A beginners guide to SNP calling from high-Throughput DNA-sequencing data

Human Genetics

Volumn 131, Issue 10, 2012, Pages 1541-1554

  Altmann, André ^a,b   Weber, Peter ^a   Bader, Daniel ^a   Preuß, Michael ^c   Binder, Elisabeth B ^a   Müller Myhsok, Bertram ^a  

^a MAX PLANCK INSTITUTE OF PSYCHIATRY   (Germany)

^b STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF LÜBECK   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CALIBRATION; DNA SEQUENCE; GENE MAPPING; GENETIC VARIABILITY; GENOME ANALYSIS; HIGH THROUGHPUT SEQUENCING; HUMAN; PRIORITY JOURNAL; QUALITY CONTROL; REVIEW; SCORING SYSTEM; SEQUENCE ALIGNMENT; SINGLE NUCLEOTIDE POLYMORPHISM;

COMPUTATIONAL BIOLOGY; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE ANALYSIS, DNA; SOFTWARE;

EID: 84866742932     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/s00439-012-1213-z     Document Type: Review

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