نتایج جستجو برای: direct genotyping
تعداد نتایج: 447487 فیلتر نتایج به سال:
Hepatitis C virus (HCV) is a major global health problem and one of the most common causes of chronic liver diseases. The current study was carried out to investigate the ability of High Resolution Melting (HRM) method in HCV genotyping. 40 HCV-Positive sera with unknown and 12 sera with known HCV genotypes were collected from different clinical laboratories in Tehran as well as Rasht in north ...
Recent advances in the engineering of sequence-specific synthetic nucleases provide enormous opportunities for genetic manipulation of gene expression in order to study their cellular function in vivo. However, current genotyping methods to detect these programmable nuclease-induced insertion/deletion (indel) mutations in targeted human cells are not compatible for high-throughput screening of ...
hepatitis c virus (hcv) is a major global health problem and one of the most common causes of chronic liver diseases. the current study was carried out to investigate the ability of high resolution melting (hrm) method in hcv genotyping. 40 hcv-positive sera with unknown and 12 sera with known hcv genotypes were collected from different clinical laboratories in tehran as well as rasht in north ...
چکیده: مول هیداتیفورم یک حاملگی غیر طبیعی انسانی است که طبق ویژگی های هیستولوژیک، ژنتیک، سونوگرافی و کلینیکی به صورت مول هیداتیفورم کامل (chm) و مول هیداتیفورم ناقص (phm) دسته بندی می شود. تمایز قایل شدن بین chm و phm با استفاده از نشانه های هیستولوژیک به تنهایی مشکل است، مول کامل رایج ترین فرم برای تبدیل شدن به کوریوکارسینوما می باشد و مول هتروزیگوت این استعداد را افزایش می دهد. ژن nlrp7 با م...
We develop expressions for the power to detect associations between parental genotypes and offspring phenotypes for quantitative traits. Three different "indirect" experimental designs are considered: full-sib, half-sib, and full-sib-half-sib families. We compare the power of these designs to detect genotype-phenotype associations relative to the common, "direct," approach of genotyping and phe...
PURPOSE The purpose of this study was to test the ability of the genotyping microarray for Usher syndrome (USH) to identify the mutations responsible for the disease in a cohort of 183 patients with USH. METHODS DNA from 183 patients with Usher syndrome from the Spanish population was analyzed using a genotyping microarray containing 429 previously identified disease-associated variants in ei...
Abstract Genotyping by sequencing (GBS) and single nucleotide polymorphism (SNP) chip technologies are the primary SNP genotyping used today. However, these have some drawbacks that limit their usefulness in analysis. We developed a robust protocol called multiplexed (GMS) using markers, providing informative genotypic data with greater flexibility. The genotypes derived from direct sequence re...
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