نتایج جستجو برای: short sequence repeats

تعداد نتایج: 829751  

Journal: :iranian journal of basic medical sciences 0
ali mohammad foroughmand department of genetics, faculty of science, shahid chamran university of ahvaz, ahvaz, iran maryam jari department of genetics, faculty of science, shahid chamran university of ahvaz, ahvaz, iran seyed reza kazeminezhad department of genetics, faculty of science, shahid chamran university of ahvaz, ahvaz, iran arezu abdollahi department of genetics, faculty of science, shahid chamran university of ahvaz, ahvaz, iran leila ahmadi department of genetics, faculty of science, shahid chamran university of ahvaz, ahvaz, iran maryam heidari department of genetics, faculty of science, shahid chamran university of ahvaz, ahvaz, iran

objective(s): short tandem repeat (str) loci are the most informative dna genetic markers for attempting to individualize biological material for application in paternity and forensic cases. materials and methods: blood samples were collected and the total genomic dna was extracted. the dna samples were used for genotyping vwa and tpox str loci using pcr and polyacrylamide gel electrophoresis. ...

2009
Neng-zhi Jin Zi-xian Liu Yan-jiao Qi Wen-yuan Qiu

On the basis of information theory and statistical methods, we use mutual information, ntuple entropy and conditional entropy, combined with biological characteristics, to analyze the long range correlation and short range correlation in human Y chromosome palindromes. The magnitude distribution of the long range correlation which can be reflected by the mutual information is P5>P5a>P5b (P5a an...

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...

Journal: :Genetics 1992
M A Schofield R Agbunag J H Miller

Using site-specific mutagenesis in vitro, we have constructed Escherichia coli strains that allow the detection of the inversion of an 800-bp segment in the lac region. The invertible segment is bounded by inverted repeats of either 12 or 23 bp. Inversions occurring at these inverted repeats will restore the Lac+ phenotype. Inversions can be detected at both short homologies at frequencies rang...

2014
Minh Duc Cao Edward Tasker Kai Willadsen Michael Imelfort Sailaja Vishwanathan Sridevi Sureshkumar Sureshkumar Balasubramanian Mikael Bodén

The advances of high-throughput sequencing offer an unprecedented opportunity to study genetic variation. This is challenged by the difficulty of resolving variant calls in repetitive DNA regions. We present a Bayesian method to estimate repeat-length variation from paired-end sequence read data. The method makes variant calls based on deviations in sequence fragment sizes, allowing the analysi...

2015
Giuseppe Narzisi Michael C. Schatz

Repetitive sequences are abundant in the human genome. Different classes of repetitive DNA sequences, including simple repeats, tandem repeats, segmental duplications, interspersed repeats, and other elements, collectively span more than 50% of the genome. Because repeat sequences occur in the genome at different scales they can cause various types of sequence analysis errors, including in alig...

Journal: :journal of algebraic system 0
r. khosravi department of mathematics, fasa university, p.o.box 74617-81189, fasa, iran.

in this paper the notion of rees short exact sequence for s-posets is introduced, and we investigate the conditions for which these sequences are left or right split. unlike the case for s-acts, being right split does not imply left split. furthermore, we present equivalent conditions of a right s-poset p for the functor hom(p;-) to be exact.

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