Prediction of nonsynonymous single nucleotide polymorphisms in human disease-associated genes

[1]  P Bork,et al.  Individual variation in protein-coding sequences of human genome. , 2000, Advances in protein chemistry.

[2]  N. Shen,et al.  Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis , 1999, Nature Genetics.

[3]  L. Kruglyak Prospects for whole-genome linkage disequilibrium mapping of common disease genes , 1999, Nature Genetics.

[4]  Michael N. Edmonson,et al.  Reliable identification of large numbers of candidate SNPs from public EST data , 1999, Nature Genetics.

[5]  T. Ideker,et al.  Mining SNPs from EST databases. , 1999, Genome research.

[6]  E. Lander,et al.  Characterization of single-nucleotide polymorphisms in coding regions of human genes , 1999 .

[7]  E Lai,et al.  A 4-Mb high-density single nucleotide polymorphism-based map around human APOE. , 1998, Genomics.

[8]  F. Collins,et al.  New goals for the U.S. Human Genome Project: 1998-2003. , 1998, Science.

[9]  E. Vesell,et al.  Genetic Variation as a Guide to Drug Development , 1998, Science.

[10]  P. Kwok,et al.  Overlapping genomic sequences: a treasure trove of single-nucleotide polymorphisms. , 1998, Genome research.

[11]  C. Nusbaum,et al.  Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome. , 1998, Science.

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

[13]  Francis S. Collins,et al.  Variations on a Theme: Cataloging Human DNA Sequence Variation , 1997, Science.

[14]  O. Ohara,et al.  A DNA cycle sequencing reaction that minimizes compressions on automated fluorescent sequencers. , 1997, Nucleic acids research.

[15]  F. Ledley,et al.  Mutations in mut methylmalonic acidemia: Clinical and enzymatic correlations , 1997, Human mutation.

[16]  C. Auffray,et al.  The I.M.A.G.E. Consortium: an integrated molecular analysis of genomes and their expression. , 1996, Genomics.

[17]  T. Saheki,et al.  Mutations in argininosuccinate synthetase mRNA in Japanese patients, causing classical citrullinemia. , 1994, American journal of human genetics.

[18]  M. Soares,et al.  Construction and characterization of a normalized cDNA library. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[19]  V. Solovyev,et al.  Assignment of position-specific error probability to primary DNA sequence data. , 1994, Nucleic acids research.

[20]  G. Hartzell,et al.  DNA sequence confidence estimation. , 1994, Genomics.

[21]  A. Bairoch,et al.  The SWISS-PROT protein sequence data bank. , 1991, Nucleic acids research.