Published in Nat Biotechnol on August 01, 2012
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Combing of genomic DNA from droplets containing picograms of material. ACS Nano (2015) 0.79
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CRISPR-CAS9 D10A nickase target-specific fluorescent labeling of double strand DNA for whole genome mapping and structural variation analysis. Nucleic Acids Res (2015) 0.79
Measurements of DNA barcode label separations in nanochannels from time-series data. Biomicrofluidics (2015) 0.79
Experimental evidence of weak excluded volume effects for nanochannel confined DNA. ACS Macro Lett (2015) 0.79
Bacteriophage strain typing by rapid single molecule analysis. Nucleic Acids Res (2015) 0.78
Single-molecule optical genome mapping of a human HapMap and a colorectal cancer cell line. Gigascience (2015) 0.78
A Nanofluidic Biosensor Based on Nanoreplica Molding Photonic Crystal. Nanoscale Res Lett (2016) 0.78
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Optical mapping in plant comparative genomics. Gigascience (2015) 0.78
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Construction of a map-based reference genome sequence for barley, Hordeum vulgare L. Sci Data (2017) 0.78
An advanced reference genome of Trifolium subterraneum L. reveals genes related to agronomic performance. Plant Biotechnol J (2017) 0.77
Modeling the relaxation of internal DNA segments during genome mapping in nanochannels. Biomicrofluidics (2016) 0.77
Rapid identification of intact bacterial resistance plasmids via optical mapping of single DNA molecules. Sci Rep (2016) 0.77
Rapid construction of genome map for large yellow croaker (Larimichthys crocea) by the whole-genome mapping in BioNano Genomics Irys system. BMC Genomics (2015) 0.77
Visualizing the entire DNA from a chromosome in a single frame. Biomicrofluidics (2015) 0.77
DNA: stretch for the camera. Nat Methods (2012) 0.75
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DNA origami-based shape IDs for single-molecule nanomechanical genotyping. Nat Commun (2017) 0.75
Wafer-scale integration of sacrificial nanofluidic chips for detecting and manipulating single DNA molecules. Nat Commun (2017) 0.75
A novel 2D silicon nano-mold fabrication technique for linear nanochannels over a 4 inch diameter substrate. Sci Rep (2016) 0.75
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Analysis of single nucleic acid molecules in micro- and nano-fluidics. Lab Chip (2016) 0.75
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Interchromosomal core duplicons drive both evolutionary instability and disease susceptibility of the Chromosome 8p23.1 region. Genome Res (2016) 0.75
Thermoplastic nanofluidic devices for biomedical applications. Lab Chip (2016) 0.75
DNA compaction by the bacteriophage protein Cox studied on the single DNA molecule level using nanofluidic channels. Nucleic Acids Res (2016) 0.75
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OMWare: a tool for efficient assembly of genome-wide physical maps. BMC Bioinformatics (2016) 0.75
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Interference of ATP with the fluorescent probes YOYO-1 andYOYO-3 modifies the mechanical properties of intercalator-stained DNA confined in nanochannels. Mikrochim Acta (2015) 0.75
A Simple Thermoplastic Substrate Containing Hierarchical Silica Lamellae for High-Molecular-Weight DNA Extraction. Adv Mater (2016) 0.75
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Whole-Genome Restriction Mapping by "Subhaploid"-Based RAD Sequencing: An Efficient and Flexible Approach for Physical Mapping and Genome Scaffolding. Genetics (2017) 0.75
Strategies for optimizing BioNano and Dovetail explored through a second reference quality assembly for the legume model, Medicago truncatula. BMC Genomics (2017) 0.75
Enhanced nanochannel translocation and localization of genomic DNA molecules using three-dimensional nanofunnels. Nat Commun (2017) 0.75
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Simulations of knotting of DNA during genome mapping. Biomicrofluidics (2017) 0.75
Advances in Decoding Axolotl Limb Regeneration. Trends Genet (2017) 0.75
Electrophoretic stretching and imaging of single native chromatin fibers in nanoslits. Biomicrofluidics (2017) 0.75
Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biol (2009) 235.12
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DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome. Nature (2008) 38.13
Large-scale copy number polymorphism in the human genome. Science (2004) 34.64
Mapping and sequencing of structural variation from eight human genomes. Nature (2008) 30.28
Structural variation in the human genome. Nat Rev Genet (2006) 21.40
Complete MHC haplotype sequencing for common disease gene mapping. Genome Res (2004) 12.09
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Computational methods for discovering structural variation with next-generation sequencing. Nat Methods (2009) 7.20
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Variation analysis and gene annotation of eight MHC haplotypes: the MHC Haplotype Project. Immunogenetics (2008) 4.25
From the Cover: The dynamics of genomic-length DNA molecules in 100-nm channels. Proc Natl Acad Sci U S A (2004) 3.65
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Defining the role of the MHC in autoimmunity: a review and pooled analysis. PLoS Genet (2008) 3.54
Optical mapping as a routine tool for bacterial genome sequence finishing. BMC Genomics (2007) 2.71
