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Results: 1 to 20 of 73

1.

Closing gaps in the human genome using sequencing by synthesis.

Garber M, Zody MC, Arachchi HM, Berlin A, Gnerre S, Green LM, Lennon N, Nusbaum C.

Genome Biol. 2009;10(6):R60. doi: 10.1186/gb-2009-10-6-r60. Epub 2009 Jun 2. Erratum in: Genome Biol. 2011;12(4):403.

PMID:
19490611
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Closing gaps in the human genome with fosmid resources generated from multiple individuals.

Bovee D, Zhou Y, Haugen E, Wu Z, Hayden HS, Gillett W, Tuzun E, Cooper GM, Sampas N, Phelps K, Levy R, Morrison VA, Sprague J, Jewett D, Buckley D, Subramaniam S, Chang J, Smith DR, Olson MV, Eichler EE, Kaul R.

Nat Genet. 2008 Jan;40(1):96-101. Epub 2007 Dec 23.

PMID:
18157130
[PubMed - indexed for MEDLINE]
3.

Finishing the finished human chromosome 22 sequence.

Cole CG, McCann OT, Collins JE, Oliver K, Willey D, Gribble SM, Yang F, McLaren K, Rogers J, Ning Z, Beare DM, Dunham I.

Genome Biol. 2008;9(5):R78. doi: 10.1186/gb-2008-9-5-r78. Epub 2008 May 13.

PMID:
18477386
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Closing the gaps on human chromosome 19 revealed genes with a high density of repetitive tandemly arrayed elements.

Leem SH, Kouprina N, Grimwood J, Kim JH, Mullokandov M, Yoon YH, Chae JY, Morgan J, Lucas S, Richardson P, Detter C, Glavina T, Rubin E, Barrett JC, Larionov V.

Genome Res. 2004 Feb;14(2):239-46. Epub 2004 Jan 12.

PMID:
14718380
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Finishing the euchromatic sequence of the human genome.

International Human Genome Sequencing Consortium.

Nature. 2004 Oct 21;431(7011):931-45.

PMID:
15496913
[PubMed - indexed for MEDLINE]
6.

Sequence and expression analysis of gaps in human chromosome 20.

Minocherhomji S, Seemann S, Mang Y, El-Schich Z, Bak M, Hansen C, Papadopoulos N, Josefsen K, Nielsen H, Gorodkin J, Tommerup N, Silahtaroglu A.

Nucleic Acids Res. 2012 Aug;40(14):6660-72. Epub 2012 Apr 17.

PMID:
22510267
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

The sequence of the human genome.

