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Genome Sequencing Software Available In Mexico
14 software items found
by:BioDiscovery, A Bionano Genomics Company based inEl Segundo, CALIFORNIA (USA)
As described in Chaubey et al., Journal of Molecular Diagnostics, vol. 22, No. 6 June 2020, they used 10x WGS and validated that the NxClinical algorithm detected all CNVs and AOH that were found by high-resolution SNP arrays. Figure 2. shows a small exonic deletion detected using 10x WGS with the MSR algorithm. With higher depth NGS, smaller CNVs can be detected and integrated with sequence ...
by:NRGene based inSan Diego, CALIFORNIA (USA)
All-to-all linear mapping of multiple denovo assemblies enables intra-species gene content variation exploration. A high-quality reference genome is a great starting point, yet in many plant species the genomic diversity within the species can be as high as 50% of the genomic sequence. The discovery of ...
by:Portable Medical Technology Ltd. based inKillarney, IRELAND
ONCOassist is the go-to app for oncology and haematology professionals. It offers easy access to relevant, up-to-date tools and content when and where it is needed. With the advent of genomic sequencing, combined with an aging population, and new therapies. The decision-making process for oncology/haematology HCP’s is becoming increasingly complex. ...
by:SOPHiA Genetics based inBoston, MASSACHUSETTS (USA)
Identifying patterns of genomic scarring in ovarian cancer samples. Accurate identification and reporting of Homologous Recombination Deficiency (HRD) status are critical for better patient management. SOPHiA DDM Dx HRD Solution is a CE-marked in vitro diagnostic (IVD) application leveraging low-pass Whole Genome Sequencing (WGS) and a ...
by:Ovation based inPortland, MAINE (USA)
This Ovation IBD Genomic and Clinical Linked Data sample dataset is a packaged, real-world observational cohort of 10 Inflammatory Bowel Disease (IBD) subjects. It's available at no cost for scientists interested in evaluating Ovation’s Whole Genome Sequencing and RNAseq data with up to 30x coverage. ...
by:NRGene based inSan Diego, CALIFORNIA (USA)
The cannabis haploid genome is comprised of 735 million base pairs (Mbp). It is highly heterozygous, which means most of the regions (loci) along the genome carry two dissimilar sequences (alleles). Most assembly tools generate a synthetic (haploid) genome, resulting in a sequence for cannabis that is ...
by:NRGene based inSan Diego, CALIFORNIA (USA)
Get a jump start on your breeding program even before the greenhouses are up! Identify your desired traits and create your breeding plan in silico with our ready-to-use genomics ...
Manufactured by:sci2sci UG based inBerlin, GERMANY
VectorCat is an AI-driven platform crafted to streamline the adoption of FAIR principles—Findability, Accessibility, Interoperability, and Reusability—for data management within the biotech and pharmaceutical sectors. It addresses the critical need for proper data governance by ensuring that valuable research insights, experimental outcomes, and regulatory information are not isolated ...
Manufactured by:sci2sci UG based inBerlin, GERMANY
In the biotech and pharmaceutical industries, data is one of the most valuable assets. However, without proper data management, critical research insights, experimental results and regulatory information remain siloed, inconsistent or even lost. The FAIR data principles — Findability, Accessibility, Interoperability and Reusability — provide a framework to ensure that data can be ...
Manufactured by:CENTOGENE N.V. based inRostock, GERMANY
Analyze, interpret, and report genomic variants with our decentralized diagnostic solution – no matter where you are located. CentoCloud is a cloud-based Software as a Service (SaaS) platform specifically designed for the rapid bioinformatic analysis and interpretation of Next-Generation-Sequencing (NGS) data based on CENTOGENE’s proprietary ...
by:Seven Bridges Genomics based inCharlestown, MASSACHUSETTS (USA)
The Seven Bridges Platform is a cloud-based environment for conducting bioinformatic analyses. It is a central hub for teams to store, analyze, and jointly interpret their bioinformatic data. The Platform co-locates analysis pipelines alongside the largest genomic datasets to optimize processing. It allocates storage and compute resources on demand, to meet the needs of ever-growing ...
by:Geneious, by Dotmatics based inAuckland, NEW ZEALAND
Geneious Prime makes bioinformatics accessible by transforming raw data into visualizations that make sequence analysis intuitive and ...
by:Igenbio, Inc. based inChicago, ILLINOIS (USA)
ERGO 2.0 provides a systems biology informatics toolkit centered on comparative genomics to capture, query, and visualize sequenced genomes. Using Igenbio's proprietary algorithms, and the most comprehensive genomic database integrated with the largest collection of microbial metabolic and non-metabolic pathways, ERGO™ ...
by:Ovation based inPortland, MAINE (USA)
Ovation's real-world pathogen testing and sequencing data provides the answers researchers need to understand a pathogen's potential impact on human ...