Greg Schuler
A5019011273- Genomics and Phylogenetic Studies
- Genomics and Chromatin Dynamics
- Genomic variations and chromosomal abnormalities
- Biomedical Text Mining and Ontologies
- Genetics, Bioinformatics, and Biomedical Research
- Gene expression and cancer classification
- Molecular Biology Techniques and Applications
- Genetic Mapping and Diversity in Plants and Animals
- RNA and protein synthesis mechanisms
- RNA Interference and Gene Delivery
- Chromosomal and Genetic Variations
- Peptidase Inhibition and Analysis
- Genomics and Rare Diseases
- Animal Genetics and Reproduction
- NF-κB Signaling Pathways
- Wound Healing and Treatments
- Genetic diversity and population structure
- Immunotherapy and Immune Responses
- Digestive system and related health
- Genetic factors in colorectal cancer
- Forensic and Genetic Research
Medical University of Graz
2010-2011
National Institutes of Health
1996-2011
National Center for Biotechnology Information
1998-2011
University of Utah
2002
Johns Hopkins University
2002
Stanford University
1999
Incyte (United States)
1999
Friedrich-Alexander-Universität Erlangen-Nürnberg
1999
The temporal program of gene expression during a model physiological response human cells, the fibroblasts to serum, was explored with complementary DNA microarray representing about 8600 different genes. Genes could be clustered into groups on basis their patterns in this program. Many features transcriptional appeared related physiology wound repair, suggesting that play larger and richer role complex multicellular than had previously been appreciated.
In addition to maintaining the GenBank(R) nucleic acid sequence database, National Center for Biotechnology Information (NCBI) provides analysis and retrieval resources data in GenBank other biological available through NCBI's web site. NCBI include Entrez, Entrez Programming Utilities, My NCBI, PubMed, PubMed Central, Gene, Taxonomy Browser, BLAST, BLAST Link, Electronic PCR, OrfFinder, Spidey, Splign, RefSeq, UniGene, HomoloGene, ProtEST, dbMHC, dbSNP, Cancer Chromosomes, Genome, Genome...
The human genome is thought to harbor 50,000 100,000 genes, of which about half have been sampled date in the form expressed sequence tags. An international consortium was organized develop and map gene-based tagged site markers on a set two radiation hybrid panels yeast artificial chromosome library. More than 16,000 genes mapped relative framework that contains 1000 polymorphic genetic markers. gene unifies existing physical maps with nucleotide protein databases fashion should speed...
In addition to maintaining the GenBank® nucleic acid sequence database, National Center for Biotechnology Information (NCBI) provides analysis and retrieval resources data in GenBank other biological made available through NCBI Web site. include Entrez, Entrez Programming Utilities, MyNCBI, PubMed, PubMed Central (PMC), Gene, Taxonomy Browser, BLAST, BLAST Link (BLink), Primer-BLAST, COBALT, Electronic PCR, OrfFinder, Splign, ProSplign, RefSeq, UniGene, HomoloGene, ProtEST, dbMHC, dbSNP,...
The National Institutes of Health's Mammalian Gene Collection (MGC) project was designed to generate and sequence a publicly accessible cDNA resource containing complete open reading frame (ORF) for every human mouse gene. initially used random strategy select clones from large number libraries diverse tissues. Candidate were chosen based on 5′-EST sequences, then fully sequenced high accuracy analyzed by algorithms developed this project. Currently, more than 11,000 10,000 genes are...
In addition to maintaining the GenBank® nucleic acid sequence database, National Center for Biotechnology Information (NCBI) provides analysis and retrieval resources data in GenBank other biological made available through NCBI Website. include Entrez, Entrez Programming Utilities, MyNCBI, PubMed, PubMed Central (PMC), Gene, Taxonomy Browser, BLAST, BLAST Link (BLink), Primer-BLAST, COBALT, Splign, RefSeq, UniGene, HomoloGene, ProtEST, dbMHC, dbSNP, dbVar, Epigenomics, Genome related tools,...
Single-nucleotide polymorphisms (SNPs) constitute the great majority of variations in human genome, and as heritable variable landmarks they are useful markers for disease mapping resolving population structure. Redundant coverage overlaps large-insert genomic clones, sequenced part Human Genome Project, comprises a quarter it is representative terms base compositional functional sequence features. We mined these regions to produce 500,000 high-confidence SNP candidates uniform resource...
The chromosomal localization of the human CD83 gene was determined using somatic cell hybrids, a radiation hybrid mapping panel and FISH analysis on metaphase chromosomes. PCR-based single chromosome identified presence 6 subsequent Genebridge4 located between AFMa192wg9 AFMb322wd1 with lod score 9.2. Finally, localized to band p23.