The CEPH consortium linkage map of human chromosome 16
Identifieur interne : 000A33 ( Istex/Curation ); précédent : 000A32; suivant : 000A34The CEPH consortium linkage map of human chromosome 16
Auteurs : H. M. Kozman [Australie] ; T. P. Keith [États-Unis] ; H. Donis-Keller [États-Unis] ; R. L. White [États-Unis] ; J. Weissenbach [France] ; M. Dean [États-Unis] ; G. Vergnaud [France] ; K. Kidd [États-Unis] ; J. Gusella [États-Unis] ; N. J. Royle [Royaume-Uni] ; G. R. Sutherland [Australie] ; J. C. MulleySource :
- Genomics [ 0888-7543 ] ; 1995.
Descripteurs français
- Wicri :
- topic : Consortium, Base de données, Génétique.
English descriptors
- KwdEn :
- Average heterozygosity, Bglii, Buetow, Callen, Cell genet, Centromere, Ceph, Ceph consortium, Ceph consortium linkage, Ceph database, Ceph families, Ceph reference panel, Chromosome, Connell, Consortium, Consortium maps, Database, Disease genes, Double recombination event, Female maps, Female recombination, Framework markers, Genet, Genetic, Genetic distance, Genetic length, Genetic linkage, Genetic maps, Genetics, Genome, Genomics, Genotype, Heterozygosity, Hincii, Human chromosome, Human genome, Index markers, Kozman, Lalouel, Lathrop, Linkage, Linkage maps, Locus, Mapping group, Marker, Marker order, Median distance, Microsatellite, Microsatellite markers, Mspi, Mulley, Nature genet, Polymorphisme humain, Psti, Recombination, Recombination rates, Shen, Somatic cell, Taqi, Total length, Weissenbach.
- Teeft :
- Average heterozygosity, Bglii, Buetow, Callen, Cell genet, Centromere, Ceph, Ceph consortium, Ceph consortium linkage, Ceph database, Ceph families, Ceph reference panel, Chromosome, Connell, Consortium, Consortium maps, Database, Disease genes, Double recombination event, Female maps, Female recombination, Framework markers, Genet, Genetic, Genetic distance, Genetic length, Genetic linkage, Genetic maps, Genetics, Genome, Genomics, Genotype, Heterozygosity, Hincii, Human chromosome, Human genome, Index markers, Kozman, Lalouel, Lathrop, Linkage, Linkage maps, Locus, Mapping group, Marker, Marker order, Median distance, Microsatellite, Microsatellite markers, Mspi, Mulley, Nature genet, Polymorphisme humain, Psti, Recombination, Recombination rates, Shen, Somatic cell, Taqi, Total length, Weissenbach.
Abstract
Abstract: A Centre d'Etude du Polymorphisme Humain (CEPH) consortium map of human chromosome 16 has been constructed. The map contains 158 loci defined by 191 different probe/restriction enzyme combinations or primer pairs. The marker genotypes, contributed by 9 collaborating laboratories, originated from the CEPH families DNA. A total of 60 loci, with an average heterozygosity of 68%, have been placed on the framework genetic map. The genetic map contains 7 genes. The length of the sex-averaged map is 165 cM, with a mean genetic distance between loci of 2.8 cM; the median distance between markers is 2.0 cM. The male map length is 136 cM, and the female map length is 197 cM. The map covers virtually the entire chromosome, from D16S85, within 170 to 430 kb of the 16p telomere, to D16S303 at 16qter. The markers included in the linkage map have been physically mapped on a partial human chromosome 16 somatic cell hybrid panel, thus anchoring the genetic map to the cytogenetic-based physical map.
