusbaum C
Nature2006;440;7087;
PUBMED: 16625196; PMC: 2610434; DOI: 10.1038/nature04689
Pseudo-messenger RNA: phantoms of the transcriptome.
Frith MC, Wilming LG, Forrest A, Kawaji H, Tan SL, Wahlestedt C, Bajic VB, Kai C, Kawai J, Carninci P, Hayashizaki Y, Bailey TL and Huminiecki L
PLoS genetics2006;2;4;
PUBMED: 16683022; PMC: 1449882; DOI: 10.1371/journal.pgen.0020023
Genomic anatomy of the Tyrp1 (brown) deletion complex.
Smyth IM, Wilming L, Lee AW, Taylor MS, Gautier P, Barlow K, Wallis J, Martin S, Glithero R, Phillimore B, Pelan S, Andrew R, Holt K, Taylor R, McLaren S, Burton J, Bailey J, Sims S, Squares J, Plumb B, Joy A, Gibson R, Gilbert J, Hart E, Laird G, Loveland J, Mudge J, Steward C, Swarbreck D, Harrow J, North P, Leaves N, Greystrong J, Coppola M, Manjunath S, Campbell M, Smith M, Strachan G, Tofts C, Boal E, Cobley V, Hunter G, Kimberley C, Thomas D, Cave-Berry L, Weston P, Botcherby MR, White S, Edgar R, Cross SH, Irvani M, Hummerich H, Simpson EH, Johnson D, Hunsicker PR, Little PF, Hubbard T, Campbell RD, Rogers J and Jackson IJ
Proceedings of the National Academy of Sciences of the United States of America2006;103;10;
PUBMED: 16505357; PMC: 1450144; DOI: 10.1073/pnas.0600199103
Genetic analysis of completely sequenced disease-associated MHC haplotypes identifies shuffling of segments in recent human history.
Traherne JA, Horton R, Roberts AN, Miretti MM, Hurles ME, Stewart CA, Ashurst JL, Atrazhev AM, Coggill P, Palmer S, Almeida J, Sims S, Wilming LG, Rogers J, de Jong PJ, Carrington M, Elliott JF, Sawcer S, Todd JA, Trowsdale J and Beck S
PLoS genetics2006;2;1;
PUBMED: 16440057; PMC: 1331980; DOI: 10.1371/journal.pgen.0020009
EGASP: the human ENCODE Genome Annotation Assessment Project.
Guigó R, Flicek P, Abril JF, Reymond A, Lagarde J, Denoeud F, Antonarakis S, Ashburner M, Bajic VB, Birney E, Castelo R, Eyras E, Ucla C, Gingeras TR, Harrow J, Hubbard T, Lewis SE and Reese MG
Genome biology2006;7 Suppl 1;
PUBMED: 16925836; PMC: 1810551; DOI: 10.1186/gb-2006-7-s1-s2
GENCODE: producing a reference annotation for ENCODE.
Harrow J, Denoeud F, Frankish A, Reymond A, Chen CK, Chrast J, Lagarde J, Gilbert JG, Storey R, Swarbreck D, Rossier C, Ucla C, Hubbard T, Antonarakis SE and Guigo R
Genome biology2006;7 Suppl 1;
PUBMED: 16925838; PMC: 1810553; DOI: 10.1186/gb-2006-7-s1-s4
Performance assessment of promoter predictions on ENCODE regions in the EGASP experiment.
Bajic VB, Brent MR, Brown RH, Frankish A, Harrow J, Ohler U, Solovyev VV and Tan SL
Genome biology2006;7 Suppl 1;
PUBMED: 16925837; PMC: 1810552; DOI: 10.1186/gb-2006-7-s1-s3
Validation of mRNA/EST-based gene predictions in human Xp11.4 revealed differences to the organization of the orthologous mouse locus.
Wen G, Ramser J, Taudien S, Gausmann U, Blechschmidt K, Frankish A, Ashurst J, Meindl A and Platzer M
Mammalian genome : official journal of the International Mammalian Genome Society2005;16;12;
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The transcriptional landscape of the mammalian genome.
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Science (New York, N.Y.)2005;309;5740;
PUBMED: 16141072; DOI: 10.1126/science.1112014
VEGA, the genome browser with a difference.
Loveland J
Briefings in bioinformatics2005;6;2;
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The DNA sequence of the human X chromosome.
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Nature2005;434;7031;
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The Vertebrate Genome Annotation (Vega) database.
Ashurst JL, Chen CK, Gilbert JG, Jekosch K, Keenan S, Meidl P, Searle SM, Stalker J, Storey R, Trevanion S, Wilming L and Hubbard T
Nucleic acids research2005;33;Database issue;
PUBMED: 15608237; PMC: 540089; DOI: 10.1093/nar/gki135
Genomic sequence of the class II region of the canine MHC: comparison with the MHC of other mammalian species.
Debenham SL, Hart EA, Ashurst JL, Howe KL, Quail MA, Ollier WE and Binns MM
Genomics2005;85;1;
PUBMED: 15607421; DOI: 10.1016/j.ygeno.2004.09.009
Gene map of the extended human MHC.
