Genetic variation in an individual human exome

10.1371/journal.pgen.1000160

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Main Authors: 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.
Other Authors: MEDICINE
Format: Article
Published: 2019
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Online Access:https://scholarbank.nus.edu.sg/handle/10635/161684
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spelling 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
institution National University of Singapore
building NUS Library
continent Asia
country Singapore
Singapore
content_provider NUS Library
collection ScholarBank@NUS
topic 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)
spellingShingle 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
description 10.1371/journal.pgen.1000160
author2 MEDICINE
author_facet 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.
format 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.
author_sort 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
title_sort genetic variation in an individual human exome
publishDate 2019
url https://scholarbank.nus.edu.sg/handle/10635/161684
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