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Items: 15


Microarrays and RNA-Seq identify molecular mechanisms driving the end of nephron production.

Brunskill EW, Lai HL, Jamison DC, Potter SS, Patterson LT.

BMC Dev Biol. 2011 Mar 12;11:15. doi: 10.1186/1471-213X-11-15.


Ontogenomic study of the relationship between number of gene splice variants and GO categorization.

Kahn AB, Zeeberg BR, Ryan MC, Jamison DC, Rockoff DM, Pommier Y, Weinstein JN.

Bioinformatics. 2010 Aug 15;26(16):1945-9. doi: 10.1093/bioinformatics/btq335. Epub 2010 Jul 8.


Structured Query Language (SQL) fundamentals.

Jamison DC.

Curr Protoc Bioinformatics. 2003 Feb;Chapter 9:Unit9.2. doi: 10.1002/0471250953.bi0902s00.


The EDGE hypothesis: epigenetically directed genetic errors in repeat-containing proteins (RCPs) involved in evolution, neuroendocrine signaling, and cancer.

Ruden DM, Jamison DC, Zeeberg BR, Garfinkel MD, Weinstein JN, Rasouli P, Lu X.

Front Neuroendocrinol. 2008 Jun;29(3):428-44. doi: 10.1016/j.yfrne.2007.12.004. Epub 2008 Jan 8. Review.


Statistical geometry based prediction of nonsynonymous SNP functional effects using random forest and neuro-fuzzy classifiers.

Barenboim M, Masso M, Vaisman II, Jamison DC.

Proteins. 2008 Jun;71(4):1930-9. doi: 10.1002/prot.21838.


SpliceMiner: a high-throughput database implementation of the NCBI Evidence Viewer for microarray splice variant analysis.

Kahn AB, Ryan MC, Liu H, Zeeberg BR, Jamison DC, Weinstein JN.

BMC Bioinformatics. 2007 Mar 5;8:75.


The distribution of SNPs in human gene regulatory regions.

Guo Y, Jamison DC.

BMC Genomics. 2005 Oct 6;6:140.


Statistical geometry approach to the study of functional effects of human nonsynonymous SNPs.

Barenboim M, Jamison DC, Vaisman II.

Hum Mutat. 2005 Nov;26(5):471-6.


Online analytical processing (OLAP): a fast and effective data mining tool for gene expression databases.

Alkharouf NW, Jamison DC, Matthews BF.

J Biomed Biotechnol. 2005 Jun 30;2005(2):181-8.


Open bioinformatics.

Jamison DC.

Bioinformatics. 2003 Apr 12;19(6):679-80. No abstract available.


ComboScreen facilitates the multiplex hybridization-based screening of high-density clone arrays.

Jamison DC, Thomas JW, Green ED.

Bioinformatics. 2000 Aug;16(8):678-84.


The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder.

Lai CS, Fisher SE, Hurst JA, Levy ER, Hodgson S, Fox M, Jeremiah S, Povey S, Jamison DC, Green ED, Vargha-Khadem F, Monaco AP.

Am J Hum Genet. 2000 Aug;67(2):357-68. Epub 2000 Jul 5.


Comparative genome mapping in the sequence-based era: early experience with human chromosome 7.

Thomas JW, Summers TJ, Lee-Lin SQ, Maduro VV, Idol JR, Mastrian SD, Ryan JF, Jamison DC, Green ED.

Genome Res. 2000 May;10(5):624-33. Review.


Comparative genomic sequence analysis of the human and mouse cystic fibrosis transmembrane conductance regulator genes.

Ellsworth RE, Jamison DC, Touchman JW, Chissoe SL, Braden Maduro VV, Bouffard GG, Dietrich NL, Beckstrom-Sternberg SM, Iyer LM, Weintraub LA, Cotton M, Courtney L, Edwards J, Maupin R, Ozersky P, Rohlfing T, Wohldmann P, Miner T, Kemp K, Kramer J, Korf I, Pepin K, Antonacci-Fulton L, Fulton RS, Minx P, Hillier LW, Wilson RK, Waterston RH, Miller W, Green ED.

Proc Natl Acad Sci U S A. 2000 Feb 1;97(3):1172-7.


An extensible network query unification system for biological databases.

Jamison DC, Mills B, Schatz B.

Comput Appl Biosci. 1996 Apr;12(2):145-50.

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