REPuter: the manifold applications of repeat analysis on a genomic scale.
暂无分享,去创建一个
J. Stoye | S. Kurtz | R. Giegerich | E. Ohlebusch | J. V. Choudhuri | C. Schleiermacher | Enno Ohlebusch
[1] Michael J. Fischer,et al. The String-to-String Correction Problem , 1974, JACM.
[2] Robert E. Tarjan,et al. Fast Algorithms for Finding Nearest Common Ancestors , 1984, SIAM J. Comput..
[3] Esko Ukkonen,et al. Algorithms for Approximate String Matching , 1985, Inf. Control..
[4] Uzi Vishkin,et al. On Finding Lowest Common Ancestors: Simplification and Parallelization , 1988, AWOC.
[5] A. Kerlavage,et al. Complementary DNA sequencing: expressed sequence tags and human genome project , 1991, Science.
[6] R. Durbin,et al. A dot-matrix program with dynamic threshold control suited for genomic DNA and protein sequence analysis. , 1995, Gene.
[7] Dan Gusfield,et al. Algorithms on Strings, Trees, and Sequences - Computer Science and Computational Biology , 1997 .
[8] S. Karlin,et al. Prediction of complete gene structures in human genomic DNA. , 1997, Journal of molecular biology.
[9] N. W. Davis,et al. The complete genome sequence of Escherichia coli K-12. , 1997, Science.
[10] Eugene W. Myers,et al. Estimating the Probability of Approximate Matches , 1997, CPM.
[11] Carton W. Chen,et al. The telomeres of Streptomyces chromosomes contain conserved palindromic sequences with potential to form complex secondary structures , 1998, Molecular microbiology.
[12] A brief guide to phylogenetic software. , 1998, Trends in genetics : TIG.
[13] Alex van Belkum,et al. Short-Sequence DNA Repeats in Prokaryotic Genomes , 1998, Microbiology and Molecular Biology Reviews.
[14] S Holloway,et al. A chromosomal deletion map of human malformations. , 1998, American journal of human genetics.
[15] B. Morrow,et al. Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome. , 1999, American journal of human genetics.
[16] Stefan Kurtz,et al. Reducing the space requirement of suffix trees , 1999, Softw. Pract. Exp..
[17] S. Salzberg,et al. Alignment of whole genomes. , 1999, Nucleic acids research.
[18] G. Benson,et al. Tandem repeats finder: a program to analyze DNA sequences. , 1999, Nucleic acids research.
[19] Stefan Kurtz,et al. REPuter: fast computation of maximal repeats in complete genomes , 1999, Bioinform..
[20] Karl Popper,et al. The REPRO server : finding protein internal sequence repeats through the Web , 2000 .
[21] D. Womble,et al. GCG: The Wisconsin Package of sequence analysis programs. , 2000, Methods in molecular biology.
[22] Enno Ohlebusch,et al. Computation and Visualization of Degenerate Repeats in Complete Genomes , 2000, ISMB.
[23] B. Roe,et al. Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis. , 2000, Human molecular genetics.
[24] I. Longden,et al. EMBOSS: the European Molecular Biology Open Software Suite. , 2000, Trends in genetics : TIG.
[25] International Human Genome Sequencing Consortium. Initial sequencing and analysis of the human genome , 2001, Nature.