Clinical application of next-generation sequencing for Mendelian diseases

10.1186/s40246-015-0031-5

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Bibliographic Details
Main Authors:	Jamuar, S.S, Tan, E.-C
Other Authors:	DUKE-NUS MEDICAL SCHOOL
Format:	Review
Published:	2020
Subjects:	DNA sequence exome genetic disorder genetic screening genetics high throughput sequencing human medical research mutation procedures Biomedical Research Exome Genetic Diseases, Inborn Genetic Testing High-Throughput Nucleotide Sequencing Humans Mutation Sequence Analysis, DNA
Online Access:	https://scholarbank.nus.edu.sg/handle/10635/183590
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Institution:	National University of Singapore

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spelling	sg-nus-scholar.10635-1835902023-09-21T08:11:59Z Clinical application of next-generation sequencing for Mendelian diseases Jamuar, S.S Tan, E.-C DUKE-NUS MEDICAL SCHOOL INSTITUTE OF MOLECULAR & CELL BIOLOGY DNA sequence exome genetic disorder genetic screening genetics high throughput sequencing human medical research mutation procedures Biomedical Research Exome Genetic Diseases, Inborn Genetic Testing High-Throughput Nucleotide Sequencing Humans Mutation Sequence Analysis, DNA 10.1186/s40246-015-0031-5 Human genomics 9 10 2020-11-17T08:51:25Z 2020-11-17T08:51:25Z 2015 Review Jamuar, S.S, Tan, E.-C (2015). Clinical application of next-generation sequencing for Mendelian diseases. Human genomics 9 : 10. ScholarBank@NUS Repository. https://doi.org/10.1186/s40246-015-0031-5 14797364 https://scholarbank.nus.edu.sg/handle/10635/183590 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ Unpaywall 20201031
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
topic	DNA sequence exome genetic disorder genetic screening genetics high throughput sequencing human medical research mutation procedures Biomedical Research Exome Genetic Diseases, Inborn Genetic Testing High-Throughput Nucleotide Sequencing Humans Mutation Sequence Analysis, DNA
spellingShingle	DNA sequence exome genetic disorder genetic screening genetics high throughput sequencing human medical research mutation procedures Biomedical Research Exome Genetic Diseases, Inborn Genetic Testing High-Throughput Nucleotide Sequencing Humans Mutation Sequence Analysis, DNA Jamuar, S.S Tan, E.-C Clinical application of next-generation sequencing for Mendelian diseases
description	10.1186/s40246-015-0031-5
author2	DUKE-NUS MEDICAL SCHOOL
author_facet	DUKE-NUS MEDICAL SCHOOL Jamuar, S.S Tan, E.-C
format	Review
author	Jamuar, S.S Tan, E.-C
author_sort	Jamuar, S.S
title	Clinical application of next-generation sequencing for Mendelian diseases
title_short	Clinical application of next-generation sequencing for Mendelian diseases
title_full	Clinical application of next-generation sequencing for Mendelian diseases
title_fullStr	Clinical application of next-generation sequencing for Mendelian diseases
title_full_unstemmed	Clinical application of next-generation sequencing for Mendelian diseases
title_sort	clinical application of next-generation sequencing for mendelian diseases
publishDate	2020
url	https://scholarbank.nus.edu.sg/handle/10635/183590
_version_	1779153091723001856

Clinical application of next-generation sequencing for Mendelian diseases

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