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An SNP map of the human genome generated by reduced representation shotgun sequencing
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Single nucleotide polymorphism hunting in cyberspace
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Basic Local Alignment Search Tool
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Characterization of single-nucleotide polymorphisms in coding regions of human genes
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Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis
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Reliable identification of large numbers of candidate SNPs from public EST data
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A general approach to single-nucleotide polymorphism discovery
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Prospects for whole-genome linkage disequilibrium mapping of common disease genes
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Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland
inferredcites →https://doi.org/10.1073/pnas.96.26.15173openalex-snapshot
Genetic epidemiology of single-nucleotide polymorphisms
inferredcites →https://doi.org/10.1086/302448openalex-snapshot
Sequence Diversity in 36 Candidate Genes for Cardiovascular Disorders
inferredcites →https://doi.org/10.1093/genetics/129.2.513openalex-snapshot
Low nucleotide diversity in man.
inferredcites →https://doi.org/10.1101/gr.7.5.401openalex-snapshot
Human Whole-Genome Shotgun Sequencing
inferredcites →https://doi.org/10.1101/gr.8.12.1229openalex-snapshot
A DNA Polymorphism Discovery Resource for Research on Human Genetic Variation: Table 1.
inferredcites →https://doi.org/10.1101/gr.8.3.175openalex-snapshot
Base-Calling of Automated Sequencer Traces Using Phred. I. Accuracy Assessment
inferredcites →https://doi.org/10.1101/gr.8.3.186openalex-snapshot
Base-Calling of Automated Sequencer Traces Using Phred. II. Error Probabilities
inferredcites →https://doi.org/10.1101/gr.8.8.769openalex-snapshot
Reading Bits of Genetic Information: Methods for Single-Nucleotide Polymorphism Analysis
inferredcites →https://doi.org/10.1126/science.273.5281.1516openalex-snapshot
The Future of Genetic Studies of Complex Human Diseases
inferredcites →https://doi.org/10.1126/science.274.5287.536openalex-snapshot
The New Genomics: Global Views of Biology
inferredcites →https://doi.org/10.1126/science.278.5343.1580openalex-snapshot
Variations on a Theme: Cataloging Human DNA Sequence Variation
inferredcites →https://doi.org/10.1126/science.280.5366.1077openalex-snapshot
Large-Scale Identification, Mapping, and Genotyping of Single-Nucleotide Polymorphisms in the Human Genome
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Pharmacogenetics: Implications of race and ethnicity on defining genetic profiles for personalized medicine
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Diagnostic DNA markers for quality traits in wheat
inferred← citeshttps://doi.org/10.1016/j.meatsci.2020.108152openalex-snapshot
Development of a 64 SNV panel for breed authentication in Iberian pigs and their derived meat products
inferred← citeshttps://doi.org/10.1016/j.molp.2015.02.002openalex-snapshot
Single Nucleotide Polymorphism Identification in Polyploids: A Review, Example, and Recommendations
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2005.01.006openalex-snapshot
Genetic association studies of complex traits: design and analysis issues
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2015.03.014openalex-snapshot
High-throughput sequencing in mutation detection: A new generation of genotoxicity tests?
