New DNA sequencing technologies open a promising era for cancer research and treatment

Clinical and Translational Oncology

Volumn 13, Issue 5, 2011, Pages 301-306

  Sastre, Leandro ^a  

^a HOSPITAL UNIVERSITARIO LA PAZ IDIPAZ   (Spain)

Author keywords

Deep sequencing; Genomic rearrangements; Next generation sequencing; Nucleotide variation; Second generation sequencing; Transcriptome

Indexed keywords

DNA FRAGMENT; MESSENGER RNA;

AMPLICON; CANCER DIAGNOSIS; CANCER GENETICS; CANCER RESEARCH; CANCER RISK; CANCER SUSCEPTIBILITY; CANCER THERAPY; COPY NUMBER VARIATION; DNA SEQUENCE; GENE MUTATION; HUMAN; HUMAN GENOME; MICROSATELLITE INSTABILITY; NUCLEIC ACID BASE SUBSTITUTION; NUCLEOTIDE SEQUENCE; PHARMACOGENOMICS; PROGNOSIS; REVIEW; RNA SEQUENCE; SINGLE NUCLEOTIDE POLYMORPHISM;

CELL LINE, TUMOR; GENETIC PREDISPOSITION TO DISEASE; GENETIC TECHNIQUES; GENOME, HUMAN; GENOMICS; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; MEDICAL ONCOLOGY; MUTATION; NEOPLASMS; PHARMACOGENETICS; SEQUENCE ANALYSIS, DNA;

EID: 79960687447     PISSN: 1699048X     EISSN: 16993055     Source Type: Journal    
DOI: 10.1007/s12094-011-0658-1     Document Type: Review

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