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Applications
- Benchtop NMR spectrometer solutions for analytical NMR sector
- Bioinformatics software solutions for single cell rna-seq sector
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Advanced Sequencing Software In USA
30 software items found
Manufactured by:Magritek Ltd. based inMalvern, PENNSYLVANIA (USA)
It has been designed for hassle-free measurements, with no need to modify a lengthy list of parameters and is even suitable for non-NMR users. However, if you know your NMR and want to have a better control of experimental parameters, use more advanced sequences or even write new ones you might be interested in what Spinsolve Expert can ...
by:SOPHiA Genetics based inBoston, MASSACHUSETTS (USA)
Over the last decade, substantial progress has been made in the discovery of genetic variants influencing a range of metabolic diseases.1 The advances in next generation sequencing (NGS) technologies have contributed to elucidation of the pathogenic role of variants associated with metabolic phenotypes, leading to a significant improvement in the throughput and ...
Manufactured by:Kontur AS based inTrondheim, NORWAY
The embedded Navigation Assistant provides real-time visualization of vehicle trajectory and surveyed area. Live monitoring of GPS accuracy ensures optimal data positioning. Advanced users may customize collection ...
by:Snic Solutions based inIrving, TEXAS (USA)
Opcenter Execution drives continuous improvement in manufacturing by integrating and analyzing real-time data, enabling manufacturers to monitor and optimize operations. It identifies inefficiencies, supports corrective actions, and facilitates process refinement, reducing waste and improving product quality ...
Manufactured by:Agilent Technologies, Inc. based inSanta Clara, CALIFORNIA (USA)
The SureSelect Focused Exome is a highly targeted design that enables analysis of only the disease-associated targets providing deep coverage even on a benchtop sequencer. This design provides 20 or more reads for 95% of targets at 1.5Gb (100x) of sequencing and 98% of targets with 3Gb (200x) of sequencing enabling superior coverage of disease-associated regions even when sequenced on benchtop ...
by:Partek Incorporated based inChesterfield, MISSOURI (USA)
Partek® Flow® is a start-to-finish software analysis solution for next generation sequencing data applications. It has an easy-to-use interface, robust statistical algorithms, information-rich visualizations, and cutting-edge genomic tools enabling researchers of all skill levels to confidently perform data analysis. All the tools you need to quickly go from raw data files to meaningful ...
by:BioDiscovery, A Bionano Genomics Company based inEl Segundo, CALIFORNIA (USA)
Bionano's NxClinicalTM Software is the leading copy number variation (CNV) analysis software solution for cytogenetics and molecular laboratories. The latest software (v6.2) release adds three measures of genomic instability for homologous recombination repair deficiency (HRD) in solid tumors: Loss of heterozygosity (LOH). Telomeric Allelic Imbalance (TAI). Large-Scale State Transitions (LST). ...
by:SoftGenetics, LLC. based inState College, PENNSYLVANIA (USA)
Variant Interpretation * Variant Tracking * Coverage Confirmation Save Time & Resources * Compatible with data from all NGS systems * Targeted Panels and Whole Exome Sequencing. Developed in collaboration with the Laboratory Medicine, Information Technology, and Health Science Research departments of Mayo Clinic, Geneticist Assistant NGS Interpretative Workbench is a unique tool for the ...
by:Echelon Diagnostics based inReno, NEVADA (USA)
Through cell-free DNA testing technology, EchelonDx leverages next-generation sequencing data to provide new approaches toward improving oncology patient ...
Manufactured by:Listen Inc. based inBoston, MASSACHUSETTS (USA)
SoundCheck by Listen, Inc. is an advanced audio measurement software designed for precise testing across various applications. It offers a high level of accuracy with its robust measurement algorithms, supporting open-loop and TIA standard tests for smart devices. SoundCheck's modular software can be customized or expanded with additional modules to meet exacting specification ...
by:SOPHiA Genetics based inBoston, MASSACHUSETTS (USA)
Next-generation sequencing (NGS) of the human exome has the potential to identify pathogenic variants responsible for complex phenotypes associated with rare ...
by:SOPHiA Genetics based inBoston, MASSACHUSETTS (USA)
Next-generation sequencing (NGS) has the potential to revolutionize the diagnosis and treatment of cancers and rare diseases but creates extremely large, complex, and noisy datasets for analysis. Without the right analytical technology, pinpointing causative variants and obtaining actionable insights from NGS data requires specialist skills, multiple resources, and considerable time. The ...
by:SoftGenetics, LLC. based inState College, PENNSYLVANIA (USA)
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’ ...
by:Benchling based inSan Francisco, CALIFORNIA (USA)
Design and analyze DNA, RNA, and amino acid sequences with intelligent software that boosts throughput, drives collaborations and supports innovative ...
by:SOPHiA Genetics based inBoston, MASSACHUSETTS (USA)
Hematological tumors represent the fourth most frequent cancer type in the developed world. In addition to the continuously evolving clinical guidelines2, harnessing of all the available information when investigating hematological disorders into meaningful insights can be outdated, inaccurate, costly, and time-consuming. This ultimately risks limiting researchers’ productivity, thus ...
by:DNAnexus, Inc. based inMountain View, CALIFORNIA (USA)
DNAnexus Titan™ powers the future of genomics research and clinical pipelines with trusted, high-performance data analysis ...
by:Sapio Sciences based inBaltimore, MARYLAND (USA)
With our LIMS configurable technology and workflow templates, projects are completed in a fraction of the time and cost of standard LIMS ...
by:Seven Bridges Genomics based inCharlestown, MASSACHUSETTS (USA)
The representation of the human reference genome as a linear haploid DNA sequence poses limitations when trying to incorporate the known genetic diversity of human populations. This has led to the development of graph-based references, able to naturally represent all polymorphisms, including insertions, deletions, and structural ...
by:Qlucore AB based inLund, SWEDEN
Qlucore's clinical diagnostics solutions for multi-omics companion and precision diagnostics include AI-powered, disease-specific machine learning based classifier models and are combined with patient-friendly visualizations in a an easy-to-use and cost-effective software solution which integrates with a wide range of data generating techniques and instruments. ...
by:SOPHiA Genetics based inBoston, MASSACHUSETTS (USA)
Hereditary causes account for ∼10% of cancer cases, and an estimated 20% of cancer patients have a family history of cancer. Identification of an individual with a suspected hereditable cancer can lead to additional examinations and help formulate the most appropriate prevention strategies. Evaluating the predisposition to develop inherited cancer depends on the ability to characterize genes ...