inferred← citeshttps://doi.org/10.1016/j.mrrev.2011.11.002openalex-snapshot
Whole genome sequencing for quantifying germline mutation frequency in humans and model species: Cautious optimism
inferred← citeshttps://doi.org/10.1016/j.nbt.2012.11.015openalex-snapshot
The SNPs in the human genetic blueprint era
inferred← citeshttps://doi.org/10.1016/j.pestbp.2020.104717openalex-snapshot
Unique genetic variants in dihydrolipoamide dehydrogenase (dld) gene confer strong resistance to phosphine in the rusty grain beetle, Cryptolestes ferrugineus (Stephens)
inferred← citeshttps://doi.org/10.1016/j.psj.2022.102203openalex-snapshot
Low-coverage sequencing in a deep intercross of the Virginia body weight lines provides insight to the polygenic genetic architecture of growth: novel loci revealed by increased power and improved genome-coverage
inferred← citeshttps://doi.org/10.1016/j.sbspro.2015.08.024openalex-snapshot
Culture-specific Subjective Evaluation of Character Strengths
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2019.134560openalex-snapshot
Plant and soil traits driving soil fungal community due to tree plantation on the Loess Plateau
inferred← citeshttps://doi.org/10.1016/j.snb.2006.04.064openalex-snapshot
DNA biosensor using fluorescence microscopy and impedance spectroscopy
inferred← citeshttps://doi.org/10.1016/j.snb.2007.04.020openalex-snapshot
A novel detection method for DNA point mutation using QCM based on Fe3O4/Au core/shell nanoparticle and DNA ligase reaction
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2018.06.028openalex-snapshot
Effect of dietary energy restriction and subsequent compensatory feeding on testicular transcriptome in developing rams
inferred← citeshttps://doi.org/10.1016/j.ygeno.2019.11.015openalex-snapshot
Construction of a high-density genetic map with whole genome sequencing in Nicotiana tabacum L
inferred← citeshttps://doi.org/10.1016/j.ympev.2011.10.012openalex-snapshot
Next-generation sequencing reveals phylogeographic structure and a species tree for recent bird divergences
inferred← citeshttps://doi.org/10.1016/j.ympev.2011.12.007openalex-snapshot
Applications of next-generation sequencing to phylogeography and phylogenetics
inferred← citeshttps://doi.org/10.1016/j.ympev.2014.06.026openalex-snapshot
Genotyping-by-sequencing as a tool to infer phylogeny and ancestral hybridization: A case study in Carex (Cyperaceae)
inferred← citeshttps://doi.org/10.1016/j.ympev.2017.07.018openalex-snapshot
Species trees from consensus single nucleotide polymorphism (SNP) data: Testing phylogenetic approaches with simulated and empirical data
inferred← citeshttps://doi.org/10.1016/s0065-2458(03)60006-9openalex-snapshot
Shotgun Sequence Assembly
inferred← citeshttps://doi.org/10.1016/s0065-2660(06)57002-6openalex-snapshot
Enabling a Community to Dissect an Organism: Overview of the Neurospora Functional Genomics Project
inferred← citeshttps://doi.org/10.1016/s0065-7743(01)36060-8openalex-snapshot
Chapter 20. Bioinformatics in the drug discovery process
inferred← citeshttps://doi.org/10.1016/s0065-7743(03)38026-1openalex-snapshot
Chapter 25. SNPs: A human genetic tool for the new millennium
inferred← citeshttps://doi.org/10.1016/s0166-2236(00)01866-xopenalex-snapshot
Neuroscience in the post-genome era: an overview
inferred← citeshttps://doi.org/10.1016/s0168-9525(00)02109-0openalex-snapshot
Genomics – the new rock and roll?
