Results 11 to 20 of about 24,640 (259)

Whole-genome sequencing in bacteriology: state of the art

open access: yesInfection and Drug Resistance, 2013
Michael J DarkDepartment of Infectious Diseases and Pathology and Emerging Pathogens Institute, University of Florida, Gainesville, FL, USAAbstract: Over the last ten years, genome sequencing capabilities have expanded exponentially.
Dark MJ
doaj   +1 more source

Identification of optimum sequencing depth especially for de novo genome assembly of small genomes using next generation sequencing data. [PDF]

open access: yesPLoS ONE, 2013
Next Generation Sequencing (NGS) is a disruptive technology that has found widespread acceptance in the life sciences research community. The high throughput and low cost of sequencing has encouraged researchers to undertake ambitious genomic projects ...
Aarti Desai   +7 more
doaj   +1 more source

Pig genome sequence - analysis and publication strategy [PDF]

open access: yes, 2010
Background The pig genome is being sequenced and characterised under the auspices of the Swine Genome Sequencing Consortium. The sequencing strategy followed a hybrid approach combining hierarchical shotgun sequencing of BAC clones and whole genome ...
Fredholm, M.   +49 more
core   +1 more source

AFLAP: assembly-free linkage analysis pipeline using k-mers from genome sequencing data

open access: yesGenome Biology, 2021
Our assembly-free linkage analysis pipeline (AFLAP) identifies segregating markers as k-mers in the raw reads without using a reference genome assembly for calling variants and provides genotype tables for the construction of unbiased, high-density ...
Kyle Fletcher   +5 more
doaj   +1 more source

Short read Illumina data for the de novo assembly of a non-model snail species transcriptome (Radix balthica, Basommatophora, Pulmonata), and a comparison of assembler performance [PDF]

open access: yes, 2011
Background: Until recently, read lengths on the Solexa/Illumina system were too short to reliably assemble transcriptomes without a reference sequence, especially for non-model organisms.
Wheat, Christopher W.   +15 more
core   +2 more sources

Multi-Platform Next-Generation Sequencing of the Domestic Turkey (Meleagris gallopavo): Genome Assembly and Analysis [PDF]

open access: yes, 2010
A synergistic combination of two next-generation sequencing platforms with a detailed comparative BAC physical contig map provided a cost-effective assembly of the genome sequence of the domestic turkey (Meleagris gallopavo).
Kent M Reed   +394 more
core   +1 more source

In Silico Whole Genome Sequencer and Analyzer (iWGS): a Computational Pipeline to Guide the Design and Analysis of de novo Genome Sequencing Studies

open access: yesG3: Genes, Genomes, Genetics, 2016
The availability of genomes across the tree of life is highly biased toward vertebrates, pathogens, human disease models, and organisms with relatively small and simple genomes.
Xiaofan Zhou   +5 more
doaj   +1 more source

De novo assembly of a 40 Mb eukaryotic genome from short sequence reads: Sordaria macrospora, a model organism for fungal morphogenesis [PDF]

open access: yes, 2010
Filamentous fungi are of great importance in ecology, agriculture, medicine, and biotechnology. Thus, it is not surprising that genomes for more than 100 filamentous fungi have been sequenced, most of them by Sanger sequencing.
Kück Ulrich   +61 more
core   +2 more sources

Capture of complete ciliate chromosomes in single sequencing reads reveals widespread chromosome isoforms

open access: yesBMC Genomics, 2019
Background Whole-genome shotgun sequencing, which stitches together millions of short sequencing reads into a single genome, ushered in the era of modern genomics and led to a rapid expansion of the number of genome sequences available.
Kelsi A. Lindblad   +6 more
doaj   +1 more source

Long-read sequencing of the zebrafish genome reorganizes genomic architecture

open access: yesBMC Genomics, 2022
Background Nanopore sequencing technology has revolutionized the field of genome biology with its ability to generate extra-long reads that can resolve regions of the genome that were previously inaccessible to short-read sequencing platforms.
Yelena Chernyavskaya   +3 more
doaj   +1 more source

Home - About - Disclaimer - Privacy