BAC finishing strategies.

[1]  C. Desmarais,et al.  Automated finishing with autofinish. , 2001, Genome research.

[2]  André Goffeau,et al.  The yeast genome directory. , 1997, Nature.

[3]  J. Mullikin,et al.  Sequencing the Genome, Fast , 1999, Science.

[4]  P. Richterich,et al.  Estimation of errors in "raw" DNA sequences: a validation study. , 1998, Genome research.

[5]  S. Pääbo,et al.  Improved cycle sequencing of GC-rich templates by a combination of nucleotide analogs. , 2000, BioTechniques.

[6]  Andrew Smith.  Genome sequence of the nematode C-elegans: A platform for investigating biology , 1998 .

[7]  H. Griffin,et al.  Computer analysis of sequence data. , 1994, Methods in molecular biology.

[8]  P. D. de Jong,et al.  A bacterial artificial chromosome library for sequencing the complete human genome. , 2001, Genome research.

[9]  R. Staden,et al.  An oligo-screening strategy to fill gaps found during shotgun sequencing projects. , 1998, DNA sequence : the journal of DNA sequencing and mapping.

[10]  D. Haussler,et al.  A physical map of the human genome , 2001, Nature.

[11]  K Watanabe,et al.  Extraordinarily stable mini-hairpins: electrophoretical and thermal properties of the various sequence variants of d(GCGAAAGC) and their effect on DNA sequencing. , 1992, Nucleic acids research.

[12]  The Arabidopsis Genome Initiative.  Analysis of the genome sequence of the flowering plant Arabidopsis thaliana , 2000, Nature.

[13]  P. Green,et al.  Base-calling of automated sequencer traces using phred. I. Accuracy assessment. , 1998, Genome research.

[14]  J. V. Moran,et al.  Initial sequencing and analysis of the human genome. , 2001, Nature.

[15]  J E Sulston,et al.  Short-insert libraries as a method of problem solving in genome sequencing. , 1998, Genome research.

[16]  P Green,et al.  Base-calling of automated sequencer traces using phred. II. Error probabilities. , 1998, Genome research.

[17]  P. Green,et al.  Consed: a graphical tool for sequence finishing. , 1998, Genome research.