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Goals include DNA sequencing, assembly of complete high-resolution (0.1 Mb) maps of chromosome 16 and regions of chromosome 5, studies at the molecular level of chromosome structure and function, and isolation of selected genes of interest.
Summarizes all known sequence variations in the human genome, to facilitate research into how genotypes affect common diseases, drug responses, and other complex phenotypes.
A database of human XSCID mutations (IL2RGbase) has been assembled. Information on new mutations may be submitted online
A database of clustered and assembled partial gene sequences (ESTs) and mRNA sequences from human and mouse. Its goal is to become a comprehensive cross-species gene index.
Database maintained by the Institute of Medical Genetics in Cardiff. Database query, statistics, project background and resource links.
This application consists of three separate databases of human and mouse malformation syndromes together with a database of mouse/human syntenic regions. The mouse and human malformation databases are linked together through the chromosome synte.
Aims to generate comprehensive representation of the sequence of each of the expressed genes in the human genome, by extensive processing of gene fragments to make accurate alignments, highlight diversity and provide a carefully joined set of c.
The purpose of IXDB is to provide an integrated view of the X chromosome mapping field. Ultimately this will allow the construction of an integrated map that will take into account all the data generated by the community, including physical, gen.
This site provides data and tools for studying the function of DNA sequences, with an emphasis on those involved in the production of hemoglobin.
Information on chromosome 15 sequencing project.
A relational database containing yeast RNA expression data.
Fundamental information on the structure and function of genes has been accumulated and is available to the public.
The purpose of the RH Server is to allow users to anonymously submit STSs to see which SHGC-typed markers on either the G3 or the TNG panels are closest to the user's submitted marker. Users can then attempt to place their markers on the SHGC G3.
Broken down by symbol, aliases, accession ID, and cytogenic location.
Genetic maps displayed at this site now reflect the final Genethon genetic linkage map of the genome published in Nature.
From Silverman Laboratory of Children's Hospital. Contains links to Chromosom 18 related sites.
From the National Center for Biotechnology Information.
Cytogenetic map location of disease genes and other expressed genes described in OMIM.
Genetic maps showing the positions of genetic markers, in addition to CHLC project information and publications.
This page contains links to a preliminary assembly of the current draft of the human genome. The human genome is approximately 3.1 billion bases. Roughly 87% of the genome has been sequenced by the International Human Genome Project.
A collection of curated databases containing DNA and protein sequence, gene expression, cellular role, protein family, and taxonomic data for microbes, plants and humans.
The glandular organ development database.
Effort to understanding of how genetic factors contribute to human disease.
Software and databases for mutations in human genes.
Published by the Sanger Centre, map and project information.
Compilation of aberrant splicing phenomena.
This database has been constructed for the use of all researchers who need easy and rapid access to kinetoplast minicircle sequences.
This database is dedicated to the nuclear genes specifying the enzymes, structural proteins, and other proteins, many still not identified, involved in mitochondrial biogenesis and function.
Washington University. Focused on the mapping and analysis of the X chromosome.
Access to the chromosome projects that have been sequenced at Institute of Molecular Biotechnology.
A data analysis and storage system for genomic sequence and its annotation. As a data analysis engine it accepts raw genomic sequence and automatically adds significant annotation. As a data storage system, it incorporates such sequence and anno.
Computerized databases containing chemical structures and biological data have been established at the Division of AIDS (DAIDS) NIAID to monitor developments in the chemotherapy of HIV and opportunistic infections (OI's) and to serve as an infor.
SNP database, genetic map of the human genome and map statistics.
produced by the International Albinism Center at the University of Minnesota. This database includes mutations associated with all major known forms of oculocutaneous and ocular albinism. The Albinism Database is part of the HUGO Mutation Databa.
This site is provided as a single-source launchpad to information about each human chromosome.
From Los Alamos National Laboratory, conducting genomic sequencing of human DNA.
At the Lawrence Berkeley National Laboratory is focused on the task of trying to add biological value to the raw data being generated by the Human Genome Project.
Posted by the National Humna Genome Research Institute.
An international collaboration in support of the Human Genome Project.
Genome database, project information, and staff information.
Protein database has been created to publicize the fruits of our Human cDNA project at the Kazusa DNA Research Institute. In this project, we plan to sequence and analyze long (>4 kb) human cDNAs and to establish methods by using the sequence da.
Contains information about genes which are targets for cancer-causing mutations; proto-oncogenes and tumor suppressor genes. Its goal is to provide a standard set of facts (e.g. protein size, biochemical activity, chromosomal location, .) abou.
A database of human genes, their products and their involvement in diseases. It offers concise information about the functions of all human genes that have an approved symbol, as well as selected others.
Links to homepages of labs, local biological applications, linkage maps to the human genome, computer support and protocols.
Data bank of expression information of human and mouse genes in various tissues or cell types.
Established the dbSNP database to serve as a central repository for both single base nucleotide subsitutions and short deletion and insertion polymorphisms.
A compendium of polymorphisms and mutations of the human mitochondrial DNA.
