Impact of next generation sequencing: The 2009 human genome variation society scientific meeting

Human Mutation

Volumn 31, Issue 4, 2010, Pages 500-503

  Oetting, William S ^a  

^a UNIVERSITY OF MINNESOTA   (United States)

Author keywords

Databases; HGVS; Meeting report; Mutations; Next generation sequencing; Variation

Indexed keywords

COMPARATIVE GENOMIC HYBRIDIZATION; CONFERENCE PAPER; GENE MUTATION; GENE SEQUENCE; GENE TECHNOLOGY; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC VARIABILITY; HUMAN; PRIORITY JOURNAL;

DISEASE; GENETIC VARIATION; GENOME, HUMAN; GENOMICS; HUMANS; SEQUENCE ANALYSIS, DNA; SOCIETIES, SCIENTIFIC;

EID: 77950403729     PISSN: 10597794     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.21210     Document Type: Conference Paper

References (2)

1. Desmet FO, Hamroun D, Lalande M, Collod-Beroud G, Claustres M, Beroud C. 2009. Human Splicing Finder: an online bioinformatics toolto predict splicing signals. Nucleic Acids Res 37:e67.
2. Frederic MY, Lalande M, Boileau C, Hamroun D, Claustres M, Beroud C, Collod-Beroud G. 2009. UMD-predictor, a new prediction toolfor nucleotide substitution pathogenicity - application to four genes: FBN1, FBN2, TGFBR1, and TGFBR2. Hum Mutat 30:952-959.