Progress in detecting genetic alterations and their association with human disease

Journal of Molecular Biology

Volumn 425, Issue 21, 2013, Pages 3914-3918

  Schwartz, Charles E ^a   Chen, Chin Fu ^a  

^a GREENWOOD GENETIC CENTER   (United States)

Author keywords

bioinformatics; gene prioritization; next generation sequencing; whole exome sequencing

Indexed keywords

AMINO ACID; MESSENGER RNA; NUCLEOTIDE;

ALGORITHM; AMINO ACID SEQUENCE; ARTIFICIAL NEURAL NETWORK; CONSENSUS SEQUENCE; DISEASES; ENTROPY; EXOME; FOLLOW UP; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC CONSERVATION; HUMAN; HUMAN GENOME; INDEL MUTATION; MUTATION; PATIENT; PHENOTYPE; PREDICTION; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN PROTEIN INTERACTION; PROTEIN STABILITY; REVIEW; SUPPORT VECTOR MACHINE;

BIOINFORMATICS; GENE PRIORITIZATION; NEXT GENERATION SEQUENCING; NGS; SUPPORT VECTOR MACHINE; SVM; WHOLE EXOME SEQUENCING;

ANIMALS; EXOME; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; GENOME, HUMAN; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; MUTATION; SEQUENCE ANALYSIS, DNA;

EID: 84885189078     PISSN: 00222836     EISSN: 10898638     Source Type: Journal    
DOI: 10.1016/j.jmb.2013.07.023     Document Type: Review

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