Prediction of nonsynonymous single nucleotide polymorphisms in human disease-associated genes
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P. Bork | J. Reich | J. Hanke | I. Zastrow | S. Sunyaev | U. Wirkner | A. Aydın | Inga Zastrow
[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.