Venter JC, Adams MD, Myers EW, Li PW, Mural RJ, Sutton GG, Smith HO, Yandell M, Evans CA, Holt RA, Gocayne JD, Amanatides P, Ballew RM, Huson DH, Wortman JR, Zhang Q, Kodira CD, Zheng XH, Chen L, Skupski M, Subramanian G, Thomas PD, Zhang J, Gabor Miklos GL, Nelson C, Broder S, Clark AG, Nadeau J, McKusick VA, Zinder N, Levine AJ, Roberts RJ, Simon M, Slayman C, Hunkapiller M, Bolanos R, Delcher A, Dew I, Fasulo D, Flanigan M, Florea L, Halpern A, Hannenhalli S, Kravitz S, Levy S, Mobarry C, Reinert K, Remington K, Abu-Threideh J, Beasley E, Biddick K, Bonazzi V, Brandon R, Cargill M, Chandramouliswaran I, Charlab R, Chaturvedi K, Deng Z, Di Francesco V, Dunn P, Eilbeck K, Evangelista C, Gabrielian AE, Gan W, Ge W, Gong F, Gu Z, Guan P, Heiman TJ, Higgins ME, Ji RR, Ke Z, Ketchum KA, Lai Z, Lei Y, Li Z, Li J, Liang Y, Lin X, Lu F, Merkulov GV, Milshina N, Moore HM, Naik AK, Narayan VA, Neelam B, Nusskern D, Rusch DB, Salzberg S, Shao W, Shue B, Sun J, Wang Z, Wang A, Wang X, Wang J, Wei M, Wides R, Xiao C, Yan C, Yao A, Ye J, Zhan M, Zhang W, Zhang H, Zhao Q, Zheng L, Zhong F, Zhong W, Zhu S, Zhao S, Gilbert D, Baumhueter S, Spier G, Carter C, Cravchik A, Woodage T, Ali F, An H, Awe A, Baldwin D, Baden H, Barnstead M, Barrow I, Beeson K, Busam D, Carver A, Center A, Cheng ML, Curry L, Danaher S, Davenport L, Desilets R, Dietz S, Dodson K, Doup L, Ferriera S, Garg N, Gluecksmann A, Hart B, Haynes J, Haynes C, Heiner C, Hladun S, Hostin D, Houck J, Howland T, Ibegwam C, Johnson J, Kalush F, Kline L, Koduru S, Love A, Mann F, May D, McCawley S, McIntosh T, McMullen I, Moy M, Moy L, Murphy B, Nelson K, Pfannkoch C, Pratts E, Puri V, Qureshi H, Reardon M, Rodriguez R, Rogers YH, Romblad D, Ruhfel B, Scott R, Sitter C, Smallwood M, Stewart E, Strong R, Suh E, Thomas R, Tint NN, Tse S, Vech C, Wang G, Wetter J, Williams S, Williams M, Windsor S, Winn-Deen E, Wolfe K, Zaveri J, Zaveri K, Abril JF, Guigó R, Campbell MJ, Sjolander KV, Karlak B, Kejariwal A, Mi H, Lazareva B, Hatton T, Narechania A, Diemer K, Muruganujan A, Guo N, Sato S, Bafna V, Istrail S, Lippert R, Schwartz R, Walenz B, Yooseph S, Allen D, Basu A, Baxendale J, Blick L, Caminha M, Carnes-Stine J, Caulk P, Chiang YH, Coyne M, Dahlke C, Mays A, Dombroski M, Donnelly M, Ely D, Esparham S, Fosler C, Gire H, Glanowski S, Glasser K, Glodek A, Gorokhov M, Graham K, Gropman B, Harris M, Heil J, Henderson S, Hoover J, Jennings D, Jordan C, Jordan J, Kasha J, Kagan L, Kraft C, Levitsky A, Lewis M, Liu X, Lopez J, Ma D, Majoros W, McDaniel J, Murphy S, Newman M, Nguyen T, Nguyen N, Nodell M, Pan S, Peck J, Peterson M, Rowe W, Sanders R, Scott J, Simpson M, Smith T, Sprague A, Stockwell T, Turner R, Venter E, Wang M, Wen M, Wu D, Wu M, Xia A, Zandieh A, Zhu X.

Science. 2001 Feb 16;291(5507):1304-51. Erratum in: Science 2001 Jun 5;292(5523):1838.

PMID:
11181995
[PubMed - indexed for MEDLINE]
8.

Finishing a whole-genome shotgun: release 3 of the Drosophila melanogaster euchromatic genome sequence.

Celniker SE, Wheeler DA, Kronmiller B, Carlson JW, Halpern A, Patel S, Adams M, Champe M, Dugan SP, Frise E, Hodgson A, George RA, Hoskins RA, Laverty T, Muzny DM, Nelson CR, Pacleb JM, Park S, Pfeiffer BD, Richards S, Sodergren EJ, Svirskas R, Tabor PE, Wan K, Stapleton M, Sutton GG, Venter C, Weinstock G, Scherer SE, Myers EW, Gibbs RA, Rubin GM.

Genome Biol. 2002;3(12):RESEARCH0079. Epub 2002 Dec 23.

PMID:
12537568
[PubMed - indexed for MEDLINE]
Free PMC Article
9.
10.

Automated finishing with autofinish.

Gordon D, Desmarais C, Green P.

Genome Res. 2001 Apr;11(4):614-25.

PMID:
11282977
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X.

