These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
520 related items for PubMed ID: 20804568
1. The missing graphical user interface for genomics. Schatz MC. Genome Biol; 2010; 11(8):128. PubMed ID: 20804568 [Abstract] [Full Text] [Related]
2. Galactic Circos: User-friendly Circos plots within the Galaxy platform. Rasche H, Hiltemann S. Gigascience; 2020 Jun 01; 9(6):. PubMed ID: 32530465 [Abstract] [Full Text] [Related]
3. PanWeb: A web interface for pan-genomic analysis. Pantoja Y, Pinheiro K, Veras A, Araújo F, Lopes de Sousa A, Guimarães LC, Silva A, Ramos RTJ. PLoS One; 2017 Jun 01; 12(5):e0178154. PubMed ID: 28542514 [Abstract] [Full Text] [Related]
9. DolphinNext: a distributed data processing platform for high throughput genomics. Yukselen O, Turkyilmaz O, Ozturk AR, Garber M, Kucukural A. BMC Genomics; 2020 Apr 19; 21(1):310. PubMed ID: 32306927 [Abstract] [Full Text] [Related]
10. G-OnRamp: Generating genome browsers to facilitate undergraduate-driven collaborative genome annotation. Sargent L, Liu Y, Leung W, Mortimer NT, Lopatto D, Goecks J, Elgin SCR. PLoS Comput Biol; 2020 Jun 19; 16(6):e1007863. PubMed ID: 32497138 [Abstract] [Full Text] [Related]
14. Sequence database versioning for command line and Galaxy bioinformatics servers. Dooley DM, Petkau AJ, Van Domselaar G, Hsiao WW. Bioinformatics; 2016 Apr 15; 32(8):1275-7. PubMed ID: 26656932 [Abstract] [Full Text] [Related]
15. Osiris: accessible and reproducible phylogenetic and phylogenomic analyses within the Galaxy workflow management system. Oakley TH, Alexandrou MA, Ngo R, Pankey MS, Churchill CK, Chen W, Lopker KB. BMC Bioinformatics; 2014 Jul 02; 15():230. PubMed ID: 24990571 [Abstract] [Full Text] [Related]
16. The Galaxy platform for accessible, reproducible and collaborative biomedical analyses: 2016 update. Afgan E, Baker D, van den Beek M, Blankenberg D, Bouvier D, Čech M, Chilton J, Clements D, Coraor N, Eberhard C, Grüning B, Guerler A, Hillman-Jackson J, Von Kuster G, Rasche E, Soranzo N, Turaga N, Taylor J, Nekrutenko A, Goecks J. Nucleic Acids Res; 2016 Jul 08; 44(W1):W3-W10. PubMed ID: 27137889 [Abstract] [Full Text] [Related]
17. CGHPRO -- a comprehensive data analysis tool for array CGH. Chen W, Erdogan F, Ropers HH, Lenzner S, Ullmann R. BMC Bioinformatics; 2005 Apr 05; 6():85. PubMed ID: 15807904 [Abstract] [Full Text] [Related]
18. arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays. Menten B, Pattyn F, De Preter K, Robbrecht P, Michels E, Buysse K, Mortier G, De Paepe A, van Vooren S, Vermeesch J, Moreau Y, De Moor B, Vermeulen S, Speleman F, Vandesompele J. BMC Bioinformatics; 2005 May 23; 6():124. PubMed ID: 15910681 [Abstract] [Full Text] [Related]
19. ballaxy: web services for structural bioinformatics. Hildebrandt AK, Stöckel D, Fischer NM, de la Garza L, Krüger J, Nickels S, Röttig M, Schärfe C, Schumann M, Thiel P, Lenhof HP, Kohlbacher O, Hildebrandt A. Bioinformatics; 2015 Jan 01; 31(1):121-2. PubMed ID: 25183489 [Abstract] [Full Text] [Related]
20. CREDO: a web-based tool for computational detection of conserved sequence motifs in noncoding sequences. Hindemitt T, Mayer KF. Bioinformatics; 2005 Dec 01; 21(23):4304-6. PubMed ID: 16204349 [Abstract] [Full Text] [Related] Page: [Next] [New Search]