Provides access to leading-edge tools for research in the fields of genomics, genetics and functional genomics. It is located on the Hinxton Genome Campus along with the Sanger Centre and the European Bioinformatics Institute.
Archive of experimentally determined 3-D structures of HIV1 and HIV2, and SIV proteases and their complexes.
Cloned and/or mapped genes causing retinal diseases.
An international collaboration in support of the Human Genome Project.
This database has been initiated to collect data on mutations and polymorphisms in the X-ALD (ABCD1) gene. The aim of this website is to make this information readily accessible and to provide an easy way for reporting new X-ALD mutations.
Genome project list and links to genomic information and database.
Compiles the information relevant to the mapping efforts of the Human Genome Project. This information is collected from original articles in the literature or from the proceedings of Human Gene Mapping and Single Chromosome Workshops.
The ALIS Project in JST encourages large-scale DNA sequencing Projects in Japan. Sequencing data carried out by this projects is available here.
The international organization of scientists involved in the Human Genome Project (HGP), the global initiative to map and sequence the human genome.
Information and database on the genome mapping project of chromosome 7, at the Hospital of Sick Children.
This resource enables the collaboration of investigators and dissemination of information relevant to chromosome 9.
A human cDNA database achieved through a large-scale human cDNA analysis project.
Integrates research results from international human gene research projects, including research at TIGR. The Index is an outgrowth of our Human cDNA Database (HCD) and Expressed Gene Anatomy Database (EGAD) projects. All data in the Index are fr.
Provides a central location for chromosome 21 sequence, sequence annotation, map data, and information about resources developed at the Eleanor Roosevelt Institute.
This web site mainly provides information and data on our research, sequencing and mapping of the human genome.
Directory of all human germline variable region sequences compiled from over a thousand published sequences, including those in the current releases of the Genbank and EMBL data libraries.
This form performs searches on the Acquired Chromosome Abnormality Database. Search query capabilities.
Israel's participation for the international effort of the Human Genome Project. Project information and related links.
Computed by integrating orthologs identified at the Jackson Laboratory with putative orthologs identified by sequence homology.
An integrated physical, genetic and cytogenetic map was constructed for human chromosome 16.
A compendium of polymorphisms and mutations of the human mitochondrial DNA.
The complete data, available in a biological process-oriented database, represent the molecular phenotype of the hematopoietic stem cell.
Human Genome project information, databases, goals and links to servers.
Links to maps of genes, SNP's, and related resources.
Information from the Sanger Center.
An international consortium of sequencing centres has released into the public domain the genetic code of the 33.5 million bps that comprise the euchromatic portion of human chromosome 22.
An interdisciplinary program established and administered by the National Cancer Institute to generate the information and technological tools needed to decipher the molecular anatomy of the cancer cell.
Research focuses on the hunt for genes which influence human health disorders.
Incorporation of LLNL, LANL, and LBNL's Human Genome Centers into one accessible information and chromosome data.
The purpose of this page is to provide links to useful information for those involved in chromosome 1-related projects. Currently, this includes links for Chromosome 1 Workshops; our mailing list and on-line discussion forums; a communal data pa.
An interdisciplinary program established and administered by the National Cancer Institute to generate the information and technological tools needed to decipher the molecular anatomy of the cancer cell.
The Human Genome Research Center at the University of California, Irvine (UCI) is part of the world wide Human Genome Project, an effort to map and sequence the entire human genome. The Center at UCI has developed a radiation hybrid based map fo.
Our public access database offers information (names, genetic positions, primer sequences, sizes, clones, etc.) on STS, EST, Probes, BAC, PAC and Cosmids.
Research laboratory constructs maps of the human genome.
Information on brain structure, function, disease, and related links.
Constructed by extraction and curation of sequences from GenBank to create a non-redundant set of human transcript (HT) sequences.
The chromosome 19 physical map constructed at LLNL is a high resolution, cosmid- and BAC-based map spanning the entire chromosome. The foundation of the map consists of a set of 802 cosmid contigs assembled by automated restriction fragment anal.
Algorithms, thermodynamics and databases for RNA secondary structure.
Integrated map for each human chromosome, based on data integrated from various radiation hybrid, linkage and physical mapping resources.
Mutation registry for X-linked agammaglobulinemia.
The aim of our DNA repair studies is to elucidate excision repair and other mechanisms of cellular recovery from DNA damage. Our goal is to help identify human genes that determine the pathways for repair of, and recovery from, DNA damage.
An online facility for modelling antibodies, based on the modelling algorithm AbM.
part of the Radiation Mapping Consortium that aims to generate a radiation hybrid (RH) transcript map of the human genome that positions Expressed Sequence Tags (ESTs) relative to other informative markers (e.g. microsatellites).
DNA amount in the unreplicated haploid nuclear genome of an organism is referred to as its C-value. This database gives only the 4C DNA value for taxa arranged in alphabetical order within genera.
EMD mutation database, references, and complete lisint of EMD references.
Searchable database of human cDNA clones homologous to Drosophila mutant genes.
Mapping and sequencing project by the National Human Genome Research Institute.
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