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Genome Structural Articles & Analysis

27 articles found

Breaking Through Digestion Barriers with SuperCut Restriction Enzymes   

Breaking Through Digestion Barriers with SuperCut Restriction Enzymes  

Alternatively, SuperCut restriction enzymes in the Creative Enzymes portfolio include engineered variants with enhanced activity on methylated substrates for certain recognition sequences. Secondary Structure Formation Genomic regions with high GC content or repetitive sequences frequently form stable secondary structures that physically block ...

ByCreative Enzymes


Fosmid Library Construction: A Comprehensive Overview

Fosmid Library Construction: A Comprehensive Overview

Fosmid libraries represent a pivotal advancement in the field of genomics and molecular biology, offering a robust method for genomic cloning and analysis. ...

ByCreative Biogene


A Comprehensive Comparison of Illumina and Nanopore Sequencing Technologies   

A Comprehensive Comparison of Illumina and Nanopore Sequencing Technologies  

In the rapidly evolving field of genomics, sequencing technologies play a crucial role in advancing our understanding of genetic material. ...

ByCD Genomics


NGS Library Preparation Kits: A Key Component in Next-Generation Sequencing

NGS Library Preparation Kits: A Key Component in Next-Generation Sequencing

Next-Generation Sequencing (NGS) has revolutionized genomics, providing unprecedented insights into the structure and function of genomes, transcriptomes, and epigenomes. ...

ByCreative Biogene


Sequencing Depth, Coverage and Read Types for NGS   

Sequencing Depth, Coverage and Read Types for NGS  

The detailed point is to sequence the unknown genome sequence, and use bioinformatics analysis means to splice and assemble the sequence, so as to obtain the map of its genome. ...

ByCD Genomics


Amino Acid Sequence Analysis and Its Applications

Amino Acid Sequence Analysis and Its Applications

Prediction of Functional and Structural Domains Identifying known functional or structural domains using databases and tools (such as Pfam, SMART, InterPro, etc.). ...

ByMtoZ Biolabs


A Comparative Analysis of Prime Editing and CRISPR-Cas9

A Comparative Analysis of Prime Editing and CRISPR-Cas9

The Cas9 protein forms a complex with the gRNA and scans the genome to identify matching sequences. Once a match is found, the Cas9 protein binds to the DNA and induces a double-strand break. ...

ByCD Genomics


Unraveling the Mysteries of Protein Structure: The Fold Recognition Service

Unraveling the Mysteries of Protein Structure: The Fold Recognition Service

Unraveling the mysteries of protein structure has been a central focus of biological research for decades. ...

ByCD ComputaBio


Karyotype Analysis for Rare Disease

Karyotype Analysis for Rare Disease

Many rare diseases have obvious manifestations of chromosomal structural abnormalities, making it a strategy to determine the cause of diseases from a macroscopic perspective of genetics. ...

ByProtheragen


Applications of Peptide Nucleic Acid (PNA)

Applications of Peptide Nucleic Acid (PNA)

Neubase, in partnership with a global healthcare company, plans to create PNAs designed to edit genetic mutations in three undisclosed diseases. Aberrant nucleic acid structures are key to endogenous repair, which may occur under sequence-specific conditions. ...

ByBOC Sciences


Comparison Between Illumina and Nanopore Sequencing Technologies

Comparison Between Illumina and Nanopore Sequencing Technologies

Illumina sequencing is a second-generation sequencing technology that has become a powerful tool for genomics research. The method uses reversible dye terminator technology to detect the sequence of a DNA molecule. ...

ByCD Genomics


The Molecular Microbiology of SARS-CoV-2: Detection Methods and Infection Mechanism

The Molecular Microbiology of SARS-CoV-2: Detection Methods and Infection Mechanism

HCoVs are categorized into four genera depending on sequence comparisons of viral genomes: alpha, beta, gamma, and delta coronaviruses. SARS-CoV-2 is a genetically linked beta coronavirus of another bat coronavirus named BatCoV RaTG13 and SARS-CoV-1. ...

ByCD Genomics


Pan-Genome Analysis: Overview, Workflow, Application and Recent Advances

Pan-Genome Analysis: Overview, Workflow, Application and Recent Advances

What is pan-genome? A pan-genome is the sum of all genomic information within a species. With the development of genomic technology, researchers have found that a single reference genome can no longer meet the needs of genomic data analysis, and more and more species, including the human ...

ByCD Genomics


The Methods of Whole Genome Sequencing

The Methods of Whole Genome Sequencing

Overview of Whole Genome Sequencing The genome of each individual organism contains its entire genetic information. ...

ByCD Genomics


Study on Partial Glycoprotein of Feline Herpesvirus Type 1

Study on Partial Glycoprotein of Feline Herpesvirus Type 1

In addition to often invading the respiratory system, it can also infringe on the reproductive system, nervous system, conjunctiva and embryos. FHV-1 Genome Structure and Encoded Glycoproteins FHV-1 is a double-stranded DNA virus with an envelope. The full genome sequence is 126-134 kbp, and the GC content in the base is about 50%. Its ...

ByCreative Diagnostics


Applications of Microbial Whole Genome Sequencing

Applications of Microbial Whole Genome Sequencing

They are generally divided into fungi, actinomycetes, bacteria, spirulina, rickettsia, chlamydia, mycoplasma and viruses. Microbial whole genome sequencing is an important tool for mapping genomes of novel organisms, finishing genomes of known organisms, or comparing genomes across multiple samples. Sequencing the entire ...

ByCD Genomics


Long Read Sequencing Helps HLA Typing

Long Read Sequencing Helps HLA Typing

Based on long-read sequencing technology, whole human genome sequencing can accurately develop the genetic variation of DNA sequences between samples and reference genome or between individuals, such as structural variation (SV) and copy number variation (CNV), by using the obtained 10~20kb long reads to compare with the reference ...

ByCD Genomics


Long Read Sequencing Fills in the Missing Pieces of Genomics

Long Read Sequencing Fills in the Missing Pieces of Genomics

Long read sequencing has great application in the direction of de novo genome sequencing and resequencing, especially to improve the accuracy of detecting repeat regions, structural variants, as well as complex regions. Researchers used long read sequencing to produce haploid human genome assembly, populating multiple gaps in the reference ...

ByCD Genomics


Using AI to Fight a Pandemic: Insilico Medicine Announces Novel Preclinical Candidate for COVID-19 Treatment

Using AI to Fight a Pandemic: Insilico Medicine Announces Novel Preclinical Candidate for COVID-19 Treatment

There is an insightful technical report by Innophore, summarizing information about the coronavirus: its structure, active sites, sequence data, and so on. While showing similarities to beta coronaviruses found in bats, the specific coronavirus behind the COVID-19 pandemic is genetically different from other coronaviruses such as the previously known Middle East respiratory ...

ByInsilico Medicine


Genome Biology: Revealing the Genetic Structure of Seed Coat Content in Brassica Napus

Genome Biology: Revealing the Genetic Structure of Seed Coat Content in Brassica Napus

The rapeseed team at Huazhong Agricultural University, Wuhan, China, published a research paper entitled “Multi-omics analysis dissects the genetic architecture of seed coat content in Brassica napus” in Genome Biology. This study has made important progress in the analysis of the genetic basis of skin shell rate, new gene mining, and regulatory networks for seed carbon source ...

ByLifeasible

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