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PMID: 8188250 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

CEPH consortium Map of chromosome 9.

Genomics ·Vol. 19 ·No. 2 ·1994-01-15 ·Pages 203-14

Attwood J, Chiano M, Collins A, Donis-Keller H, Dracopoli N, Fountain J, Falk C, Goudie D, Gusella J, Haines J

Abstract

This paper describes the Centre d'Etude du Polymorphisme Humain (CEPH) consortium linkage map of chromosome 9. A total of 124 markers were typed in the CEPH family DNAs by 14 contributing laboratories; of these, 42 loci are ordered on the map with likelihood support of at least 1000:1. The uniquely placed markers include 31 that can be typed by PCR. A further 28 markers that can be typed by PCR are approximately positioned on the map. Multilocus linkage analysis with CRI-MAP has produced male, female, and sex-averaged maps extending for 176, 237, and 209 cM, respectively, while sex-averaged maps produced with MAPMAKER and the multiple two-point program MAP extended for 170 and 129 cM, respectively. The male map contains only two intervals greater than 10 cM, and the mean genetic distance between the 42 uniquely placed loci is 4.3 cM. However, no markers were available to anchor the map at either telomere or the centromere. The results confirm the high level of interference suggested by chiasma maps of chromosome 9. Detailed meiotic breakpoints for three of the families are shown. These can be used to provide rapid placement of any new marker without the need for statistical analysis.

MeSH Terms
Alleles Chromosome Mapping Chromosomes, Human, Pair 9 Female France Genetic Markers Humans Male Polymerase Chain Reaction Recombination, Genetic
Chemicals
Genetic Markers
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Attwood J
MRC Human Biochemical Genetics Unit, Galton Laboratory, University College London, England.
Chiano M
Collins A
Donis-Keller H
Dracopoli N
Fountain J
Falk C
Goudie D
Gusella J
Haines J
Article Info
Journal
Genomics
Abbr.
Genomics
ISSN
0888-7543
Published
1994-01-15
Pages
203-14
Language
English
Region
United States
NLM ID
8800135
Subset
IM
Grants
NIGMS NIH HHS · GM29177 · United States
NHGRI NIH HHS · HG00598 · United States
Wellcome Trust · United Kingdom
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