DNA sequencing methods in human genetics and disease research

F1000Prime Reports

Volumn 5, Issue , 2013, Pages

  Lehrach, Hans ^a,b,c  

^a MAX PLANCK INSTITUTE FOR MOLECULAR GENETICS   (Germany)

^b Dahlem Centre for Genome Research and Medical Systems Biology   (Germany)

^c ALACRIS THERANOSTICS GMBH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

DNA FRAGMENT; MESSENGER RNA; RIBOSOME RNA;

ALTERNATIVE RNA SPLICING; ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; COPY NUMBER VARIATION; DNA METHYLATION; DNA MODIFICATION; DNA SEQUENCE; FAMILY SIZE; GENOTYPE PHENOTYPE CORRELATION; HAPLOTYPE; HAPLOTYPE MAP; HIGH THROUGHPUT SEQUENCING; HUMAN; HUMAN GENETICS; HUMAN GENOME; HUMAN GENOME PROJECT; MEDICAL RESEARCH; METAGENOME; NUCLEIC ACID ANALYSIS; PERSONALIZED MEDICINE; PROTEIN MODIFICATION; PROTEIN PROTEIN INTERACTION; REVERSE TRANSCRIPTION; RNA SEQUENCE; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 84885652613     PISSN: None     EISSN: 20517599     Source Type: Journal    
DOI: 10.12703/P5-34     Document Type: Article

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