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Nick Sampas
Institution:
Agilent Technologies (United States)
Observed institutions:
Hewlett-Packard (United States),
Agilent Technologies (United States),
National Human Genome Research Institute
OpenAlex ID:
A5110074571
Mapping and sequencing of structural variation from eight human genomes
2008
·
Jeffrey M. Kidd
, Gregory M. Cooper
, et al.
·
Nature
·
1,117
Diversity of Human Copy Number Variation and Multicopy Genes
2010
·
Peter H. Sudmant
, Jacob O. Kitzman
, et al.
·
Science
·
667
Comparative genomic hybridization using oligonucleotide microarrays and total genomic DNA
2004
·
Michael T. Barrett
, Alicia Scheffer
, et al.
·
Proceedings of the National Academy of Sciences
·
367
The Fine-Scale and Complex Architecture of Human Copy-Number Variation
2008
·
George H. Perry
, Amir Ben-Dor
, et al.
·
The American Journal of Human Genetics
·
346
PDF
Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases
2007
·
Adam J. de Smith
, Anya Tsalenko
, et al.
·
Human Molecular Genetics
·
214
Characterization of missing human genome sequences and copy-number polymorphic insertions
2010
·
Jeffrey M Kidd
, Nick Sampas
, et al.
·
Nature Methods
·
151
PDF
Identification of endothelial cell genes by combined database mining and microarray analysis
2003
·
Michael Ho
, Eugene Yang
, et al.
·
Physiological Genomics
·
120
Population-Genetic Properties of Differentiated Human Copy-Number Polymorphisms
2011
·
Catarina D. Campbell
, Nick Sampas
, et al.
·
The American Journal of Human Genetics
·
90
PDF
Closing gaps in the human genome with fosmid resources generated from multiple individuals
2007
·
Donald Bovee
, Yang Zhou
, et al.
·
Nature Genetics
·
49
Increased LOH Resolution Achieved with the Addition of Comprehensive and Updated SNP Content on Agilent’s CGH +SNP Cancer and Postnatal Array Platform
2015
·
Anindita Dutta
, Jan Godoski
, et al.
·
Cancer Genetics
database mining and microarray analysis Identification of endothelial cell genes by combined
2015
·
Thomas Quertermous
, James Z. Wang
, et al.
Abstract 5095: CGH+SNP microarrays for copy-neutral aberration detection in cancer research
2012
·
Paula Costa
, Bo Curry
, et al.
·
Cancer Research
Abstract 45: Accurate total and allele-specific copy number measurements in mosaic tumors
2011
·
Bo Curry
, Nick Sampas
, et al.
·
Cancer Research
Feature extraction and clustering tools for analysing gene expression data from DNA microarrays
1999
·
Nick Sampas
, Zohar Yakhini
, et al.
·
Nature Genetics
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Works count:
15
Citation count:
3,121
H-index:
9
I10-index:
9
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