Url:
DOI: 10.1016/0888-7543(95)80108-X
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J. C. Mulley<affiliation><mods:affiliation>Centre for Medical Genetics, Department of Cytogenetics and Molecular Genetics, Women's and Children's Hospital, North Adelaide, South Australia, Australia 5006</mods:affiliation><wicri:noCountry code="subField">5006</wicri:noCountry></affiliation>Le document en format XML
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Fax: 61-8-204-7342.</wicri:noCountry></affiliation><affiliation><mods:affiliation>Centre for Medical Genetics, Department of Cytogenetics and Molecular Genetics, Women's and Children's Hospital, North Adelaide, South Australia, Australia 5006</mods:affiliation><wicri:noCountry code="subField">5006</wicri:noCountry></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:37BBBCDA26581F58583EBB4F8F1D346D7A07BD02</idno><date when="1995" year="1995">1995</date><idno type="doi">10.1016/0888-7543(95)80108-X</idno><idno type="url">https://api.istex.fr/document/37BBBCDA26581F58583EBB4F8F1D346D7A07BD02/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">000A33</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">000A33</idno><idno type="wicri:Area/Istex/Curation">000A33</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a">The CEPH consortium linkage map of human chromosome 16</title><author><name sortKey="Kozman, H M" sort="Kozman, H M" uniqKey="Kozman H" first="H. M." last="Kozman">H. M. Kozman</name><affiliation><mods:affiliation>Centre for Medical Genetics, Department of Cytogenetics and Molecular Genetics, Women's and Children's Hospital, North Adelaide, South Australia, Australia 5006</mods:affiliation></affiliation><affiliation wicri:level="1"><mods:affiliation>Department of Paediatrics, University of Adelaide, Adelaide, South Australia, Australia</mods:affiliation><country xml:lang="fr">Australie</country><wicri:regionArea>Department of Paediatrics, University of Adelaide, Adelaide, South Australia</wicri:regionArea></affiliation></author><author><name sortKey="Keith, T P" sort="Keith, T P" uniqKey="Keith T" first="T. P." last="Keith">T. P. 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Royle</name><affiliation wicri:level="1"><mods:affiliation>Department of Genetics, University of Leicester, Leicester, United Kingdom</mods:affiliation><country xml:lang="fr">Royaume-Uni</country><wicri:regionArea>Department of Genetics, University of Leicester, Leicester</wicri:regionArea></affiliation></author><author><name sortKey="Sutherland, G R" sort="Sutherland, G R" uniqKey="Sutherland G" first="G. R." last="Sutherland">G. R. Sutherland</name><affiliation><mods:affiliation>Centre for Medical Genetics, Department of Cytogenetics and Molecular Genetics, Women's and Children's Hospital, North Adelaide, South Australia, Australia 5006</mods:affiliation></affiliation><affiliation wicri:level="1"><mods:affiliation>Department of Paediatrics, University of Adelaide, Adelaide, South Australia, Australia</mods:affiliation><country xml:lang="fr">Australie</country><wicri:regionArea>Department of Paediatrics, University of Adelaide, Adelaide, South Australia</wicri:regionArea></affiliation></author><author><name sortKey="Mulley, J C" sort="Mulley, J C" uniqKey="Mulley J" first="J. C." last="Mulley">J. C. Mulley</name><affiliation><mods:affiliation>To whom correspondence should be addressed. Fax: 61-8-204-7342.</mods:affiliation></affiliation><affiliation><mods:affiliation>Centre for Medical Genetics, Department of Cytogenetics and Molecular Genetics, Women's and Children's Hospital, North Adelaide, South Australia, Australia 5006</mods:affiliation><wicri:noCountry code="subField">5006</wicri:noCountry></affiliation></author></analytic><monogr></monogr><series><title level="j">Genomics</title><title level="j" type="abbrev">YGENO</title><idno type="ISSN">0888-7543</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1995">1995</date><biblScope unit="volume">25</biblScope><biblScope unit="issue">1</biblScope><biblScope unit="page" from="44">44</biblScope><biblScope unit="page" to="58">58</biblScope></imprint><idno type="ISSN">0888-7543</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0888-7543</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Average