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Items: 20


Genomic survey sequencing for development and validation of single-locus SSR markers in peanut (Arachis hypogaea L.).

Zhou X, Dong Y, Zhao J, Huang L, Ren X, Chen Y, Huang S, Liao B, Lei Y, Yan L, Jiang H.

BMC Genomics. 2016 Jun 1;17:420. doi: 10.1186/s12864-016-2743-x.


Genome sequencing and comparative genomics of the broad host-range pathogen Rhizoctonia solani AG8.

Hane JK, Anderson JP, Williams AH, Sperschneider J, Singh KB.

PLoS Genet. 2014 May 8;10(5):e1004281. doi: 10.1371/journal.pgen.1004281.


Expedited batch processing and analysis of transposon insertions.

Smith JD, Ray DA.

BMC Res Notes. 2011 Nov 4;4:482. doi: 10.1186/1756-0500-4-482.


QTL global meta-analysis: are trait determining genes clustered?

Salih H, Adelson DL.

BMC Genomics. 2009 Apr 24;10:184. doi: 10.1186/1471-2164-10-184.


Understanding the development of human bladder cancer by using a whole-organ genomic mapping strategy.

Majewski T, Lee S, Jeong J, Yoon DS, Kram A, Kim MS, Tuziak T, Bondaruk J, Lee S, Park WS, Tang KS, Chung W, Shen L, Ahmed SS, Johnston DA, Grossman HB, Dinney CP, Zhou JH, Harris RA, Snyder C, Filipek S, Narod SA, Watson P, Lynch HT, Gazdar A, Bar-Eli M, Wu XF, McConkey DJ, Baggerly K, Issa JP, Benedict WF, Scherer SE, Czerniak B.

Lab Invest. 2008 Jul;88(7):694-721. doi: 10.1038/labinvest.2008.27.


Systematic recovery and analysis of full-ORF human cDNA clones.

Baross A, Butterfield YS, Coughlin SM, Zeng T, Griffith M, Griffith OL, Petrescu AS, Smailus DE, Khattra J, McDonald HL, McKay SJ, Moksa M, Holt RA, Marra MA.

Genome Res. 2004 Oct;14(10B):2083-92.


A web server for performing electronic PCR.

Rotmistrovsky K, Jang W, Schuler GD.

Nucleic Acids Res. 2004 Jul 1;32(Web Server issue):W108-12.


1-Mb resolution array-based comparative genomic hybridization using a BAC clone set optimized for cancer gene analysis.

Greshock J, Naylor TL, Margolin A, Diskin S, Cleaver SH, Futreal PA, deJong PJ, Zhao S, Liebman M, Weber BL.

Genome Res. 2004 Jan;14(1):179-87.


A functional genomic analysis of cell morphology using RNA interference.

Kiger AA, Baum B, Jones S, Jones MR, Coulson A, Echeverri C, Perrimon N.

J Biol. 2003;2(4):27.


Locating sequence on FPC maps and selecting a minimal tiling path.

Engler FW, Hatfield J, Nelson W, Soderlund CA.

Genome Res. 2003 Sep;13(9):2152-63.


DNannotator: Annotation software tool kit for regional genomic sequences.

Liu C, Bonner TI, Nguyen T, Lyons JL, Christian SL, Gershon ES.

Nucleic Acids Res. 2003 Jul 1;31(13):3729-35.


The microcell mediated transfer of human chromosome 8 into highly metastatic rat liver cancer cell line C5F.

Liu H, Ye SL, Yang J, Tang ZY, Liu YK, Qin LX, Qiu SJ, Sun RX.

World J Gastroenterol. 2003 Mar;9(3):449-53.


Identification of a locus for a form of spondyloepiphyseal dysplasia on chromosome 15q26.1: exclusion of aggrecan as a candidate gene.

Eyre S, Roby P, Wolstencroft K, Spreckley K, Aspinwall R, Bayoumi R, Al-Gazali L, Ramesar R, Beighton P, Wallis G.

J Med Genet. 2002 Sep;39(9):634-8. Erratum in: J Med Genet. 2005 Jun;42(6):e34.


The human genome browser at UCSC.

Kent WJ, Sugnet CW, Furey TS, Roskin KM, Pringle TH, Zahler AM, Haussler D.

Genome Res. 2002 Jun;12(6):996-1006.


Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone.

Laurin N, Brown JP, Morissette J, Raymond V.

Am J Hum Genet. 2002 Jun;70(6):1582-8.


JSNP: a database of common gene variations in the Japanese population.

Hirakawa M, Tanaka T, Hashimoto Y, Kuroda M, Takagi T, Nakamura Y.

Nucleic Acids Res. 2002 Jan 1;30(1):158-62.


The map problem: a comparison of genetic and sequence-based physical maps.

DeWan AT, Parrado AR, Matise TC, Leal SM.

Am J Hum Genet. 2002 Jan;70(1):101-7.


Mouse BAC ends quality assessment and sequence analyses.

Zhao S, Shatsman S, Ayodeji B, Geer K, Tsegaye G, Krol M, Gebregeorgis E, Shvartsbeyn A, Russell D, Overton L, Jiang L, Dimitrov G, Tran K, Shetty J, Malek JA, Feldblyum T, Nierman WC, Fraser CM.

Genome Res. 2001 Oct;11(10):1736-45. Erratum in: Genome Res 2001 Nov;11(11):1968.


The 1.4-Mb CMT1A duplication/HNPP deletion genomic region reveals unique genome architectural features and provides insights into the recent evolution of new genes.

Inoue K, Dewar K, Katsanis N, Reiter LT, Lander ES, Devon KL, Wyman DW, Lupski JR, Birren B.

Genome Res. 2001 Jun;11(6):1018-33.


Human BAC ends.

Zhao S.

Nucleic Acids Res. 2000 Jan 1;28(1):129-32.

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