Next Generation Sequencing Data Analysis in Primary Immunodeficiency Disorders – Future Directions

Journal of Clinical Immunology

Volumn 36, Issue , 2016, Pages 68-75

  Fang, Mingyan ^a,b   Abolhassani, Hassan ^a,c   Lim, Che Kang ^a,d   Zhang, Jianguo ^b   Hammarström, Lennart ^a  

^a KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^b BGI SHENZHEN   (China)

^c TEHRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^d SINGAPORE GENERAL HOSPITAL   (Singapore)

Author keywords

candidate gene screening; next generation sequencing; Primary immunodeficiency (PIDs)

Indexed keywords

ARTICLE; COMPARATIVE STUDY; DATA ANALYSIS; GENE IDENTIFICATION; GENE MUTATION; GENETIC ANALYSIS; GENETIC SCREENING; GENETIC VARIABILITY; HUMAN; IMMUNE DEFICIENCY; MODIFIER GENE; MOLECULAR DIAGNOSIS; NEXT GENERATION SEQUENCING; PHENOTYPE; POPULATION STRUCTURE; PREDICTION; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; ALLELE; BIOLOGY; GENETIC ASSOCIATION STUDY; GENETIC PREDISPOSITION; GENETICS; GENOME-WIDE ASSOCIATION STUDY; GENOMICS; GENOTYPE; HIGH THROUGHPUT SEQUENCING; IMMUNOLOGY; MUTATION; PROCEDURES;

ALLELES; COMPUTATIONAL BIOLOGY; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENETIC TESTING; GENOME-WIDE ASSOCIATION STUDY; GENOMICS; GENOTYPE; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; MUTATION;

EID: 84961205601     PISSN: 02719142     EISSN: 15732592     Source Type: Journal    
DOI: 10.1007/s10875-016-0260-y     Document Type: Article

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