search.HSLS.MolBio About search.HSLS.MolBio

Databases/Tools

Find molecular databases and software tools with a combined search of the
HSLS Online Bioinformatics Resource Collection (OBRC) and the BioMed Central Databases collection.
Guided Tour

Articles on Databases/Tools

Find journal articles specifically on molecular databases and software tools using a filtered PubMed search.
Guided Tour

Genes/Proteins

Find information on genes and proteins with a combined search of NCBI Entrez Gene and the BIOBASE Knowledge Library*.
Guided Tour

Pathways

Find information on metabolic and signaling pathways with a combined search of NCBI BioSystems,
the Protein Lounge Pathway Database* and the Science STKE Database of Cell Signaling*.

Web

Find information on the Web using Clusty, the results clustering search engine.
Results 1-20 of about 331|
  1. Conduct protein classification, expression analysis and SNP function screening.
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  2. Contains mouse single nucleotide polymorphisms (SNPs) that are predicted to cause missense, nonsense, frameshift, or splice site mutations.
    Subject Areas: Genetics
    Content: Sequence, Gene, Curated
  3. ... for large-scale amplification and sequencing projects aimed at constructing single nucleotide polymorphisms (SNPs) maps.
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  4. Contains compound microsatellite-SNP markers in human, dog, mouse, rat and chicken.
    Subject Areas: Genetics, Genomics, Bioinformatics
    Content: Organism, Gene, SNP, Sequence, Curated
  5. Conduct genome-wide identification of SNPs in microorganisms.
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  6. A resource of genome-wide definitive haplotypes determined from a collection of Japanese complete hydatidiform moles (CHMs), each of which carries a genome derived from a single sperm.
    Subject Areas: Genetics, Genomics
    Content: DNA, Sequence, SNP, Curated
  7. Search for information on polymorphic genes in the immune system.
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  8. A database of human coding single nucleotide polymorphisms (SNPs) and their annotations. Integrates several coding SNPs (cSNPs) and protein-related information resources and predicts the implications of the non-synonymous SNPs (nsSNPs).
    Subject Areas: Genetics, Medical genetics
    Content: SNP, Disease, Curated, Sequence
  9. Find suitable restriction enzymes for assays on a batch of SNPs and genes from the human, rat, and mouse genomes.
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  10. A collection of all the existing polymorphic sequences in the Mammalia group. Search for any polymorphic set according to different parameter values of nucleotide diversity.
    Subject Areas: Genomics, Genetics
    Content: SNP, Sequence, Links to other sources
  11. Search for information on within-species sequence polymorphism in the nuclear, mitochondrial and chloroplastic genomes of Eukaryota species.
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  12. A comprehensive database of phenotypic and genotypic data from inbred mouse strains.
    Subject Areas: Genetics, Genomics
    Content: DNA/Organism stock, Sequence, SNP, Curated
  13. Search for naturally occurring DNA variations in putative microRNA target sites.
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  14. A database of human single nucleotide polymorphisms that cause premature termination codons and nonsense-mediated mRNA decay.
    Subject Areas: Genetics, Medical genetics
    Content: SNP, RNA, Curated, Sequence, Disease
  15. Optimize the selection of microbial forensic markers to maximize information gained from the fewest assays, accepting whole or partial genome sequence data as ...
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  16. A project to integrate gene, sequence and polymorphism data into individually annotated gene models. The human genes included are related to DNA repair, cell cycle control, cell signaling, cell division, homeostasis and metabolism, and are thought to play a role in susceptibility to environmental exposure.
    Subject Areas: Genetics, Genomics, Bioinformatics, Medical genetics
    Content: Gene, SNP, Sequence, Links to other sources, Curated
  17. Perform gene specific SNPs analysis for human genes.
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  18. Provides quick access to all data found in the dbSNP and HapMap databases, and includes specialized data from other projects. The database includes a suite of analysis tools such as linkage disequilibrium plots, tag SNPs and more. Users can also upload their own data and use the GVS analysis and visualization tools.
    Subject Areas: Genomics, Genetics, Bioinformatics
    Content: SNP, DNA, Gene, Sequence
  19. Integration of publicly available databases of human genetic variation with molecular features and clinical phenotype data.
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  20. A project that identifies relationships between environmental exposures, inter-individual sequence variation in human genes and disease risk in U.S. populations.
    Subject Areas: Medical genetics, Bioinformatics, Health services research, Public health
    Content: Disease, Gene, cDNA, SNP, Sequence, Links to other sources, Curated
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