نتایج جستجو برای: targeted next generation sequencing

تعداد نتایج: 736956  

Journal: :genetics in the 3rd millennium 0
fatemeh ahangari zohreh fattahi mahsa fadaee raheleh vazehan ayda abolhassani elham parsimehr

hereditary ataxias are heterogeneous group of neurodegenerative disorders classified mainly into more than 40 autosomal dominant cerebellar ataxias and 50 recessive ataxias. large amount of nearly uncommon subtypes with extensive phenotypic overlap and relatively high rate of abnormal repetitive sequence expansions, such as trinucleotide repeat expansions make diagnostic genetic testing complic...

Journal: :genetics in the 3rd millennium 0
hossein najmabadi mojgan babanejad maryam beheshtian fariba ardalani hossein daghagh nooshin nikzat

hearing loss (hl) is the most common communication disorder affecting about 1/1000 births worldwide caused by environmental or genetic factors. about 30-50% is attributed to genetic factors and till now more than 85 genes have been implicated in non-syndromic hl. in iran, hl is second to intellectual disability as the most common disability, affecting 1 of every 166 persons. about 15 years ago ...

Journal: :مجله پزشکی مولکولی 0
najme ahangari mashad, ahmadabad, new hope genetic polycinic younes moradi tehran, shahid beheshti university of medical sciences

context: detection of causative pathogen is crucial for treatment strategies in most infections. molecular diagnosis as a more sensitive and specific method, has become the best option to investigate certain pathogens, mainly viruses. recent scientific and technological approaches resulted in changing the area of diagnostic microbiology. evidence acquisition: a comprehensive online search of da...

Journal: :progress in biological sciences 2014
samaneh saadat zhaleh safikhani kambiz badie mehdi sadeghi

given the importance of transcriptome analysis in various biological studies and considering thevast amount of whole transcriptome sequencing data, it seems necessary to develop analgorithm to assemble transcriptome data. in this study we propose an algorithm fortranscriptome assembly in the absence of a reference genome. first, the contiguous sequencesare generated using de bruijn graph with d...

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