Results 31 to 40 of about 3,718,372 (390)

Enhanced Multi-Criteria DNA Sequence Analysis Using Neutrosophic Logic and Deep Learning: An Integrated Approach for Comparison and Classification [PDF]

open access: yesNeutrosophic Sets and Systems
This paper presents a comprehensive approach for analyzing DNA sequences and attempts to find a practical solution to the problems of comparing and classifying genomic data, which have become increasingly complex and noisy.
Romany M. Farag   +6 more
doaj   +1 more source

DNA sequence analysis of SLC26A5, encoding prestin, in a patient-control cohort: identification of fourteen novel DNA sequence variations. [PDF]

open access: yesPLoS ONE, 2009
Prestin, encoded by the gene SLC26A5, is a transmembrane protein of the cochlear outer hair cell (OHC). Prestin is required for the somatic electromotile activity of OHCs, which is absent in OHCs and causes severe hearing impairment in mice lacking ...
Jacob S Minor   +3 more
doaj   +1 more source

Copper Ions Induce DNA Sequence Variation in Zygotic Embryo Culture-Derived Barley Regenerants

open access: yesFrontiers in Plant Science, 2021
In vitro tissue culture could be exploited to study cellular mechanisms that induce sequence variation. Altering the metal ion composition of tissue culture medium affects biochemical pathways involved in tissue culture-induced variation. Copper ions are
Renata Orłowska   +2 more
doaj   +1 more source

Cloning and characterisation of the S.pombe rad15 gene, a homologue to the S.cerevisiae RAD3 and human ERCC2 genes [PDF]

open access: yes, 1992
The RAD3 gene of Saccharomyces cerevisiae encodes an ATP-dependent 5' - 3' DNA helicase, which is involved in excision repair of ultraviolet radiation damage.
Alan R. Lehmann   +6 more
core   +3 more sources

Towards precision quantification of contamination in metagenomic sequencing experiments

open access: yesMicrobiome, 2019
Metagenomic next-generation sequencing (mNGS) experiments involving small amounts of nucleic acid input are highly susceptible to erroneous conclusions resulting from unintentional sequencing of occult contaminants, especially those derived from ...
M. S. Zinter   +4 more
doaj   +1 more source

Completely mitochondrial genome of Neolissochilus heterostomus

open access: yesMitochondrial DNA. Part B. Resources, 2021
In this study, we determined the complete mitochondrial genome of Neolissochilus heterostomus. The genome is 16,585 bp in length, including 2 ribosomal RNA genes, 13 proteins-coding genes, 22 transfer RNA genes, and two non-coding control regions ...
Jinghong He   +5 more
doaj   +1 more source

Multiplexed DNA-Modified Electrodes [PDF]

open access: yes, 2010
We report the use of silicon chips with 16 DNA-modified electrodes (DME chips) utilizing DNA-mediated charge transport for multiplexed detection of DNA and DNA-binding protein targets.
Barton, Jacqueline K.   +3 more
core   +2 more sources

A Deep Learning Model for Predicting DNA N6-Methyladenine (6mA) Sites in Eukaryotes

open access: yesIEEE Access, 2020
DNA N6-methyladenine (6mA) is an epigenetic modification, which is involved in many biological regulation processes like DNA replication, DNA repair, transcription, and gene expression regulation.
Lokuthota Hewage Roland   +1 more
doaj   +1 more source

High-Throughput DNA Analysis Platform Based on an Optofluidic Ring Resonator Laser

open access: yesApplied Sciences, 2022
We demonstrate an optofluidic laser using DNA microdroplets, an intercalating dye, and a glass capillary ring resonator. Only the target DNA emits the laser signal, while the non-target DNA, including those with single-base mismatches, exhibits zero ...
Chan Seok Jun, Wonsuk Lee
doaj   +1 more source

Delimiting the Origin of a B Chromosome by FISH Mapping, Chromosome Painting and DNA Sequence Analysis in Astyanax paranae (Teleostei, Characiformes)

open access: yesPLoS ONE, 2014
Supernumerary (B) chromosomes have been shown to contain a wide variety of repetitive sequences. For this reason, fluorescent in situ hybridisation (FISH) is a useful tool for ascertaining the origin of these genomic elements, especially when combined ...
D. M. Silva   +10 more
semanticscholar   +1 more source

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