VarDict: a novel and versatile variant caller for next-generation sequencing in cancer research [PDF]
Accurate variant calling in next generation sequencing (NGS) is critical to understand cancer genomes better. Here we present VarDict, a novel and versatile variant caller for both DNA- and RNA-sequencing data.
Ahdesmaki, Miika +9 more
core +2 more sources
Optimization of DNA extraction from human urinary samples for mycobiome community profiling. [PDF]
IntroductionRecent data suggest the urinary tract hosts a microbial community of varying composition, even in the absence of infection. Culture-independent methodologies, such as next-generation sequencing of conserved ribosomal DNA sequences, provide an
Ackerman, A Lenore +8 more
core +3 more sources
High-throughput DNA sequencing to survey bacterial histidine and tyrosine decarboxylases in raw milk cheeses [PDF]
peer-reviewedBackground The aim of this study was to employ high-throughput DNA sequencing to assess the incidence of bacteria with biogenic amine (BA; histamine and tyramine) producing potential from among 10 different cheeses varieties.
Cotter, Paul D. +6 more
core +1 more source
Highly accurate long reads are crucial for realizing the potential of biodiversity genomics
Background Generating the most contiguous, accurate genome assemblies given available sequencing technologies is a long-standing challenge in genome science.
Scott Hotaling +4 more
doaj +1 more source
Summary: Genome-wide nuclear run-ons are a powerful way to determine the impact of a perturbation such as transcription factor degradation on transcriptional patterns.
Alissa D. Guarnaccia +2 more
doaj +1 more source
Complete mitochondrial genome of the freshwater prawn Palaemon capensis (Crustacea: Palaemonidae)
The complete mitogenome of Palaemon capensis is presented here. The mitogenome is 15,925 bp in length and comprises 13 protein coding genes, 2 ribosomal subunit genes, 22 transfer RNAs, and a non-coding AT-rich region.
Louisa E. Wood +3 more
doaj +1 more source
To discuss implications of information garnered through whole-genome and exome sequencing in the practice of cardiovascular medicine.Whole-genome and exome sequencing unveils medical information embedded in individual genomes and exomes, which could be incorporated into the practice of medicine for diagnostic and therapeutic gains.
openaire +2 more sources
Molecular genotyping of multi-system rare blood types in foreign blood donors based on DNA sequencing and its clinical significance [PDF]
Jianli Gong, Xianguo Xu, Jianrong Zhu
openalex +2 more sources
A new species of Xenoturbella from the western Pacific Ocean and the evolution of Xenoturbella
Background Xenoturbella is a group of marine benthic animals lacking an anus and a centralized nervous system. Molecular phylogenetic analyses group the animal together with the Acoelomorpha, forming the Xenacoelomorpha.
Hiroaki Nakano +9 more
doaj +1 more source
An Ultrahigh-throughput Microfluidic Platform for Single-cell Genome Sequencing. [PDF]
Sequencing technologies have undergone a paradigm shift from bulk to single-cell resolution in response to an evolving understanding of the role of cellular heterogeneity in biological systems.
Abate, Adam R +3 more
core +2 more sources

