dbSNP-Q
Names
More detailed information about this field from each metasource.
dbSNP-Q
metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657
metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:24.218623
dbsnp-q
metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:24.218623
Names
More detailed information about this field from each metasource.
dbSNP-Q
metasource: Nucleic Acid Research database catalogueversion: extracted_at: 2022-11-04T11:16:25.468657
metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:24.218623
dbsnp-q
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:34:24.218623
Names
More detailed information about this field from each metasource.
dbSNP-Q
metasource: Nucleic Acid Research database catalogueversion: extracted_at: 2022-11-04T11:16:25.468657
metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:24.218623
dbsnp-q
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:34:24.218623
This source may no longer be available. No known URL could be resolved successfully.
Description
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GWAS prioritization tool
metasource: Nucleic Acid Research database catalogueversion: extracted_at: 2022-11-04T11:16:25.468657
dbSNP-Q is a web application for working with the dbSNP relational database. dbSNP is a source of information on single nucleotide polymorphisms (SNPs) and other genetic variation for many different organisms, including humans. dbSNP-Q can be used to query human data from dbSNP for a variety tasks such as genomic mapping, SNP/gene functional properties, allele frequency data and information on the underlying experiments. It also includes documentation and download tools.
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:34:24.218623
Webpage:
http://cgsmd.isi.edu/dbsnpqWebpage
More detailed information about this field from each metasource.
http://cgsmd.isi.edu/dbsnpq
metasource: Nucleic Acid Research database catalogueversion: extracted_at: 2022-11-04T11:16:25.468657
metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:24.218623
Publications:
Publications
More detailed information about this field from each metasource.
New tools and methods for direct programmatic access to the dbSNP relational database
PMID: 21037260
metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:24.218623
http://nar.oxfordjournals.org/content/39/suppl_1/D901
metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657
Publications
More detailed information about this field from each metasource.
New tools and methods for direct programmatic access to the dbSNP relational database
PMID: 21037260
metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:24.218623
http://nar.oxfordjournals.org/content/39/suppl_1/D901
metasource: Nucleic Acid Research database catalogueversion: extracted_at: 2022-11-04T11:16:25.468657
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New tools and methods for direct programmatic access to the dbSNP relational database
PubMed citations: 13.
13 articles citing: New tools and methods for direct programmatic access to the dbSNP relational database
Tumor somatic mutations also existing as germline polymorphisms may help to identify functional SNPs from genome-wide association studies. PMID:32681635
The BIG Data Center: from deposition to integration to translation. PMID:27899658
Constructing a Genome-Wide LD Map of Wild A. gambiae Using Next-Generation Sequencing. PMID:26421280
Genetic and non-genetic determinants of raltegravir penetration into cerebrospinal fluid: a single arm pharmacokinetic study. PMID:24349334
Genomics meets proteomics: identifying the culprits in disease. PMID:24135908
Candidate gene association studies: a comprehensive guide to useful in silico tools. PMID:23656885
Probabilistic error correction for RNA sequencing. PMID:23558750
Testing for associations between loci and environmental gradients using latent factor mixed models. PMID:23543094
TIARA genome database: update 2013. PMID:23515433
A map of human microRNA variation uncovers unexpectedly high levels of variability. PMID:22906193
Accurate reconstruction of insertion-deletion histories by statistical phylogenetics. PMID:22536326
BioQ: tracing experimental origins in public genomic databases using a novel data provenance model. PMID:22426342
GWASdb: a database for human genetic variants identified by genome-wide association studies. PMID:22139925 - http://nar.oxfordjournals.org/content/39/suppl_1/D901
Tags:
Tags
More detailed information about this field from each metasource.
human genes and diseases
metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657
general human genetics databases
metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657
genetic variation
metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:24.218623
dna polymorphism
metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:24.218623
model organisms
metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:24.218623
mapping
metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:24.218623
Tags
More detailed information about this field from each metasource.
human genes and diseases
metasource: Nucleic Acid Research database catalogueversion: extracted_at: 2022-11-04T11:16:25.468657
general human genetics databases
metasource: Nucleic Acid Research database catalogueversion: extracted_at: 2022-11-04T11:16:25.468657
genetic variation
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:34:24.218623
dna polymorphism
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:34:24.218623
model organisms
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:34:24.218623
mapping
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:34:24.218623
human genes and diseases general human genetics genetic variation dna polymorphism model organisms mapping
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