Making good use of exorne sequencing;Du bon usage des exornes

Medecine/Sciences

Volumn 26, Issue 12, 2010, Pages 1111-1113

  Jordan, Bertrand ^a  

^a Parc Scientifique de Luminy   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ANGIOPOIETIN; ANGPTL3 PROTEIN, HUMAN; ANGPTL3 PROTEIN, MOUSE; APOLIPOPROTEIN B; LOW DENSITY LIPOPROTEIN CHOLESTEROL; TRIACYLGLYCEROL;

ADULT; ANIMAL; ARTICLE; BLOOD; CHILD; DNA SEQUENCE; DYSLIPIDEMIA; ECONOMICS; EXON; FEMALE; GENETIC ASSOCIATION; GENETICS; GENOTYPE; HUMAN; LIVER; MALE; METABOLISM; MOUSE; PEDIGREE; STOP CODON;

ADULT; ANGIOPOIETINS; ANIMALS; APOLIPOPROTEINS B; CHILD; CHOLESTEROL, LDL; CODON, NONSENSE; DYSLIPIDEMIAS; EXONS; FEMALE; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HUMANS; LIVER; MALE; MICE; PEDIGREE; SEQUENCE ANALYSIS, DNA; TRIGLYCERIDES;

EID: 78651389128     PISSN: 07670974     EISSN: None     Source Type: Journal    
DOI: 10.1051/medsci/201026121111     Document Type: Article

References (8)

1. Manolio TA, Collins FS, Cox NJ, et al. Finding the missing heritability of complex diseases. Nature 2009 ; 461: 747-53.
2. Jordan B. À la recherche de l'héritabilité perdue. Med Sci (Paris) 2010 ; 26 : 541-3.
3. Jordan B. Séquence : Ie juste prix... Med Sci (Paris) 2009 ; 25 : 988-9.
4. 1000 genomes project consortium, Durbin RM, Abecasis GR, Altshuler DL, et al. A map of human genome variation from population-scale sequencing. Nature 2010 ; 467:1061-73.
5. Maher B. Exorne sequencing takes centre stage in cancer profiling. Nature 2009 ; 459:146-7.
6. Musunuru K, Pirruccello JP, Do R, et al. Exorne sequencing, ANGPTL3 mutations, and familial combined hypolipidemic. N Engl J Med 2010 ; 363 : 2220-7.
7. Gnirke A, Melnikov A, Maguire J, et al. Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing. Nat Biotechnol 2009 ; 27:182-9.
8. Pleasance ED, Cheetham RK, Stephens PJ, et al. A comprehensive catalogue of somatic mutations from a human cancer genome. Nature 2010 ; 463 : 191-6.