bioinformatics Downloads
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The related term ''proteomics'' was originally coined by Marc Wilkins and colleagues and is now widely identified as one of the omics- the set of post-genomic technologies which seek to further understand the genome in the molecules it encodes, their functions, interactions and connected properties. https://www.creative-proteomics.com/services/bioinformatics-for-proteomics.htm ...
Creative Proteomics' experts have extensive experience in lipidomics and bioinformatics analysis, assisting you in screening differential metabolites, identifying unknown lipid molecules, and qualitatively and quantitatively analyzing target compounds. ...
Using bioinformatics, a large amount of information on molecular biology can be organized to provide standardized data and used by researchers worldwide to design tools for the analysis of these data and to give an accurate and meaningful interpretation of the information. ...
Untargeted lipidomics uses LC-MS and GC-MS technologies to unbiasedly detect the dynamic changes of all lipid molecules before and after the stimulation or disturbance in cells, tissues, organs, or organisms. https://www.creative-proteomics.com/services/lipidomics-profiling.htm ...
Untargeted lipidomics uses LC-MS and GC-MS technologies to unbiasedly detect the dynamic changes of all lipid molecules before and after the stimulation or disturbance in cells, tissues, organs, or organisms. https://www.creative-proteomics.com/services/lipidomics-profiling.htm ...
In the current post-genome era, bioinformatics has become an important method for biological research. Due to the high frequency of variation in microbial genes, the polymorphism of microbes is a challenging yet popular topic in microbial research, especially the research on pathogenic microorganisms. ...
With years of developing and refining our bioinformatics analysis system, Creative Proteomics offers comprehensive bioinformatics support to our clients’ research! ...
Using functional genomics BT+IT (high-throughput gene sequencing technology, biological information technology, high-performance biological cloud computing technology) technology, we provide customers with comprehensive data analysis services with regard to next-generation and third-generation high-throughput sequencing outputs. ...
CD Genomics is a biotech enterprise. Using functional genomics BT+IT (high-throughput gene sequencing technology, biological information technology, high performance biological cloud computing technology) technology, we provide customers with comprehensive data analysis services with regard to next-generation and third-generation high-throughput sequencing outputs. ...
CD Genomics is a preeminent service provider specializing in sequencing and bioinformatics analysis. We provide comprehensive services with accuracy and supreme data quality based on cutting-edge platforms. Our bioinformatics analysis platform provides novel solutions for data-driven innovation to discover the hidden potential in biological data, tapping new insights into life science research ...
CD Genomics has delivered numerous sequencing projects for pharmaceutical, biotech companies, academic institutions, and government agencies. We share our knowledge in sequencing and apply it to disease research, microbiology, food and agriculture, biomarkers, drug discovery, etc. ...
CD Genomics is a preeminent service provider specializing in exosome RNA sequencing and bioinformatics analysis. Based on cutting-edge platforms, we deliver end-to-end services with more usable reads from low-input RNA and in-depth scientific and technical support. https://rna.cd-genomics.com/exosomal-long-rna-seq.html ...
Sequencing technology has advanced successfully to become one of the most used routine tools for life science research. Not only can it provide a wealth of valuable information, but when combined with other research methods, sequencing can also supply massive information. Sometimes, even with just sequencing and biomarker analysis alone, scientists can also discover biomarkers in cancer. ...
Next-gen pathway analysis using Advaita’s proprietary “Impact Analysis” method to identify significant pathways without all the noise found in other approaches. iPathwayGuide provides publication-ready results in minutes. ...
NextGENe software is the perfect analytical partner for the analysis of desktop sequencing data produced by Illumina® iSeq, Miniseq, MiSeq, NextSeq, HiSeq, and NovaSeq systems, Ion Torrent Ion GeneStudio S5, PGM, and Proton systems as well as other platforms. NextGENe software runs on a Windows® Operating System, which provides a biologist-friendly ‘point & click’ ...
CD Genomics aims at providing the research community with Illumina, PacBio SMRT and Nanopore platforms, and bioinformatics services. The utilization of real-time, long-read sequencing overcomes the challenges associated with traditional short-read sequencing technologies, to fully characterize microbial genomes - sheds new light on microbial evolution, pathogenicity, and antimicrobial resistance. ...
Sequencing technologies, genomics,and bioinformatics are rapid and effective tools to study phage genomics. In addition, further analysis,including transcription,translation, regulation, and modification, is also emerging as a technique that is extremely helpful in exploring the life cycle, specificity, lytic ability, and lysogenicity of phages. ...
NZYTech kit for Dengue subtypes is designed for the in vitro differentiation of Dengue subtypes. The kit is designed to have the broadest detection profile possible whilst remaining specific to the individual Dengue subtypes. The primers and probe sequences in this kit have 100% homology with a broad range of clinically relevant reference sequences based on a comprehensive bioinformatics ...
Enabling molecular laboratories to maximize the utility of Illumina’s TSO500 pane. SOPHiA DDM™ for TSO500 is a fully integrated bioinformatic workflow (FASTQ to Report) for Illumina TruSight™ Oncology 500 panel (TSO500). The SOPHiA DDM™ Platform combines analytical performance with streamlined interpretation of complex genomic variants in the context of comprehensive ...