نتایج جستجو برای: illumina hiseq 2000
تعداد نتایج: 178889 فیلتر نتایج به سال:
BACKGROUND Vibrio fluvialis is an emerging diarrheal pathogen for which no genome is currently available. In this work, draft genomes of two closely related clinical strains PG41 and I21563 have been explored. RESULTS V. fluvialis strains PG41 and I21563 were sequenced on the Illumina HiSeq 1000 platform to obtain draft genomes of 5.3 Mbp and 4.4 Mbp respectively. Our genome data reveal the p...
The type strain SUR2 of the novel species Chryseobacterium limigenitum was isolated from a dehydrated sludge of the municipal sewage treatment plant in Dogoše near Maribor in Slovenia. The draft genome, with 60 contigs, 4,697,725bp, 34.4% of G+C content, was obtained using the Illumina HiSeq 2500-1 platform. Joint Genome Institute Microbial Genome Annotation Pipeline (MGAP v.4) has identified 4...
Exome and whole-genome sequencing studies are becoming increasingly common, but little is known about the accuracy of the genotype calls made by the commonly used platforms. Here we use replicate high-coverage sequencing of blood and saliva DNA samples from four European-American individuals to estimate lower bounds on the error rates of Complete Genomics and Illumina HiSeq whole-genome and who...
Mangosteen (Garcinia mangostana L.) has exceptional potential for commercial and pharmaceutical applications due to its delicious fruit and medicinal properties. Nevertheless, the molecular mechanism of mangosteen seed development is poorly understood. In this study, we performed transcriptomic analysis of four seed developmental stages; eight, ten, twelve and fourteen weeks after anthesis. Ill...
The complete mitochondrial genome of the stone loach Barbatula barbatula (Linnaeus, 1758) (Actinopterygii: Cypriniformes: Nemacheilidae) has been sequenced using a genome-skimming approach on an Illumina Hiseq 2500 platform. The mitochondrial genome of B. barbatula was determined to be 16,630 bp long and presents an organization typical of vertebrate mitogenomes. The mean coverage was 82× with ...
Methods The exons of the NLRP3 gene were amplified via PCR from genomic PBMC DNA. The obtained PCR products were sequenced with an Illumina HiSeq platform. For SNP calling we used the GATK pipeline of the 1000 Genome Project, if the coverage attained 40,000 fold. In order to prove the accuracy of the method, we quantified dilutions of a known heterozygous mutation (T348M) mixed with wildtype DN...
In eukaryotes, nucleosomes participate in all DNA-templated events by regulating access to the underlying DNA sequence. However, nucleosome dynamics during a genome response have not been well characterized [1,2]. We stimulated Drosophila S2 cells with heat-killed Gram-negative bacteria Salmonella typhimurium, and mapped genome-wide nucleosome occupancy at high temporal resolution by MNase-seq ...
Local Sudanese sheep populations inhabiting diverse environmental conditions and holding opposing morphologies provide opportunities for molecular-genetic research. Characterizing their genome is crucial sustainable breeding improvement targeting favorable genes in programs. However, the of these populations, which comprises several subtypes, remains uncharacterized using whole-genome sequence ...
مقدمه: علت بیشتر موارد صرع ناشناخته است و عوامل ارثی می تواند در بروز آن نقش داشته باشد. امروزه، تحقیقات وسیعی در زمینه ی علل ایجاد صرع در حال انجام است. هدف از انجام این مطالعه، شناسایی ژن (های) عامل صرع غیر سندرمی با الگوی توارث اتوزومی مغلوب در یک خانواده ی ایرانی به روش توالی یابی کامل اگزوم بود. روش ها: مطالعه ی حاضر، از نوع تجربی بود. dna ژنومی از خون سه فرد مبتلا و یکی از افراد سالم خانو...
Abstract Background Next Generation Sequencing (NGS) is the fundament of various studies, providing insights into questions from biology and medicine. Nevertheless, integrating data different experimental backgrounds can introduce strong biases. In order to methodically investigate magnitude systematic errors in single nucleotide variant calls, we performed a cross-sectional observational study...
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