Results 11 to 20 of about 308,842 (252)

Unlocking short read sequencing for metagenomics.

open access: yesPLoS ONE, 2010
BackgroundDifferent high-throughput nucleic acid sequencing platforms are currently available but a trade-off currently exists between the cost and number of reads that can be generated versus the read length that can be achieved.Methodology/principal ...
Sébastien Rodrigue   +6 more
doaj   +6 more sources

INSurVeyor: improving insertion calling from short read sequencing data [PDF]

open access: yesNature Communications, 2023
Insertions are one of the major types of structural variations and are defined as the addition of 50 nucleotides or more into a DNA sequence. Several methods exist to detect insertions from next-generation sequencing short read data, but they generally ...
Ramesh Rajaby   +6 more
doaj   +2 more sources

Comparing genomes recovered from time-series metagenomes using long- and short-read sequencing technologies [PDF]

open access: yesMicrobiome, 2023
Background Over the past years, sequencing technologies have expanded our ability to examine novel microbial metabolisms and diversity previously obscured by isolation approaches.
Luis H. Orellana   +3 more
doaj   +2 more sources

A large-scale comparative metagenomic analysis of short-read sequencing platforms indicates high taxonomic concordance and functional analysis challenge [PDF]

open access: yesmSystems
Driven by the increasing scale of microbiome studies and the rise of large, continuously expanding population cohorts, the volume of sequencing data is growing rapidly.
Kinga Zielińska   +4 more
doaj   +2 more sources

Oxford nanopore long-read sequencing enables the generation of complete bacterial and plasmid genomes without short-read sequencing [PDF]

open access: yesFrontiers in Microbiology, 2023
IntroductionGenome-based analysis is crucial in monitoring antibiotic-resistant bacteria (ARB)and antibiotic-resistance genes (ARGs). Short-read sequencing is typically used to obtain incomplete draft genomes, while long-read sequencing can obtain ...
Wenxuan Zhao   +11 more
doaj   +2 more sources

Will long-read sequencing technologies replace short-read sequencing technologies in the next 10 years? [PDF]

open access: yesAfrican Journal of Laboratory Medicine, 2020
No abstract available.
Boluwatife A. Adewale
doaj   +2 more sources

SeqEntropy: genome-wide assessment of repeats for short read sequencing. [PDF]

open access: yesPLoS ONE, 2013
BACKGROUND: Recent studies on genome assembly from short-read sequencing data reported the limitation of this technology to reconstruct the entire genome even at very high depth coverage. We investigated the limitation from the perspective of information
Hsueh-Ting Chu   +6 more
doaj   +4 more sources

Haplotype-Phased Synthetic Long Reads from Short-Read Sequencing. [PDF]

open access: yesPLoS ONE, 2016
Next-generation DNA sequencing has revolutionized the study of biology. However, the short read lengths of the dominant instruments complicate assembly of complex genomes and haplotype phasing of mixtures of similar sequences.
James A Stapleton   +12 more
doaj   +6 more sources

Whole-genome sequencing and assembly with high-throughput, short-read technologies.

open access: yesPLoS ONE, 2007
While recently developed short-read sequencing technologies may dramatically reduce the sequencing cost and eventually achieve the $1000 goal for re-sequencing, their limitations prevent the de novo sequencing of eukaryotic genomes with the standard ...
Andreas Sundquist   +4 more
doaj   +3 more sources

Using short read sequencing to characterise balanced reciprocal translocations in pigs [PDF]

open access: yesBMC Genomics, 2020
Background A balanced constitutional reciprocal translocation (RT) is a mutual exchange of terminal segments of two non-homologous chromosomes without any loss or gain of DNA in germline cells.
Aniek C. Bouwman   +4 more
doaj   +3 more sources

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