Results 21 to 30 of about 487,550 (165)
Review on Illumina Sequencing Technology
Austin Journal of Veterinary Science & Animal Husbandry, 2022 Illumina sequencing process utilizes biochemical methods to determine the correct order of nucleotide bases in a deoxyribonucleic acid. Macromolecule using sequencing-by-synthesis and reversible dye-terminators that enable the identification of single bases are introduced into DNA strands and used to determine the series of base pairs in DNA.
Emiyu K, Lelisa K
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NxRepair: error correction in de novo sequence assembly using Nextera mate pairs [PDF]
PeerJ, 2015 Scaffolding errors and incorrect repeat disambiguation during de novo assembly can result in large scale misassemblies in draft genomes. Nextera mate pair sequencing data provide additional information to resolve assembly ambiguities during scaffolding ...
Rebecca R. Murphy +3 more
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Rnaseq: Mrna To Illumina Library [PDF]
Protocol Exchange, 2015 This protocol details the RNAseq sample preparation starting with mRNA and ending with quality control of finished libraries. This protocol was used specifically for virus mRNA samples related to ORFeome lab group.
Marcia Sanders +2 more
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Illumina But With Nanopore: Sequencing Illumina libraries at high accuracy on the ONT MinION using R2C2 [PDF]
, 2021 Abstract High-throughput short-read sequencing has taken on a central role in research and diagnostics. Hundreds of different assays exist today to take advantage of Illumina short-read sequencers, the predominant short-read sequencing technology available today.
Alexander Zee +8 more
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Analysis of Illumina Microbial Assemblies [PDF]
, 2010 Since the emerging of second generation sequencing technologies, the evaluation of different sequencing approaches and their assembly strategies for different types of genomes has become an important undertaken. Next generation sequencing technologies dramatically increase sequence throughput while decreasing cost, making them an attractive tool for ...
Clum, Alicia +6 more
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Репродуктивная эндокринология, 2017 The article contains the results of the research, which set two main goals. The first is the determination of the actual indicators of the effectiveness of noninvasive prenatal studies and the development of counseling tools about the predictability of a
P. A. Taneja +3 more
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Paragraph: a graph-based structural variant genotyper for short-read sequence data
Genome Biology, 2019 Accurate detection and genotyping of structural variations (SVs) from short-read data is a long-standing area of development in genomics research and clinical sequencing pipelines.
Sai Chen +10 more
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Genome Biology, 2020 Repeat expansions are responsible for over 40 monogenic disorders, and undoubtedly more pathogenic repeat expansions remain to be discovered. Existing methods for detecting repeat expansions in short-read sequencing data require predefined repeat ...
Egor Dolzhenko +18 more
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BFC: correcting Illumina sequencing errors [PDF]
Bioinformatics, 2015 Abstract Summary: BFC is a free, fast and easy-to-use sequencing error corrector designed for Illumina short reads. It uses a non-greedy algorithm but still maintains a speed comparable to implementations based on greedy methods. In evaluations on real data, BFC appears to correct more errors with fewer overcorrections in comparison to ...
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, 2022 Part three of the HTTM protocol. A low-cost and high-throughput Tn-seq protocol. This part cover the preparation of Illumina sequencing libraries form genomic DNA.
Antoine Champie, Amélie De Grandmaison
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