Dr. Julie R. Korenberg's comprehensive map integrates three ways of looking at the human genome, marking critical points with fluorescent signposts for rapid translation of clinical problems into genome-based solutions. The guide has significant practical applications in cancer treatment and genetic diagnosis.
SourceCedars-Sinai Medical Center·JournalGenome Research·DateNov 28, 1999
A team of scientists has developed a method to identify common human single nucleotide polymorphisms (SNPs) located in active genes. By comparing sequences from cDNA libraries across 50 individuals, they found 201 coding SNPs that could provide valuable insights into genetic differences between people.
SourceCold Spring Harbor Laboratory·JournalGenome Research·DateNov 14, 1999
Researchers have identified 109 mariner elements in the human genome, which may contribute to genetic disorders such as Charcot-Marie-Tooth disease and hereditary neuropathy. The study's findings suggest that mariner transposons could be a hotspot for genetic change and error.
SourceCold Spring Harbor Laboratory·JournalGenome Research·DateSep 27, 1999
Researchers have successfully developed and used several types of tools to analyze the fruit fly Drosophila melanogaster genome, extracting valuable information about genes and their function. The findings include a large-scale analysis of over 1,000 mutant fly strains, which identified more than 250 new genes.
SourceHoward Hughes Medical Institute·JournalGenetics·DateSep 1, 1999
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A detailed map of the human genome will require locating at least half a million genetic markers to be useful for pharmaceutical research and development. According to Dr. Leonid Kruglyak, researchers need to locate more genetic markers to stay on track when chasing down genes that influence disease susceptibility and drug response.
SourceFred Hutchinson Cancer Center·JournalNature Genetics·DateMay 31, 1999
A new color-coded chromosome mapping system devised by Julie R. Korenberg enables quick localization of known matching genes in humans using mouse DNA, greatly speeding up research into Down Syndrome and other human illnesses. The system has profound implications for the study of human diseases and the development of effective treatments.
SourceCedars-Sinai Medical Center·JournalGenome Research·DateMay 18, 1999
The international consortium has successfully completed the pilot phase and is now accelerating the large-scale effort to sequence the human genome. The goal is to produce a working draft covering at least 90 percent of human genome sequence within one year, with completion expected by 2003.
SourceWhitehead Institute for Biomedical Research·DateMar 15, 1999
The Whitehead Institute will build chip-based genome sequencing machines that can sequence 7 million DNA letters per day, reducing the cost of capital equipment by a factor of ten. The machines will be geared towards reading longer stretches of DNA, crucial for piece together overlapping fragments.
SourceWhitehead Institute for Biomedical Research·DateMar 12, 1999
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Researchers have sequenced the genome of Caenorhabditis elegans, a tiny worm with similarities to humans. The completed genome reveals over 19,000 protein-coding genes and sheds light on human biology.
SourceNIH/National Human Genome Research Institute·JournalScience·DateDec 11, 1998
The Joint Genome Institute has exceeded its goal of sequencing 20 million base pairs for fiscal year 1998 and is on track to complete the entire human genome project in five years. The JGI's advanced technologies have enabled it to reach rates of over 2.5 million base pairs per month.
SourceDOE/Lawrence Berkeley National Laboratory·DateOct 23, 1998
The E. coli genome, consisting of 4,639,221 base pairs, has been fully sequenced, revealing 1,333 known genes and 1,000 unknown functions. The completion of the genome paves the way for a similar analysis of human DNA.
SourceUniversity of Wisconsin-Madison·JournalScience·DateSep 3, 1997
The 1996-1997 Human Genome Lecture Series featured nine speakers who discussed various aspects of the human genome, including genome sequencing, comparative genomics, and genetic research in specific populations. The series aimed to provide a comprehensive understanding of the human genome and its implications for genetics research.
SourceNIH/National Human Genome Research Institute·DateJun 11, 1997
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The approved draft proclaims the set of genes determining heredity as a 'common heritage of humanity' based on recognition of inherent dignity and equal rights. The seven-chapter declaration covers research in the human genome, rights of persons concerned, and international cooperation between developed and developing countries.
Researchers at Stanford Human Genome Center developed a powerful new computer program called Mapper to map thousands of genetic markers simultaneously. This allows for high-resolution maps with better local area resolution and rapid rebuilding process.