نتایج جستجو برای: genome sequencing for each individual was performed using next

تعداد نتایج: 12226473  

2015
Juan P. Isaza Ana Luz Galván Victor Polanco Bernice Huang Andrey V. Matveyev Myrna G. Serrano Patricio Manque Gregory A. Buck Juan F. Alzate

Cryptosporidium parvum and C. hominis are the most relevant species of this genus for human health. Both cause a self-limiting diarrhea in immunocompetent individuals, but cause potentially life-threatening disease in the immunocompromised. Despite the importance of these pathogens, only one reference genome of each has been analyzed and published. These two reference genomes were sequenced usi...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه فردوسی مشهد - دانشکده مهندسی 1389

abstract type-ii fuzzy logic has shown its superiority over traditional fuzzy logic when dealing with uncertainty. type-ii fuzzy logic controllers are however newer and more promising approaches that have been recently applied to various fields due to their significant contribution especially when the noise (as an important instance of uncertainty) emerges. during the design of type- i fuz...

Journal: :Molecular ecology 2013
Mathieu Gautier Julien Foucaud Karim Gharbi Timothée Cézard Maxime Galan Anne Loiseau Marian Thomson Pierre Pudlo Carole Kerdelhué Arnaud Estoup

Molecular markers produced by next-generation sequencing (NGS) technologies are revolutionizing genetic research. However, the costs of analysing large numbers of individual genomes remain prohibitive for most population genetics studies. Here, we present results based on mathematical derivations showing that, under many realistic experimental designs, NGS of DNA pools from diploid individuals ...

Journal: :Czech Journal of Animal Science 2021

Current animal breeding approaches are strongly associated with the development of sophisticated molecular genetics methods and techniques. Worldwide expansion genomic selection can be achieved by identification genetic DNA markers implementation microarray (“chip”) technology. Further advancement was next-generation sequencing methods, high-throughput genotyping platforms, targeted genome edit...

2014
Stephan Pabinger Andreas Dander Maria Fischer René Snajder Michael Sperk Mirjana Efremova Birgit Krabichler Michael R. Speicher Johannes Zschocke Zlatko Trajanoski

Recent advances in genome sequencing technologies provide unprecedented opportunities to characterize individual genomic landscapes and identify mutations relevant for diagnosis and therapy. Specifically, whole-exome sequencing using next-generation sequencing (NGS) technologies is gaining popularity in the human genetics community due to the moderate costs, manageable data amounts and straight...

2017
Sejoon Lee Soohyun Lee Scott Ouellette Woong-Yang Park Eunjung A. Lee Peter J. Park

In many next-generation sequencing (NGS) studies, multiple samples or data types are profiled for each individual. An important quality control (QC) step in these studies is to ensure that datasets from the same subject are properly paired. Given the heterogeneity of data types, file types and sequencing depths in a multi-dimensional study, a robust program that provides a standardized metric f...

2005
Marcel Margulies Michael Egholm William E. Altman Said Attiya Joel S. Bader Lisa A. Bemben Jan Berka Michael S. Braverman Yi-Ju Chen Zhoutao Chen Scott B. Dewell Lei Du Joseph M. Fierro Xavier V. Gomes Brian C. Goodwin Wen He Scott Helgesen Chun He Ho Gerard P. Irzyk Szilveszter C. Jando Thomas P. Jarvie Kshama B. Jirage Jong-Bum Kim James R. Knight Janna R. Lanza John H. Leamon Steven M. Lefkowitz Ming Lei Jing Li Kenton L. Lohman Hong Lu Vinod B. Makhijani Keith E. McDade Michael P. McKenna Eugene W. Myers Elizabeth Nickerson John R. Nobile Ramona Plant Bernard P. Puc Michael T. Ronan George T. Roth Gary J. Sarkis Jan Fredrik Simons John W. Simpson Maithreyan Srinivasan Karrie R. Tartaro Alexander Tomasz Kari A. Vogt Greg A. Volkmer Shally H. Wang Yong Wang Michael P. Weiner

We describe a scalable, highly parallel sequencing system with raw throughput significantly greater than that of state-of-the-art capillary electrophoresis instruments. The apparatus uses a novel 60×60 mm2 fibreoptic slide containing 1,600,000 individual wells and is able to sequence 25 million bases, at 99% or better accuracy (phred 20), in a 4 hour run. To provide sequencing templates, we clo...

Journal: :Bioinformatics 2015
Kathleen M. Fisch Tobias Meißner Louis Gioia Jean-Christophe Ducom Tristan M. Carland Salvatore Loguercio Andrew I. Su

MOTIVATION Omics Pipe (http://sulab.scripps.edu/omicspipe) is a computational framework that automates multi-omics data analysis pipelines on high performance compute clusters and in the cloud. It supports best practice published pipelines for RNA-seq, miRNA-seq, Exome-seq, Whole-Genome sequencing, ChIP-seq analyses and automatic processing of data from The Cancer Genome Atlas (TCGA). Omics Pip...

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