> > Health and Disease

Health and Disease

Resources in this section encompass genomic research related to human health and disease.

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Found 29 links

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Canada Health InfowayResource Content

https://www.infoway-inforoute.ca/

Education > Community
Human Genome > Health and Disease

Canada Health Infoway is working to develop a network of electronic health records across Canada in order to improve the quality and access to healthcare services, therefore making them more productive.

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Cancer Genome Anatomy ProjectTool Content

http://cgap.nci.nih.gov/

DNA > Sequence Polymorphisms
Expression > cDNA, EST, SAGE
Human Genome > Health and Disease
Human Genome > Sequence Polymorphisms
Model Organisms > Other Vertebrates

Goal is to determine the gene expression profiles of normal, precancer, and cancer cells; resources for human and mouse include ESTs, gene expression patterns, SNPs, cluster assemblies, cytogenetic information, and tools to query and analyze the data.

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tagsgene library human genome project humans neoplasms

CanPredictTool Content

http://www.cgl.ucsf.edu/Research/genentech/canpredict/

Human Genome > Health and Disease
Human Genome > Sequence Polymorphisms
Protein > Sequence Features

CanPredict uses a combination of computational methods to predict whether specific sequence changes in a protein are likely to be cancer-associated mutations.

NAR Web Server Issue 2007
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tagsalgorithms alleles amino acids computational biology expressed sequence tags genetic predisposition to disease humans missense mutation neoplasm dna neoplasms single nucleotide polymorphism tumor cell line

CARGOTool Content

http://cargo2.bioinfo.cnio.es/docs/aboutCargo.html

DNA > Annotations
DNA > Sequence Polymorphisms
Human Genome > Annotations
Human Genome > Health and Disease
Human Genome > Sequence Polymorphisms
Literature > Text Mining and Semantics
Protein > Interactions, Pathways, Enzymes

CARGO (Cancer And Related Genes Online) is a portal that uses widgets to allow users to mine literature using iHOP, retrieve disease information from OMIM, visualize 3D SNPs, query protein interactions, and view summarized gene annotation information for cancer related genes in human.

NAR Web Server Issue 2007
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tagsanimals biology computational biology database management systems factual databases genetic databases humans programming languages systems integration

DyNAVacSTool Content

http://miracle.igib.res.in/dynavac/

DNA > Tools For the Bench
Human Genome > Health and Disease

DyNAVacS is a tool for designing DNA vaccines that includes steps for chosing a suitable expression vector, ensuring optimal expression by codon optimization, engineering CpG motifs for enhancing immune responses, and providing additional sequence signals for efficient translation. It also allows includes restriction enzyme mapping and design of primers spanning user specified sequences.

NAR Web Server Issue 2006
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tagscodon computational biology cpg islands dna primers dna vaccines drug design gene expression polymerase chain reaction restriction mapping systems integration

EpiToolKitTool Content

http://www.epitoolkit.org

Human Genome > Health and Disease
Human Genome > Sequence Polymorphisms
Protein > Molecular Dynamics and Docking

A suite of tools for immunological research. EpiToolKit offers a variety of prediction methods that may be run simultaneously for predicting MHC Class I and II ligands, and minor histocompatibility antigens. The influence of sequence polymorphisms or mutations on potential T-cell epitopes may also be examined.

NAR Web Server Issue 2008
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tagsacetaminophen child computational biology dosage forms drug packaging france genetic polymorphism histocompatibility antigens humans ligands mutation neoplasm antigens non-narcotic analgesics oral administration peptides poison control centers poisoning protein sequence analysis t-lymphocyte epitopes

FluGenomeTool Content

http://www.flugenome.org/

Human Genome > Health and Disease
Model Organisms > Other Organisms
Sequence Comparison > Similarity Searching

FluGenome is a tool for determining lineages and genotypes of influenza A viruses.

NAR Web Server Issue 2007
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tagscomputational biology genetic databases genetic polymorphism genomics genotype influenza a virus orthomyxoviridae phylogeny viral genes viral genome viral proteins

G2DTool Content

http://www.ogic.ca/projects/g2d_2/

Human Genome > Health and Disease

G2D (Candidate Genes to Inherited Diseases) scans a human genomic region for genes related to an inherited disease. The G2D server also presents precomputed candidate genes for more than 600 genetically inherited diseases that have been mapped onto chromosomal regions without assignment of a particular gene.