heterozygosity</term><term>Bglii</term><term>Buetow</term><term>Callen</term><term>Cell genet</term><term>Centromere</term><term>Ceph</term><term>Ceph consortium</term><term>Ceph consortium linkage</term><term>Ceph database</term><term>Ceph families</term><term>Ceph reference panel</term><term>Chromosome</term><term>Connell</term><term>Consortium</term><term>Consortium maps</term><term>Database</term><term>Disease genes</term><term>Double recombination event</term><term>Female maps</term><term>Female recombination</term><term>Framework markers</term><term>Genet</term><term>Genetic</term><term>Genetic distance</term><term>Genetic length</term><term>Genetic linkage</term><term>Genetic maps</term><term>Genetics</term><term>Genome</term><term>Genomics</term><term>Genotype</term><term>Heterozygosity</term><term>Hincii</term><term>Human chromosome</term><term>Human genome</term><term>Index markers</term><term>Kozman</term><term>Lalouel</term><term>Lathrop</term><term>Linkage</term><term>Linkage maps</term><term>Locus</term><term>Mapping group</term><term>Marker</term><term>Marker order</term><term>Median distance</term><term>Microsatellite</term><term>Microsatellite markers</term><term>Mspi</term><term>Mulley</term><term>Nature genet</term><term>Polymorphisme humain</term><term>Psti</term><term>Recombination</term><term>Recombination rates</term><term>Shen</term><term>Somatic cell</term><term>Taqi</term><term>Total length</term><term>Weissenbach</term></keywords><keywords scheme="Teeft" xml:lang="en"><term>Average heterozygosity</term><term>Bglii</term><term>Buetow</term><term>Callen</term><term>Cell genet</term><term>Centromere</term><term>Ceph</term><term>Ceph consortium</term><term>Ceph consortium linkage</term><term>Ceph database</term><term>Ceph families</term><term>Ceph reference panel</term><term>Chromosome</term><term>Connell</term><term>Consortium</term><term>Consortium maps</term><term>Database</term><term>Disease genes</term><term>Double recombination event</term><term>Female maps</term><term>Female recombination</term><term>Framework markers</term><term>Genet</term><term>Genetic</term><term>Genetic distance</term><term>Genetic length</term><term>Genetic linkage</term><term>Genetic maps</term><term>Genetics</term><term>Genome</term><term>Genomics</term><term>Genotype</term><term>Heterozygosity</term><term>Hincii</term><term>Human chromosome</term><term>Human genome</term><term>Index markers</term><term>Kozman</term><term>Lalouel</term><term>Lathrop</term><term>Linkage</term><term>Linkage maps</term><term>Locus</term><term>Mapping group</term><term>Marker</term><term>Marker order</term><term>Median distance</term><term>Microsatellite</term><term>Microsatellite markers</term><term>Mspi</term><term>Mulley</term><term>Nature genet</term><term>Polymorphisme humain</term><term>Psti</term><term>Recombination</term><term>Recombination rates</term><term>Shen</term><term>Somatic cell</term><term>Taqi</term><term>Total length</term><term>Weissenbach</term></keywords><keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Consortium</term><term>Base de données</term><term>Génétique</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Abstract: A Centre d'Etude du Polymorphisme Humain (CEPH) consortium map of human chromosome 16 has been constructed. The map contains 158 loci defined by 191 different probe/restriction enzyme combinations or primer pairs. The marker genotypes, contributed by 9 collaborating laboratories, originated from the CEPH families DNA. A total of 60 loci, with an average heterozygosity of 68%, have been placed on the framework genetic map. The genetic map contains 7 genes. The length of the sex-averaged map is 165 cM, with a mean genetic distance between loci of 2.8 cM; the median distance between markers is 2.0 cM. The male map length is 136 cM, and the female map length is 197 cM. The map covers virtually the entire chromosome, from D16S85, within 170 to 430 kb of the 16p telomere, to D16S303 at 16qter. The markers included in the linkage map have been physically mapped on a partial human chromosome 16 somatic cell hybrid panel, thus anchoring the genetic map to the cytogenetic-based physical map.</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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