Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing

Massively parallel sequencing of ataxia genes after array-based enrichment

(2010) Alexander Hoischen et al.   HUMAN MUTATION

Genetic diagnosis of familial breast cancer using clonal sequencing

(2010) Joanne E. Morgan et al.   HUMAN MUTATION

Target-enrichment strategies for next-generation sequencing

(2010) Lira Mamanova et al.   NATURE METHODS

Individual Genomes on the Horizon

(2010) Richard P. Lifton   NEW ENGLAND JOURNAL OF MEDICINE

Gene Patenting — Is the Pendulum Swinging Back?

(2010) Aaron S. Kesselheim et al.   NEW ENGLAND JOURNAL OF MEDICINE

DNA Sequence Capture and Enrichment by Microarray Followed by Next-Generation Sequencing for Targeted Resequencing: Neurofibromatosis Type 1 Gene as a Model

(2009) L.-S. Chou et al.   CLINICAL CHEMISTRY

Microarray-based multicycle-enrichment of genomic subsets for targeted next-generation sequencing

(2009) D. Summerer et al.   GENOME RESEARCH

Beyond Li Fraumeni Syndrome: Clinical Characteristics of Families Withp53Germline Mutations

(2009) Kelly D. Gonzalez et al.   JOURNAL OF CLINICAL ONCOLOGY

Enrichment of sequencing targets from the human genome by solution hybridization

(2009) Ryan Tewhey et al.   GENOME BIOLOGY

Mapping short DNA sequencing reads and calling variants using mapping quality scores

(2008) H. Li et al.   GENOME RESEARCH

Simultaneous mutation and copy number variation (CNV) detection by multiplex PCR-based GS-FLX sequencing

(2008) Dirk Goossens et al.   HUMAN MUTATION