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A comprehensively molecular haplotype-resolved genome of a European individual. Genome Res (2011) 1.83
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Sequence capture and next generation resequencing of the MHC region highlights potential transplantation determinants in HLA identical haematopoietic stem cell transplantation. DNA Res (2011) 1.00
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Genome-wide detection and characterization of positive selection in human populations. Nature (2007) 17.27
Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. Nat Genet (2009) 9.45
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Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis. Nat Genet (2009) 5.93
A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci. PLoS Genet (2008) 5.85
The draft genome of the transgenic tropical fruit tree papaya (Carica papaya Linnaeus). Nature (2008) 5.54
A common BIM deletion polymorphism mediates intrinsic resistance and inferior responses to tyrosine kinase inhibitors in cancer. Nat Med (2012) 4.90
Exome sequencing of gastric adenocarcinoma identifies recurrent somatic mutations in cell adhesion and chromatin remodeling genes. Nat Genet (2012) 4.82
Multiple polymorphisms in the TNFAIP3 region are independently associated with systemic lupus erythematosus. Nat Genet (2008) 4.33
Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis. Nature (2010) 3.90
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A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis. Nat Genet (2003) 3.52
Narcolepsy is strongly associated with the T-cell receptor alpha locus. Nat Genet (2009) 3.33
Population stratification confounds genetic association studies among Latinos. Hum Genet (2005) 3.19
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Admixture mapping of an allele affecting interleukin 6 soluble receptor and interleukin 6 levels. Am J Hum Genet (2007) 2.91
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Temporal dissection of tumorigenesis in primary cancers. Cancer Discov (2011) 2.40
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Comprehensive long-span paired-end-tag mapping reveals characteristic patterns of structural variations in epithelial cancer genomes. Genome Res (2011) 1.67
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Rapid DNA mapping by fluorescent single molecule detection. Nucleic Acids Res (2006) 1.63
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An ethical solution to the challenges in teaching anatomy with dissection in the Chinese culture. Anat Sci Educ (2009) 1.47
ADAM33 is not associated with asthma in Puerto Rican or Mexican populations. Am J Respir Crit Care Med (2003) 1.47
Rapid genome mapping in nanochannel arrays for highly complete and accurate de novo sequence assembly of the complex Aegilops tauschii genome. PLoS One (2013) 1.44
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Direct determination of haplotypes from single DNA molecules. Nat Methods (2009) 1.30
High-density single-nucleotide polymorphism maps of the human genome. Genomics (2005) 1.27
A genetic risk score combining ten psoriasis risk loci improves disease prediction. PLoS One (2011) 1.25
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Novel immunoglobulin superfamily gene cluster, mapping to a region of human chromosome 17q25, linked to psoriasis susceptibility. Hum Genet (2002) 1.24
Polymorphisms in transforming growth factor-beta-related genes ALK1 and ENG are associated with sporadic brain arteriovenous malformations. Stroke (2005) 1.21
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Is altered expression of hepatic insulin-related genes in growth hormone receptor knockout mice due to GH resistance or a difference in biological life spans? J Gerontol A Biol Sci Med Sci (2009) 1.09
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Pharmacogenomic assessment of carboxylesterases 1 and 2. Genomics (2004) 1.09
Polymorphism discovery in 51 chemotherapy pathway genes. Hum Mol Genet (2005) 1.09
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Single-molecule analysis for molecular haplotyping. Hum Mutat (2004) 1.06
Identification of a frequent variant in ALG6, the cause of Congenital Disorder of Glycosylation-Ic. Hum Mutat (2003) 1.05
Further genetic evidence for three psoriasis-risk genes: ADAM33, CDKAL1, and PTPN22. J Invest Dermatol (2008) 1.04
Gene-trapped mouse embryonic stem cell-derived cardiac myocytes and human genetics implicate AKAP10 in heart rhythm regulation. Proc Natl Acad Sci U S A (2007) 1.04
Natural variation in four human collagen genes across an ethnically diverse population. Genomics (2008) 1.03
An apolipoprotein A-V gene SNP is associated with marked hypertriglyceridemia among Asian-American patients. J Lipid Res (2008) 1.02
OATP1B1-related drug-drug and drug-gene interactions as potential risk factors for cerivastatin-induced rhabdomyolysis. Pharmacogenet Genomics (2013) 1.02
African ancestry, socioeconomic status, and kidney function in elderly African Americans: a genetic admixture analysis. J Am Soc Nephrol (2006) 1.02
Functional genetic variation in the basal promoter of the organic cation/carnitine transporters OCTN1 (SLC22A4) and OCTN2 (SLC22A5). J Pharmacol Exp Ther (2009) 1.01
Apolipoprotein E epsilon 2 is associated with new hemorrhage risk in brain arteriovenous malformations. Neurosurgery (2006) 1.01
Paternal origins of complete hydatidiform moles proven by whole genome single-nucleotide polymorphism haplotyping. Genomics (2002) 1.01