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.
93 related articles for article (PubMed ID: 8205191)
21. Using the TIGR assembler in shotgun sequencing projects. Pop M; Kosack D Methods Mol Biol; 2004; 255():279-94. PubMed ID: 15020832 [No Abstract] [Full Text] [Related]
22. Improvement of base-calling in multilane automated DNA sequencing by use of electrophoretic calibration standards, data linearization, and trace alignment. Izmailov A; Yager TD; Zaleski H; Darash S Electrophoresis; 2001 Jun; 22(10):1906-14. PubMed ID: 11465487 [TBL] [Abstract][Full Text] [Related]
26. PRIMO: A primer design program that applies base quality statistics for automated large-scale DNA sequencing. Li P; Kupfer KC; Davies CJ; Burbee D; Evans GA; Garner HR Genomics; 1997 Mar; 40(3):476-85. PubMed ID: 9073516 [TBL] [Abstract][Full Text] [Related]
27. A global approach for contig construction. Gleizes A; Hénaut A Comput Appl Biosci; 1994 Jul; 10(4):401-8. PubMed ID: 7804872 [TBL] [Abstract][Full Text] [Related]
28. Using the FASTA program to search protein and DNA sequence databases. Pearson WR Methods Mol Biol; 1994; 24():307-31. PubMed ID: 8205202 [No Abstract] [Full Text] [Related]
32. A greedy algorithm for aligning DNA sequences. Zhang Z; Schwartz S; Wagner L; Miller W J Comput Biol; 2000; 7(1-2):203-14. PubMed ID: 10890397 [TBL] [Abstract][Full Text] [Related]
33. Alignment-free sequence comparison for biologically realistic sequences of moderate length. Burden CJ; Jing J; Wilson SR Stat Appl Genet Mol Biol; 2012; 11(1):Article 3. PubMed ID: 22624182 [TBL] [Abstract][Full Text] [Related]
34. Staden: searching for restriction sites. Staden R Methods Mol Biol; 1994; 25():79-85. PubMed ID: 8004182 [No Abstract] [Full Text] [Related]
35. A dataset generator for whole genome shotgun sequencing. Myers G Proc Int Conf Intell Syst Mol Biol; 1999; ():202-10. PubMed ID: 10786303 [TBL] [Abstract][Full Text] [Related]
36. Pro-Frame: similarity-based gene recognition in eukaryotic DNA sequences with errors. Mironov AA; Novichkov PS; Gelfand MS Bioinformatics; 2001 Jan; 17(1):13-5. PubMed ID: 11222258 [TBL] [Abstract][Full Text] [Related]
37. EST_GENOME: a program to align spliced DNA sequences to unspliced genomic DNA. Mott R Comput Appl Biosci; 1997 Aug; 13(4):477-8. PubMed ID: 9283765 [No Abstract] [Full Text] [Related]
38. MSA-PAD: DNA multiple sequence alignment framework based on PFAM accessed domain information. Balech B; Vicario S; Donvito G; Monaco A; Notarangelo P; Pesole G Bioinformatics; 2015 Aug; 31(15):2571-3. PubMed ID: 25819080 [TBL] [Abstract][Full Text] [Related]
39. Shotgun sequencing of the human genome. Venter JC; Adams MD; Sutton GG; Kerlavage AR; Smith HO; Hunkapiller M Science; 1998 Jun; 280(5369):1540-2. PubMed ID: 9644018 [No Abstract] [Full Text] [Related]
40. Sequence assembly and finishing methods. Staden R; Judge DP; Bonfield JK Methods Biochem Anal; 2001; 43():303-22. PubMed ID: 11449730 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]