Genetic variation in an individual human exome
10.1371/journal.pgen.1000160
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sg-nus-scholar.10635-1616842024-04-24T05:54:18Z Genetic variation in an individual human exome Ng P.C. Levy S. Huang J. Stockwell T.B. Walenz B.P. Li K. Axelrod N. Busam D.A. Strausberg R.L. Venter J.C. MEDICINE amino acid protein article bioinformatics exon gene gene deletion gene insertion genetic variability genome genomics human protein function single nucleotide polymorphism comparative study gene frequency genetic disorder genetics male metabolism mutation phenotype single nucleotide polymorphism Exons Gene Frequency Genetic Diseases, Inborn Genome, Human Humans Male Mutation Phenotype Polymorphism, Single Nucleotide Proteins Variation (Genetics) 10.1371/journal.pgen.1000160 PLoS Genetics 4 8 e1000160 2019-11-06T09:37:34Z 2019-11-06T09:37:34Z 2008 Article Ng P.C., Levy S., Huang J., Stockwell T.B., Walenz B.P., Li K., Axelrod N., Busam D.A., Strausberg R.L., Venter J.C. (2008). Genetic variation in an individual human exome. PLoS Genetics 4 (8) : e1000160. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pgen.1000160 15537390 https://scholarbank.nus.edu.sg/handle/10635/161684 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ Unpaywall 20191101 |
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amino acid protein article bioinformatics exon gene gene deletion gene insertion genetic variability genome genomics human protein function single nucleotide polymorphism comparative study gene frequency genetic disorder genetics male metabolism mutation phenotype single nucleotide polymorphism Exons Gene Frequency Genetic Diseases, Inborn Genome, Human Humans Male Mutation Phenotype Polymorphism, Single Nucleotide Proteins Variation (Genetics) |
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amino acid protein article bioinformatics exon gene gene deletion gene insertion genetic variability genome genomics human protein function single nucleotide polymorphism comparative study gene frequency genetic disorder genetics male metabolism mutation phenotype single nucleotide polymorphism Exons Gene Frequency Genetic Diseases, Inborn Genome, Human Humans Male Mutation Phenotype Polymorphism, Single Nucleotide Proteins Variation (Genetics) Ng P.C. Levy S. Huang J. Stockwell T.B. Walenz B.P. Li K. Axelrod N. Busam D.A. Strausberg R.L. Venter J.C. Genetic variation in an individual human exome |
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10.1371/journal.pgen.1000160 |
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MEDICINE |
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MEDICINE Ng P.C. Levy S. Huang J. Stockwell T.B. Walenz B.P. Li K. Axelrod N. Busam D.A. Strausberg R.L. Venter J.C. |
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Article |
author |
Ng P.C. Levy S. Huang J. Stockwell T.B. Walenz B.P. Li K. Axelrod N. Busam D.A. Strausberg R.L. Venter J.C. |
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Ng P.C. |
title |
Genetic variation in an individual human exome |
title_short |
Genetic variation in an individual human exome |
title_full |
Genetic variation in an individual human exome |
title_fullStr |
Genetic variation in an individual human exome |
title_full_unstemmed |
Genetic variation in an individual human exome |
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genetic variation in an individual human exome |
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2019 |
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https://scholarbank.nus.edu.sg/handle/10635/161684 |
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