Horton R, Wilming L, Rand V, Lovering RC, Bruford EA, Khodiyar VK, Lush MJ, Povey S, Talbot CC, Wright MW, Wain HM, Trowsdale J, Ziegler A and Beck S
Nature reviews. Genetics 2004;5;12;
PUBMED: 15573121; DOI: 10.1038/nrg1489
The ENCODE (ENCyclopedia Of DNA Elements) Project.
ENCODE Project Consortium
Science (New York, N.Y.)2004;306;5696;
PUBMED: 15499007; DOI: 10.1126/science.1105136
Identification of mammalian microRNA host genes and transcription units.
Rodriguez A, Griffiths-Jones S, Ashurst JL and Bradley A
Genome research2004;14;10A;
PUBMED: 15364901; PMC: 524413; DOI: 10.1101/gr.2722704
Organization and evolution of a gene-rich region of the mouse genome: a 12.7-Mb region deleted in the Del(13)Svea36H mouse.
Mallon AM, Wilming L, Weekes J, Gilbert JG, Ashurst J, Peyrefitte S, Matthews L, Cadman M, McKeone R, Sellick CA, Arkell R, Botcherby MR, Strivens MA, Campbell RD, Gregory S, Denny P, Hancock JM, Rogers J and Brown SD
Genome research2004;14;10A;
PUBMED: 15364904; PMC: 524412; DOI: 10.1101/gr.2478604
Complete MHC haplotype sequencing for common disease gene mapping.
Stewart CA, Horton R, Allcock RJ, Ashurst JL, Atrazhev AM, Coggill P, Dunham I, Forbes S, Halls K, Howson JM, Humphray SJ, Hunt S, Mungall AJ, Osoegawa K, Palmer S, Roberts AN, Rogers J, Sims S, Wang Y, Wilming LG, Elliott JF, de Jong PJ, Sawcer S, Todd JA, Trowsdale J and Beck S
Genome research2004;14;6;
PUBMED: 15140828; PMC: 419796; DOI: 10.1101/gr.2188104
Integrative annotation of 21,037 human genes validated by full-length cDNA clones.
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PLoS biology2004;2;6;
PUBMED: 15103394; PMC: 393292; DOI: 10.1371/journal.pbio.0020162
DNA sequence and analysis of human chromosome 9.
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Nature2004;429;6990;
PUBMED: 15164053; PMC: 2734081; DOI: 10.1038/nature02465
The DNA sequence and comparative analysis of human chromosome 10.
Deloukas P, Earthrowl ME, Grafham DV, Rubenfield M, French L, Steward CA, Sims SK, Jones MC, Searle S, Scott C, Howe K, Hunt SE, Andrews TD, Gilbert JG, Swarbreck D, Ashurst JL, Taylor A, Battles J, Bird CP, Ainscough R, Almeida JP, Ashwell RI, Ambrose KD, Babbage AK, Bagguley CL, Bailey J, Banerjee R, Bates K, Beasley H, Bray-Allen S, Brown AJ, Brown JY, Burford DC, Burrill W, Burton J, Cahill P, Camire D, Carter NP, Chapman JC, Clark SY, Clarke G, Clee CM, Clegg S, Corby N, Coulson A, Dhami P, Dutta I, Dunn M, Faulkner L, Frankish A, Frankland JA, Garner P, Garnett J, Gribble S, Griffiths C, Grocock R, Gustafson E, Hammond S, Harley JL, Hart E, Heath PD, Ho TP, Hopkins B, Horne J, Howden PJ, Huckle E, Hynds C, Johnson C, Johnson D, Kana A, Kay M, Kimberley AM, Kershaw JK, Kokkinaki M, Laird GK, Lawlor S, Lee HM, Leongamornlert DA, Laird G, Lloyd C, Lloyd DM, Loveland J, Lovell J, McLaren S, McLay KE, McMurray A, Mashreghi-Mohammadi M, Matthews L, Milne S, Nickerson T, Nguyen M, Overton-Larty E, Palmer SA, Pearce AV, Peck AI, Pelan S, Phillimore B, Porter K, Rice CM, Rogosin A, Ross MT, Sarafidou T, Sehra HK, Shownkeen R, Skuce CD, Smith M, Standring L, Sycamore N, Tester J, Thorpe A, Torcasso W, Tracey A, Tromans A, Tsolas J, Wall M, Walsh J, Wang H, Weinstock K, West AP, Willey DL, Whitehead SL, Wilming L, Wray PW, Young L, Chen Y, Lovering RC, Moschonas NK, Siebert R, Fechtel K, Bentley D, Durbin R, Hubbard T, Doucette-Stamm L, Beck S, Smith DR and Rogers J
Nature2004;429;6990;
PUBMED: 15164054; DOI: 10.1038/nature02462
The DNA sequence and analysis of human chromosome 13.
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Nature2004;428;6982;
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Polymorphic segmental duplications at 8p23.1 challenge the determination of individual defensin gene repertoires and the assembly of a contiguous human reference sequence.
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