TY - JOUR
T1 - Construction of Representative NotI Linking Libraries Specific for the Total Human Genome and for Human Chromosome 3
AU - Zabarovsky, Eugene R.
AU - Allikmets, Rando
AU - Kholodnyuk, Irina
AU - Zabarovska, Veronika I.
AU - Paulsson, Niklas
AU - Bannikov, Vladimir M.
AU - Kashuba, Vladimir I.
AU - Dean, Michael
AU - Kisselev, Lev L.
AU - Klein, George
N1 - Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 1994/3/15
Y1 - 1994/3/15
N2 - NotI linking clones represent valuable tools for both physical and genetic mapping. Using procedures that we have previously described, several chromosome 3-specific NotI linking libraries have been constructed. Here, we describe the construction of six independent NotI linking libraries specific for the total human genome. These libraries were made using three different vectors and two combinations of restriction enzymes. Altogether, these six libraries contain more than 1 million recombinant phages. Considering that the human genome contains about 3000-5000 NotI sites, it is likely that all clonable NotI sites are present in these libraries. Two of the six libraries were transferred into plasmid form. At the same time, a chromosome 3-specific EcoRI-NotI library (NRL1) was constructed. This library considerably increases the representation of cloned NotI sites in combination with previously constructed libraries that were made using Bam HI-NotI digestion. All libraries are available on request.
AB - NotI linking clones represent valuable tools for both physical and genetic mapping. Using procedures that we have previously described, several chromosome 3-specific NotI linking libraries have been constructed. Here, we describe the construction of six independent NotI linking libraries specific for the total human genome. These libraries were made using three different vectors and two combinations of restriction enzymes. Altogether, these six libraries contain more than 1 million recombinant phages. Considering that the human genome contains about 3000-5000 NotI sites, it is likely that all clonable NotI sites are present in these libraries. Two of the six libraries were transferred into plasmid form. At the same time, a chromosome 3-specific EcoRI-NotI library (NRL1) was constructed. This library considerably increases the representation of cloned NotI sites in combination with previously constructed libraries that were made using Bam HI-NotI digestion. All libraries are available on request.
UR - http://www.scopus.com/inward/record.url?scp=0028331515&partnerID=8YFLogxK
U2 - 10.1006/geno.1994.1175
DO - 10.1006/geno.1994.1175
M3 - Article
C2 - 8020985
AN - SCOPUS:0028331515
SN - 0888-7543
VL - 20
SP - 312
EP - 316
JO - Genomics
JF - Genomics
IS - 2
ER -