NAR Web Server Issue 2007
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tagsalgorithms alzheimer disease asthma chromosome mapping computational biology genes genetic databases genetic linkage genetic markers genetic predisposition to disease human genome humans inborn genetic diseases mathematics medline obesity phenotype type 2 diabetes mellitus

GeneCardsDatabase Content

http://www.genecards.org/

Human Genome > Health and Disease

Database of human genes, their products, and involvement in diseases; free for non-commercial use, but users should also read the Terms of Use for this site.

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tagsfactual databases human genome project humans

GeneSeekerTool Content

http://www.cmbi.ru.nl/GeneSeeker/

Human Genome > Health and Disease

GeneSeeker allows you to generate a list of candidate genes related to a human genetic disorder by searching against localization and expression databases.

NAR Web Server Issue 2005
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tagschromosome mapping gene expression genetic databases genetic predisposition to disease humans inborn genetic diseases phenotype syndrome systems integration

GeneTestsDatabase Content

http://www.geneclinics.org/

Human Genome > Health and Disease

GeneTests is a medical genetics information resource developed for physicians, other healthcare providers, and researchers, available at no cost to all interested persons

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GenoWatchTool Content

http://genepipe.ngc.sinica.edu.tw/genowatch

Human Genome > Health and Disease
Human Genome > Sequence Polymorphisms

A disease gene mining browser for association study. GenoWatch is a real-time batch SNP and short tandem repeat polymorphism pipeline that extracts current information from public domain websites such as NCBI, UniProt, KEGG and GO so that users can select the appropriate disease candidate genes.

NAR Web Server Issue 2008
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tagschromosome mapping genes genetic databases genetic markers genetic polymorphism human genome humans inborn genetic diseases microsatellite repeats pubmed single nucleotide polymorphism

GeSBAPTool Content

http://bioinfo.cipf.es/gesbap/

Expression > Gene Set Analysis
Human Genome > Health and Disease
Human Genome > Sequence Polymorphisms

Gene Set based Analysis of Polymorphisms (GeSBAP) implements the gene set analysis to the evaluation of genome wide association studies. Gene set analysis is based on testing the association of modules of functionally related genes.

NAR Web Server Issue 2009
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tagsbiological processes breast neoplasms female genes genetic variation genome-wide association study humans single nucleotide polymorphism

HomozygosityMapperTool Content

http://www.homozygositymapper.org

DNA > Sequence Polymorphisms
Human Genome > Health and Disease
Human Genome > Sequence Polymorphisms

A web base approach to homozygosity mapping. Users upload SNP genotype files into a marker database for analysis and detection of long homozygous stretches.

NAR Web Server Issue 2009
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tagschromosome mapping genetic heterogeneity genetic linkage genotype homozygote reproducibility of results single nucleotide polymorphism

Human Gene Mutation DatabaseDatabase Content

http://www.hgmd.cf.ac.uk/ac/index.php

Human Genome > Health and Disease

The Human Gene Mutation Database comprises various types of mutation within the coding regions of human nuclear genes causing inherited disease.

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tagsbase sequence database management systems dna mutational analysis dna sequence analysis genes genetic databases genetic polymorphism genomics human genome humans molecular sequence data mutation single nucleotide polymorphism time factors

Tags associated with subcategory 'Human Genome/Health and Disease'

humans genetic databases computational biology genetic predisposition to disease genetic polymorphism single nucleotide polymorphism inborn genetic diseases human genome genomics peptides algorithms genes type 2 diabetes mellitus oligonucleotide array sequence analysis thyroid neoplasms cpg islands protein sequence analysis gene expression polymerase chain reaction drug design dna vaccines tertiary protein structure obesity dna primers genetic markers medline phylogeny viral genes orthomyxoviridae influenza a virus t-lymphocyte epitopes genotype viral genome viral proteins restriction mapping mathematics chromosome mapping asthma amino acids expressed sequence tags automation programming languages mice neoplasm proteins gene expression profiling time factors roc curve statistical models protein isoforms tissue distribution neoplasm dna tumor cell line missense mutation systems integration phenotype syndrome research design reproducibility of results decision trees dna sequence analysis conserved sequence poisoning National Center for Biotechnology Information (NCBI) gene library human genome project genetic linkage nucleic acid databases protein databases linkage disequilibrium genome genetic models genetic testing poison control centers neoplasms restriction fragment length polymorphism tuberculosis factual databases database management systems codon biology biomedical research cluster analysis major histocompatibility complex subunit vaccines vaccines proteasome endopeptidase complex huntington disease schizophrenia hla-b antigens alzheimer disease child microbial sensitivity tests minisatellite repeats interspersed repetitive sequences dna fingerprinting dna mutational analysis molecular sequence data bacterial dna molecular epidemiology mycobacterium tuberculosis b-lymphocyte epitopes