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Sondheimer, NealPerson Why?
ChIP-seq: using high-throughput sequencing to discover protein-DNA interactions.Academic Article Why?
Characterization of Eukaryotic Microbiome Using 18S Amplicon Sequencing.Academic Article Why?
Detecting Alu insertions from high-throughput sequencing data.Academic Article Why?
Reflections on the cost of "low-cost" whole genome sequencing: framing the health policy debate.Academic Article Why?
Detecting copy number variation with mated short reads.Academic Article Why?
Phenotypic and genotypic spectrum of congenital disorders of glycosylation type I and type II.Academic Article Why?
IDBA-MT: de novo assembler for metatranscriptomic data generated from next-generation sequencing technology.Academic Article Why?
Testing personalized medicine: patient and physician expectations of next-generation genomic sequencing in late-stage cancer care.Academic Article Why?
The missing indels: an estimate of indel variation in a human genome and analysis of factors that impede detection.Academic Article Why?
Brudno, MichaelPerson Why?
Identification of a novel MSH6 germline variant in a family with multiple gastro-intestinal malignancies by next generation sequencing.Academic Article Why?
PRISM: pair-read informed split-read mapping for base-pair level detection of insertion, deletion and structural variants.Academic Article Why?
Performance of high-throughput sequencing for the discovery of genetic variation across the complete size spectrum.Academic Article Why?
Genetic Diagnostic Testing for Inherited Cardiomyopathies: Considerations for Offering Multi-Gene Tests in a Health Care Setting.Academic Article Why?
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