» Articles » PMID: 8054980

Integrated Human Genome-wide Maps Constructed Using the CEPH Reference Panel

Overview
Journal Nat Genet
Specialty Genetics
Date 1994 Apr 1
PMID 8054980
Citations 45
Authors
Affiliations
Soon will be listed here.
Abstract

High resolution linkage maps have proven to be invaluable tools in genetic investigations. We have assembled a collection of genetic maps constructed from primary data collected from investigators performing genotyping using the Centre Etude Polymorphism Humain (CEPH) reference pedigree panel. These maps were constructed using a rigorous, semi-automated map construction algorithm that evaluates the integrity of the maps during construction. Two classes of maps were produced: a high confidence "skeletal" set composed of 544 PCR based markers, and a more highly annotated "framework" set containing maps of 1,123 markers. Genetic map locations within the framework maps are provided for an additional 1,758 loci without statistically unique interval assignments.

Citing Articles

A novel homozygous p.R1105X mutation of the AP4E1 gene in twins with hereditary spastic paraplegia and mycobacterial disease.

Kong X, Bousfiha A, Rouissi A, Itan Y, Abhyankar A, Bryant V PLoS One. 2013; 8(3):e58286.

PMID: 23472171 PMC: 3589270. DOI: 10.1371/journal.pone.0058286.


Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing.

Ratnamala U, Lyle R, Rawal R, Singh R, Vishnupriya S, Himabindu P Invest Ophthalmol Vis Sci. 2011; 52(9):6814-9.

PMID: 21357393 PMC: 3176007. DOI: 10.1167/iovs.10-6815.


Optimizing the evidence for linkage by permuting marker order.

Jun G, Song Y, Iyengar S, Elston R BMC Genet. 2006; 6 Suppl 1:S61.

PMID: 16451674 PMC: 1866721. DOI: 10.1186/1471-2156-6-S1-S61.


Allelic structure and distribution of 103 STR loci in a Southern Tunisian population.

Maalej A, Rebai A, Ayadi A, Jouida J, Makni H, Ayadi H J Genet. 2004; 83(1):65-71.

PMID: 15240910 DOI: 10.1007/BF02715830.


Hot and cold spots of recombination in the human genome: the reason we should find them and how this can be achieved.

Arnheim N, Calabrese P, Nordborg M Am J Hum Genet. 2003; 73(1):5-16.

PMID: 12772086 PMC: 1180590. DOI: 10.1086/376419.