inferred← citeshttps://doi.org/10.1016/s0378-1119(03)00628-0openalex-snapshot
Low hanging fruit: A subset of human cSNPs is both highly non-uniform and predictable
inferred← citeshttps://doi.org/10.1016/s0531-5131(01)00570-2openalex-snapshot
The Human Genome Project and its importance in clinical medicine
inferred← citeshttps://doi.org/10.1016/s0531-5565(01)00091-2openalex-snapshot
DNA-microarrays: novel techniques to study aging and guide gerontologic medicine
inferred← citeshttps://doi.org/10.1016/s0896-8411(03)00094-5openalex-snapshot
Genetic analysis of multiple sclerosis
inferred← citeshttps://doi.org/10.1016/s0959-437x(00)00185-4openalex-snapshot
Chromosome 21: from sequence to applications
inferred← citeshttps://doi.org/10.1016/s0959-4388(00)00261-0openalex-snapshot
SNP analysis to dissect human traits
inferred← citeshttps://doi.org/10.1016/s1344-6223(02)00031-7openalex-snapshot
The evolution and formation of RH genes
inferred← citeshttps://doi.org/10.1016/s1367-5931(00)00171-xopenalex-snapshot
SNPing in the human genome
inferred← citeshttps://doi.org/10.1016/s1367-5931(01)00285-xopenalex-snapshot
High-density genotyping and linkage disequilibrium in the human genome using chromosome 22 as a model
inferred← citeshttps://doi.org/10.1016/s1570-0232(02)00699-2openalex-snapshot
Sequence variation and the biological function of genes: methodological and biological considerations
inferred← citeshttps://doi.org/10.1016/s1570-0232(02)00700-6openalex-snapshot
A decade of high-resolution liquid chromatography of nucleic acids on styrene–divinylbenzene copolymers
inferred← citeshttps://doi.org/10.1016/s1672-0229(05)03021-4openalex-snapshot
Neighboring-Nucleotide Effects on the Mutation Patterns of the Rice Genome
inferred← citeshttps://doi.org/10.1016/s1874-5334(04)80004-2openalex-snapshot
The Development of Genetic Markers from Fungal Genome Initiatives
inferred← citeshttps://doi.org/10.1016/s2212-5671(15)01429-xopenalex-snapshot
The making of Knowledge Cities in Romania
inferred← citeshttps://doi.org/10.1017/s146239940200491xopenalex-snapshot
Breast cancer gene discovery
inferred← citeshttps://doi.org/10.1021/ac049396dopenalex-snapshot
Electrokinetically Controlled DNA Hybridization Microfluidic Chip Enabling Rapid Target Analysis
inferred← citeshttps://doi.org/10.1021/ac0520386openalex-snapshot
Identification of Base Pairs in Single-Nucleotide Polymorphisms by MutS Protein-Mediated Capillary Electrophoresis
inferred← citeshttps://doi.org/10.1021/acs.accounts.1c00770openalex-snapshot
Single-Molecule Mechanochemical Sensing
inferred← citeshttps://doi.org/10.1021/es503189gopenalex-snapshot
Sequencing Human Mitochondrial Hypervariable Region II as a Molecular Fingerprint for Environmental Waters
inferred← citeshttps://doi.org/10.1021/ja0295220openalex-snapshot
PNA for One-Base Differentiating Protection of DNA from Nuclease and Its Use for SNPs Detection
inferred← citeshttps://doi.org/10.1021/ja201976ropenalex-snapshot
Detection of Single Nucleotide Polymorphism Using Tension-Dependent Stochastic Behavior of a Single-Molecule Template
inferred← citeshttps://doi.org/10.1029/2025wr040498openalex-snapshot
Eco‐Evo‐Hydraulics: Integrating Fish Evolution Into Ecohydraulics for Conservation
inferred← citeshttps://doi.org/10.1037/10480-008openalex-snapshot
An integrative neuroscience program linking mouse genes to cognition and disease.
inferred← citeshttps://doi.org/10.1038/35052543openalex-snapshot
Association study designs for complex diseases
inferred← citeshttps://doi.org/10.1038/35057062openalex-snapshot
Initial sequencing and analysis of the human genome
inferred← citeshttps://doi.org/10.1038/35057149openalex-snapshot
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
inferred← citeshttps://doi.org/10.1038/86864openalex-snapshot
Single-nucleotide polymorphisms in the public domain: how useful are they?
inferred← citeshttps://doi.org/10.1038/eye.2001.144openalex-snapshot
Strategies for mapping susceptibility genes in age-related maculopathy
inferred← citeshttps://doi.org/10.1038/hdy.2011.111openalex-snapshot
Types, levels and patterns of low-copy DNA sequence divergence, and phylogenetic implications, for Gossypium genome types
inferred← citeshttps://doi.org/10.1038/ismej.2015.162openalex-snapshot
Metagenomic reconstructions of bacterial CRISPR loci constrain population histories
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