Sequence analysis of a human repetitive DNA sequence (pTRF5.6) revealed considerable homology (76%) to the alphoid consensus sequence. Genomic blots of StuI-digested human DNA, hybridized to pTRF5.6, generated a ladder of bands with each band corresponding to oligodeoxyribonucleotide of an approx. 170-bp repeat, indicating a tandemly arrayed organization of this repeat element within the genome. Genomic hybridization analyses of unrelated individuals belonging to various geographical regions of India, using this alphoid satellite probe, revealed polymorphic bands ranging between 2 and 9 kb. Along with an individual-specific band pattern, several isomorphic bands below 2 kb were also evident. There was very little of genetic variability betw...
Genetic variation at the human a-globin gene complex has only been characterised to date ...
DNA sequences of neutral nuclear autosomal loci, compared across diverse human populations, provide ...
The central goal of medical genomics is to understand the inherited basis of sequence variation that...
Sequence analysis of a human repetitive DNA sequence (pTRF5.6) revealed considerable homology (76%) ...
A approximately 400 bp HaeIII human genomic satellite DNA band was cloned into pUC18 to construct a ...
Genetic/genomic polymorphism, i.e. variations in DNA sequences are ideally assayed by direct nucleot...
The investigation of genetic variation at the DMA sequence level in Drosophila has demonstrated the ...
Alu sequences represent the largest family of short interspersed repetitive elements (SINEs) in huma...
Alu insertion can be defined as a family of repetitive element approximately 300 base pairs long, wh...
Genetic variations among humans occur both within and among populations and range from single nucleo...
Background: The entry and dispersal of modern humans is India of remains unclear and extending with ...
Several human DNAs digested with Kpn I restriction endonuclease released a 0.6-kilobase (kb) segment...
Accessible online at: www.karger.com/cgr Abstract. To test the hypothesis that Alu and L1 elements a...
Population Genetics is the study of populations using information found from genomic data which can ...
It is often taken for granted that the human species is divided in rather homogeneous groups or race...
Genetic variation at the human a-globin gene complex has only been characterised to date ...
DNA sequences of neutral nuclear autosomal loci, compared across diverse human populations, provide ...
The central goal of medical genomics is to understand the inherited basis of sequence variation that...
Sequence analysis of a human repetitive DNA sequence (pTRF5.6) revealed considerable homology (76%) ...
A approximately 400 bp HaeIII human genomic satellite DNA band was cloned into pUC18 to construct a ...
Genetic/genomic polymorphism, i.e. variations in DNA sequences are ideally assayed by direct nucleot...
The investigation of genetic variation at the DMA sequence level in Drosophila has demonstrated the ...
Alu sequences represent the largest family of short interspersed repetitive elements (SINEs) in huma...
Alu insertion can be defined as a family of repetitive element approximately 300 base pairs long, wh...
Genetic variations among humans occur both within and among populations and range from single nucleo...
Background: The entry and dispersal of modern humans is India of remains unclear and extending with ...
Several human DNAs digested with Kpn I restriction endonuclease released a 0.6-kilobase (kb) segment...
Accessible online at: www.karger.com/cgr Abstract. To test the hypothesis that Alu and L1 elements a...
Population Genetics is the study of populations using information found from genomic data which can ...
It is often taken for granted that the human species is divided in rather homogeneous groups or race...
Genetic variation at the human a-globin gene complex has only been characterised to date ...
DNA sequences of neutral nuclear autosomal loci, compared across diverse human populations, provide ...
The central goal of medical genomics is to understand the inherited basis of sequence variation that...