Jd. Mcpherson et al., A RADIATION HYBRID MAP OF HUMAN-CHROMOSOME-5 WITH INTEGRATION OF CYTOGENETIC, GENETIC, AND TRANSCRIPT MAPS, PCR methods and applications, 7(9), 1997, pp. 897-909
One of the major goals of the human genome project is to establish a p
hysical map of each human chromosome with a density of sequence-tagged
site (STS) markers exceeding one every 100 kb. We report here the gen
eration of a human chromosome 5-specific radiation hybrid CRH) map tha
t includes 556 markers. Of these markers, 132 loci are ordered with a
maximum likelihood ratio of >1000:1 compared with the next most likely
order. An additional 113 loci were ordered relative to these backbone
markers with a maximum likelihood ratio of >10:1 but <1000:1. Togethe
r, these 245 loci form an ordered framework map for the chromosome. Us
ing this framework, >300 more markers were localized based on two-poin
t analysis with the ordered set. On average, there are 50 markers in c
ommon with the RH map presented here and other chromosome 5 maps inclu
ded in the current whole genome cytogenetic, genetic, and physical map
s. The accuracy of all the maps is evident in that there are no more t
han two discrepancies between any one of them and these data. All of t
he maps encompassing chromosome 5 complement each other providing exce
llent STS coverage with >2200 loci combined. The chromosome 5-specific
RH map contains 20% of these independent loci. In addition, our RH ma
p contains STSs derived from clones suitable for fluorescent in situ h
ybridization, allowing alignment to the cytogenetic map. Together, the
se maps will assist in the assembly of sequence-ready contigs and will
aid in the identification of disease loci on chromosome 5 by position
al cloning and positional candidate approaches.