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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2009 | 1 |
2010 | 1 |
2011 | 1 |
2014 | 2 |
2015 | 3 |
2024 | 0 |
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7 results
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Page 1
miRNA Nomenclature: A View Incorporating Genetic Origins, Biosynthetic Pathways, and Sequence Variants.
Trends Genet. 2015 Nov;31(11):613-626. doi: 10.1016/j.tig.2015.09.002. Epub 2015 Oct 8.
Trends Genet. 2015.
PMID: 26453491
Free PMC article.
Review.
GFVO: the Genomic Feature and Variation Ontology.
Baran J, Durgahee BS, Eilbeck K, Antezana E, Hoehndorf R, Dumontier M.
Baran J, et al.
PeerJ. 2015 May 5;3:e933. doi: 10.7717/peerj.933. eCollection 2015.
PeerJ. 2015.
PMID: 26019997
Free PMC article.
Item in Clipboard
Evolution of the Sequence Ontology terms and relationships.
Mungall CJ, Batchelor C, Eilbeck K.
Mungall CJ, et al.
J Biomed Inform. 2011 Feb;44(1):87-93. doi: 10.1016/j.jbi.2010.03.002. Epub 2010 Mar 10.
J Biomed Inform. 2011.
PMID: 20226267
Free PMC article.
Item in Clipboard
Improving the Sequence Ontology terminology for genomic variant annotation.
Cunningham F, Moore B, Ruiz-Schultz N, Ritchie GR, Eilbeck K.
Cunningham F, et al.
J Biomed Semantics. 2015 Jul 31;6:32. doi: 10.1186/s13326-015-0030-4. eCollection 2015.
J Biomed Semantics. 2015.
PMID: 26229585
Free PMC article.
Item in Clipboard
Quantitative measures for the management and comparison of annotated genomes.
Eilbeck K, Moore B, Holt C, Yandell M.
Eilbeck K, et al.
BMC Bioinformatics. 2009 Feb 23;10:67. doi: 10.1186/1471-2105-10-67.
BMC Bioinformatics. 2009.
PMID: 19236712
Free PMC article.
Item in Clipboard
Phevor combines multiple biomedical ontologies for accurate identification of disease-causing alleles in single individuals and small nuclear families.
Singleton MV, Guthery SL, Voelkerding KV, Chen K, Kennedy B, Margraf RL, Durtschi J, Eilbeck K, Reese MG, Jorde LB, Huff CD, Yandell M.
Singleton MV, et al.
Am J Hum Genet. 2014 Apr 3;94(4):599-610. doi: 10.1016/j.ajhg.2014.03.010.
Am J Hum Genet. 2014.
PMID: 24702956
Free PMC article.
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A proposed clinical decision support architecture capable of supporting whole genome sequence information.
Welch BM, Loya SR, Eilbeck K, Kawamoto K.
Welch BM, et al.
J Pers Med. 2014 Apr 4;4(2):176-99. doi: 10.3390/jpm4020176.
J Pers Med. 2014.
PMID: 25411644
Free PMC article.
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