نتایج جستجو برای: short tandem repeats

تعداد نتایج: 491608  

Journal: :Croatian medical journal 2001
M Prinz M Sansone

Several case examples are presented to illustrate the usefulness of Y chromosome specific human DNA markers in a forensic setting. The markers used are the tetrameric short tandem repeats (STR's) DYS19, DYS389I, DYS389II, and DYS390. The main advantage of the Y-STR approach is the ability to detect the male component in a mixture of male and female DNA. It is also useful for the determination o...

2016
Hideaki Abe Neil J. Gemmell

Short tandem repeats (STRs) or microsatellites are well-known sequence elements that may change the spacing between transcription factor binding sites (TFBSs) in promoter regions by expansion or contraction of repetitive units. Some of these mutations have the potential to contribute to phenotypic diversity by altering patterns of gene expression. To explore how repetitive sequence motifs withi...

Journal: :Journal of virology 1999
C L Davis D Field D Metzgar R Saiz P A Morin I L Smith S A Spector C Wills

We show the presence of numerous short tandem repeats in the human cytomegalovirus (HCMV) genome and assess their usefulness as molecular markers. The genome is shown to contain at least 24 microsatellite regions that exhibit length polymorphisms. Insertion-deletion polymorphisms at these short tandem repeats are common (80% of repeats examined are polymorphic among two laboratory strains and 1...

Journal: :Genome research 1997
M Rosenberg L Hui J Ma H C Nusbaum K Clark L Robinson L Dziadzio P M Swain T Keith T J Hudson L G Biesecker J Flint

Completion of genetic and physical maps requires markers from the ends (telomeres) of every human chromosome. We have searched for short tandem repeats (microsatellites) in cosmid and P1 clones and generated 661 sequence-tagged sites (STS) from the terminal 300 kb of 31 human chromosome ends. PCR assays were successfully designed for 58 microsatellites and mapped both genetically and on radiati...

Journal: :Bioinformatics 2001
Ezekiel F. Adebiyi Tao Jiang Michael Kaufmann

We study the problem of approximate non-tandem repeat extraction. Given a long subject string S of length N over a finite alphabet Sigma and a threshold D, we would like to find all short substrings of S of length P that repeat with at most D differences, i.e., insertions, deletions, and mismatches. We give a careful theoretical characterization of the set of seeds (i.e., some maximal exact rep...

Journal: :genetics in the 3rd millennium 0
abasalt hossienzadeh colagar hamid moradi firouzjah mohammad karimian

optimization of the condition for pcr-directed sequencing of microsatellites poly adenine (a) length polymorphisms is more difficult and sensitive compared with other common sequences. replication slippage may occur for polymerase enzyme during microsatellite amplification and direct sequencing of these pcr products will be challenging for heterozygote samples. so, the aim of this study is to i...

2016
AD Roses

Structural variants (SVs) include all insertions, deletions, and rearrangements in the genome, with several common types of nucleotide repeats including single sequence repeats, short tandem repeats, and insertion-deletion length variants. Polyallelic SVs provide highly informative markers for association studies with well-phenotyped cohorts. SVs can influence gene regulation by affecting epige...

2009
Pawel Zajac Christine Öberg Afshin Ahmadian

The majority of studies employing short tandem repeats (STRs) require investigation of several of these genetic markers. As such, we demonstrate the feasibility of the trinucleotide threading (TnT) approach for scalable analysis of STRs. The TnT method represents a parallel amplification alternative that addresses the obstacles associated with multiplex PCR. In this study, analysis of the STR f...

Journal: :journal of family and reproductive health 0
habib nasiri department of medical genetics, school of medicine, tehran university of medical sciences, tehran, i jila dastan iranian fetal medicine foundation, tehran, iran mohammad hasan seifi school of medicine, iran university of medical sciences, tehran, iran noori dalooi department of medical genetics, school of medicine, tehran university of medical sciences, tehran, i saeed reza ghaffari department of medical genetics, school of medicine, tehran university of medical sciences, tehran, i

objective: classic cell culture and karyotyping is routinely used for prenatal detection of different chromosomal abnormalities. molecular cytogenetic techniques have also recently been developed and used for this purpose. quantitative florescence pcr using short tandem repeat (str) markers has more potential for high throughput diagnosis. marker heterozygosity in short tandem repeats (str) is ...

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