Related references
Note: Only part of the references are listed.Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma
Ignacio Varela et al.
NATURE (2011)
Targeted resequencing of candidate genes using selector probes
H. Johansson et al.
NUCLEIC ACIDS RESEARCH (2011)
Genomic DNA Pooling Strategy for Next-Generation Sequencing-Based Rare Variant Discovery in Abdominal Aortic Aneurysm Regions of Interest-Challenges and Limitations
Magdalena Harakalova et al.
JOURNAL OF CARDIOVASCULAR TRANSLATIONAL RESEARCH (2011)
A scalable, fully automated process for construction of sequence-ready human exome targeted capture libraries
Sheila Fisher et al.
GENOME BIOLOGY (2011)
Exome Sequencing Identifies WDR35 Variants Involved in Sensenbrenner Syndrome
Christian Gilissen et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2010)
Combining target enrichment with barcode multiplexing for high throughput SNP discovery
Nik Cummings et al.
BMC GENOMICS (2010)
Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing
Jamie K. Teer et al.
GENOME RESEARCH (2010)
Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations
Kaya Bilguvar et al.
NATURE (2010)
A map of human genome variation from population-scale sequencing
David Altshuler et al.
NATURE (2010)
Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome
Peter M. Krawitz et al.
NATURE GENETICS (2010)
Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants
Yingrui Li et al.
NATURE GENETICS (2010)
Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome
Sarah B. Ng et al.
NATURE GENETICS (2010)
A de novo paradigm for mental retardation
Lisenka E. L. M. Vissers et al.
NATURE GENETICS (2010)
Mutation discovery by targeted genomic enrichment of multiplexed barcoded samples
Isaac J. Nijman et al.
NATURE METHODS (2010)
Target-enrichment strategies for next-generation sequencing
Lira Mamanova et al.
NATURE METHODS (2010)
APPLICATIONS OF NEXT-GENERATION SEQUENCING Sequencing technologies - the next generation
Michael L. Metzker
NATURE REVIEWS GENETICS (2010)
Exome Sequencing, ANGPTL3 Mutations, and Familial Combined Hypolipidemia
Kiran Musunuru et al.
NEW ENGLAND JOURNAL OF MEDICINE (2010)
Accurate SNP and mutation detection by targeted custom microarray-based genomic enrichment of short-fragment sequencing libraries
Michal Mokry et al.
NUCLEIC ACIDS RESEARCH (2010)
Frequent Mutation of BAP1 in Metastasizing Uveal Melanomas
J. William Harbour et al.
SCIENCE (2010)
Whole exome capture in solution with 3 Gbp of data
Matthew N. Bainbridge et al.
GENOME BIOLOGY (2010)
Improving the efficiency of genomic loci capture using oligonucleotide arrays for high throughput resequencing
Hane Lee et al.
BMC GENOMICS (2009)
Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing
Andreas Gnirke et al.
NATURE BIOTECHNOLOGY (2009)
Hybrid selection of discrete genomic intervals on custom-designed microarrays for massively parallel sequencing
Emily Hodges et al.
NATURE PROTOCOLS (2009)
The diploid genome sequence of an Asian individual
Jun Wang et al.
NATURE (2008)
Microarray-based genomic selection for high-throughput resequencing
David T. Okou et al.
NATURE METHODS (2007)
Share Paper