Bentley DR, Deloukas P, Dunham A, French L, Gregory SG, Humphray SJ, Mungall AJ, Ross MT, Carter NP, Dunham I, Scott CE, Ashcroft KJ, Atkinson AL, Aubin K, Beare DM, Bethel G, Brady N, Brook JC, Burford DC, Burrill WD, Burrows C, Butler AP, Carder C, Catanese JJ, Clee CM, Clegg SM, Cobley V, Coffey AJ, Cole CG, Collins JE, Conquer JS, Cooper RA, Culley KM, Dawson E, Dearden FL, Durbin RM, de Jong PJ, Dhami PD, Earthrowl ME, Edwards CA, Evans RS, Gillson CJ, Ghori J, Green L, Gwilliam R, Halls KS, Hammond S, Harper GL, Heathcott RW, Holden JL, Holloway E, Hopkins BL, Howard PJ, Howell GR, Huckle EJ, Hughes J, Hunt PJ, Hunt SE, Izmajlowicz M, Jones CA, Joseph SS, Laird G, Langford CF, Lehvaslaiho MH, Leversha MA, McCann OT, McDonald LM, McDowall J, Maslen GL, Mistry D, Moschonas NK, Neocleous V, Pearson DM, Phillips KJ, Porter KM, Prathalingam SR, Ramsey YH, Ranby SA, Rice CM, Rogers J, Rogers LJ, Sarafidou T, Scott DJ, Sharp GJ, Shaw-Smith CJ, Smink LJ, Soderlund C, Sotheran EC, Steingruber HE, Sulston JE, Taylor A, Taylor RG, Thorpe AA, Tinsley E, Warry GL, Whittaker A, Whittaker P, Williams SH, Wilmer TE, Wooster R, Wright CL.

Nature. 2001 Feb 15;409(6822):942-3.

PMID:
11237015
[PubMed - indexed for MEDLINE]
12.

Nucleotide sequence surrounding the locus marker D21S246 on human chromosome 21.

Yamazaki M, Ono A, Watanabe K, Sasaki K, Tashiro H, Nomura T.

DNA Res. 1995 Aug 31;2(4):187-9.

PMID:
8590283
[PubMed - indexed for MEDLINE]
Free Article
13.

Human chromosome 7 circa 2004: a model for structural and functional studies of the human genome.

Scherer SW, Green ED.

Hum Mol Genet. 2004 Oct 1;13 Spec No 2:R303-13. Review.

PMID:
15358738
[PubMed - indexed for MEDLINE]
Free Article
14.

On the sequencing of the human genome.

Waterston RH, Lander ES, Sulston JE.

Proc Natl Acad Sci U S A. 2002 Mar 19;99(6):3712-6. Epub 2002 Mar 5.

PMID:
11880605
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Sequencing a genome by walking with clone-end sequences: a mathematical analysis.

Batzoglou S, Berger B, Mesirov J, Lander ES.

Genome Res. 1999 Dec;9(12):1163-74.

PMID:
10613838
[PubMed - indexed for MEDLINE]
Free Article
16.

Polymorphic segmental duplications at 8p23.1 challenge the determination of individual defensin gene repertoires and the assembly of a contiguous human reference sequence.

Taudien S, Galgoczy P, Huse K, Reichwald K, Schilhabel M, Szafranski K, Shimizu A, Asakawa S, Frankish A, Loncarevic IF, Shimizu N, Siddiqui R, Platzer M.

BMC Genomics. 2004 Dec 10;5(1):92.

PMID:
15588320
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

NotI flanking sequences: a tool for gene discovery and verification of the human genome.

Kutsenko AS, Gizatullin RZ, Al-Amin AN, Wang F, Kvasha SM, Podowski RM, Matushkin YG, Gyanchandani A, Muravenko OV, Levitsky VG, Kolchanov NA, Protopopov AI, Kashuba VI, Kisselev LL, Wasserman W, Wahlestedt C, Zabarovsky ER.

Nucleic Acids Res. 2002 Jul 15;30(14):3163-70.

PMID:
12136098
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Parking strategies for genome sequencing.

Roach JC, Thorsson V, Siegel AF.

Genome Res. 2000 Jul;10(7):1020-30.

PMID:
10899151
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Sequence-based, in situ detection of chromosomal abnormalities at high resolution.

Knoll JH, Rogan PK.

Am J Med Genet A. 2003 Sep 1;121A(3):245-57.

PMID:
12923866
[PubMed - indexed for MEDLINE]
20.

Construction and analysis of a human-chimpanzee comparative clone map.

Fujiyama A, Watanabe H, Toyoda A, Taylor TD, Itoh T, Tsai SF, Park HS, Yaspo ML, Lehrach H, Chen Z, Fu G, Saitou N, Osoegawa K, de Jong PJ, Suto Y, Hattori M, Sakaki Y.

Science. 2002 Jan 4;295(5552):131-4.

PMID:
11778049
[PubMed - indexed for MEDLINE]
Free Article

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