Websites using genome sequencing as a keyword

UGENE is a free bioinformatics software for multiple sequence alignment, genome sequencing data analysis, amino acid sequence visualization

This unique research partnership is pioneering Scottish research in Human Genome discovery, to explore how our genes are involved in health and illness.

NEB is a leader in the discovery and development of molecular biology reagents. Restriction enzymes, polymerases, competent cells,sample prep for NGS, and more.

NGS Product, Next Generation Sequencing,

Amby Lab genetic laboratory

ESGI partners are focusing their efforts on integrating and standardising current and emerging technologies, and are providing access to infrastructures so that a broad group of European researchers can use the new technologies.

The Human Microbiome Project (HMP), launched by the National Institutes of Health Roadmap for Medical Research, is designed to fuel research into the human microbiome and to demonstrate correlations between changes in the microbiome and human health.

SimulConsult's decision support can be used for clinical diagnosis and for interpreting whole genome sequencing

GenomeWeb is an online news organization serving the global community of scientists, technology professionals, and executives who use and develop the latest advanced tools in molecular biology research and molecular diagnostics. Covering Genetics News, Genome, DNA, and more.

Blog about next-generation sequencing data analysis related bioinformatics issues and problems.

We are Genetics

A Revolutionary new solution for case review and reporting.The world's most comprehensive tool for genetic data analysis and management for clinical labs.

CRISPResso: Analysis of CRISPR-Cas9 genome editing outcomes from deep sequencing data

Personalis, advanced genomic services, genome services for inherited disease and cancer, precision medicine, provider of the ACE Exome, ACE Clinical Exome Test, ACE Platform, ACE Genome, is a human genome sequencing and analysis company with the most accurate and comprehensive end-to-end human exome and whole genome sequencing, analysis, and interpretation solutions and services for researchers and clinicians.

Leucine Rich Bio is a Bioinformatics driven company specializing in Genomics (NGS) Data Analysis, Interpretation and Reporting.

Michael Wendl Homepage

GeneProf is a web-based, graphical software suite for the analysis of functional genomics experiments, e.g. RNA-seq or ChIP-seq. GeneProf supports integrated analyses of RNA-seq, ChIP-seq and other data generated using next-generation sequencing platforms and provides a wealth of public data that can be easily compared with own results. This is the homepage and your gateway into the advanced data analysis functionality of the software.

State-of.the-art Whole Exome Sequencing (WES) and Whole Genome Sequencing (WGS). Turnaround time: 4 weeks, Medical Report included.

Dienstleistung DNA-Sequenzierung, Protein Sequenzierung, MALDI-TOF, Proteinidentifizierung, Thermocycler und Reinigungssysteme für DNA und RNA.

Conferenceseries.com organizing Genetics & Molecular Biology Conferences in USA, Europe, Australia and other prominent locations across the globe. We organise Genetics & Molecular Biology Meetings in the fields related to Tissue Science, Regenerative Medicine and Stem Cell Research.

Macrogen Corp. offers whole exome, genome & gene sequencing, with next gen sequencing technology, for accurate clinical diagnostics.

diArk is a database driven web application that is designed to store, organize, and present the most relevant information about completed genome projects and EST/cDNA data from eukaryotes.

GenomOncology clinical sequencing solutions translate and analyze next generation sequencing data for clinicians and cancer genome researchers.

Enlis Genomics creates software for the analysis of genome data, exome, and targeted sequencing. Variant analysis. DNA variation. Annotation. NGS analysis.

This is the website for Kai Wang Genomics and Bioinformatics Lab at Columbia.

NSilico is the provider of the world's most easy-to-use data management and analytics software for the lifesciences and healthcare industries. The company's offerings are based upon a unique and unrivalled blend of biological, computing, software-development and clinical experience and expertise which enables us to provide our customers with solutions which significantly increase the efficiency and accuracy of their work.

GenomeWeb is an online news organization serving the global community of scientists, technology professionals, and executives who use and develop the latest advanced tools in molecular biology research and molecular diagnostics. Covering Genetics News, Genome, DNA, and more.

Mendelics is a diagnostics lab focused on next-generation sequencing and analysis. We perform exome and genome sequencing for inherited diseases.

Curoverse helps you manage, process, and share massive<br /> biomedical data sets for everything from genomics to imaging.

Research Interests Key words: de novo genes, non-exonic translations, proteogenomics, phylogenomics, systems biology, evolution, sORFs, protein signaling, and big data My lab is interested in interpreting the functional effects of disease variants in (a) protein signaling, and (b) the non-coding regions of the genome.  We use - Whole Genome Sequencing, Transcriptomics, and Proteomics - 'Big…

Hi-teconline's sequencing and array technologies fuel advancements in life science research, translational and consumer genomics, and molecular diagnostics.

The Largest Ag-Genomics Meeting in the World.

Gail Taylor’s research group, based at the University of Southampton in south UK, specialises in research relating to plants and environmental change. Key plants worked on are SRC (short-rotation coppice) poplar (Populus) and willow (Salix), as well as Miscanthus, lettuce and watercress. Key research areas include the development of land use models for growing sustainable bioenergy crops, the study of GHG (greenhouse gas) balance in field sites, carbon footprint of crops grown for biofuels, QTL (quantitative trait loci) mapping in poplar for improved yield traits for use in bioenergy, carbon balance of UK bioenergy systems and re-sequencing the black poplar genome using ILLUMINA technology.

The Smith Family Clinic for Genomic Medicine has been established to use whole genome sequencing to diagnose rare, undiagnosed and misdiagnosed disease.

Provides as introduction and entry point for Alternative Expression Analysis (ALEXA) resources developed at the BC Genome Sciences Center of the BC Cancer Agency. Created by Malachi Griffith and Marco A. Marra