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Undefined Software Near Madagascar
16,621 software items found
by:Molsoft LLCÂ Â based inSan Diego, CALIFORNIA (USA)
iMolview is an app for the iPhone/iPad and Android that lets you browse protein, DNA, and drug molecules in 3D. The app has a direct link to the Protein Data Bank (PDB) and DrugBank and has a fast and easy to use interface. Touching the molecules via the screen allows you to interact immediately with the 3D structures in a unique way. You can zoom in and out, rotate, spin, pan, and clip the 3D ...
by:Molsoft LLCÂ Â based inSan Diego, CALIFORNIA (USA)
The ICM-Bio provides the environment for manipulation of sequences, alignments, profiles and databases both interactively and in a batch mode. It also provides direct connectivity with 3D models and a fully interactive alignment editor and annotator.This package also contains all the features in ...
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:BioDiscovery, A Bionano Genomics Company  based inEl Segundo, CALIFORNIA (USA)
Arming researchers with advanced genomic data analysis and visualization tools. Easy-to-use software provides cutting-edge statistical tools to advance scientific ...
by:BioDiscovery, A Bionano Genomics Company  based inEl Segundo, CALIFORNIA (USA)
The most comprehensive and up-to-date solution for cytogenetics and molecular genetics in one system for analysis and interpretation of all genomic variants from microarray and NGS ...
by:BioDiscovery, A Bionano Genomics Company  based inEl Segundo, CALIFORNIA (USA)
High-quality detection of CNV from NGS data has been a challenge for many years. BioDiscovery has perfected algorithms for the detection of CNV and AOH from almost all NGS ...
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:BioDiscovery, A Bionano Genomics Company  based inEl Segundo, CALIFORNIA (USA)
The most recent version of NxClinical, the leading copy number variation (CNV) analysis software for clinical cytogenetics and molecular labs, now includes an integrated ACMG guidelines scoreboard ...
by:BioDiscovery, A Bionano Genomics Company  based inEl Segundo, CALIFORNIA (USA)
The probe track view in NxClinical shows greater detail related to the supporting probes involved in this heteroUPD15 example. Enlarge the image to the right to reveal the heteroUPD15 visualized on both the top chromosome view (represented by the pink horizontal line) and the BAF plot for parental informative SNPs ...
by:BioDiscovery, A Bionano Genomics Company  based inEl Segundo, CALIFORNIA (USA)
Within the karyogram view, vertical bars are drawn within the AOH affected chromosome(s) to indicate parent-of-origin (pink=maternal; blue=paternal), and the same color indicators are displayed in the zygosity track. The image to the left displays a maternal inheritance represented by the pink probes on the BAF ...
by:BioDiscovery, A Bionano Genomics Company  based inEl Segundo, CALIFORNIA (USA)
In addition to using the scoreboard as a stand-alone guideline, this new feature can also be coupled with NxClinical's popular automated variant pre-classification decision tree to pre-classify events. This allows analysts to quickly sort through the events on the table and prioritize for ...
by:BioDiscovery, A Bionano Genomics Company  based inEl Segundo, CALIFORNIA (USA)
When analyzing SNP data, NxClinical users who deploy this new feature can now further investigate uniparental heterodisomy events within duos and trios with one simple click - saving them valuable time during the review process. ...
by:BioDiscovery, A Bionano Genomics Company  based inEl Segundo, CALIFORNIA (USA)
BioDiscovery has developed two algorithms for the detection of CNV and AOH events from NGS using its decades-long expertise in the area. One algorithm, the “Self-reference” algorithm, can be used for all WGS data regardless of sequencing depth. The second is the “Multi-Scale Reference” (MSR) algorithm that is applicable to all NGS data (WGS, WES, and Gene panels). The MSR ...
by:BioDiscovery, A Bionano Genomics Company  based inEl Segundo, CALIFORNIA (USA)
Getting CNV calls from Whole Exome Sequencing has been one of the most challenging efforts in the community. There have been numerous algorithms proposed but they suffer either from poor sensitivity or too many false-positive calls. The MSR algorithm has been able to offer the best balance of these competing measures, detecting small true-positives without generating many false-positives. The ...
by:BioDiscovery, A Bionano Genomics Company  based inEl Segundo, CALIFORNIA (USA)
The MSR algorithm can be applied to any gene panel from single gene (e.g. DMD test) to large panels having thousands of gene. The image below is from the Illumina TruSightTM Oncology 500 (TSO500) panel showing a somatic cancer profile. The cytogenetic complexity of the tumor sample is clearly evident with a large copy number gain of 8p and loss of a large section of 13q. Aberrations associated ...
by:BioDiscovery, A Bionano Genomics Company  based inEl Segundo, CALIFORNIA (USA)
The MSR algorithm can also be applied to detect CNVs from shallow sequencing, including very low-level mosaic events seen in NIPS or ctDNA samples. The image below shows a sample with trisomy 21 detected using 1x WGS. CNVs are an important contributor to disease and are required for accurate diagnosis. For clinical sequencing to be fully accepted as a replacement for microarrays and other ...
by:Cognuse  based inSan Diego, CALIFORNIA (USA)
CoNurse is a voice-guided protocol adherence and deployment application. Our platform provides step-by-step instructions for clinical procedures at the point of care, enforcing adherence to protocols and improving the quality and standardisation of care across the care ...
by:Cortechs.ai  based inSan Diego, CALIFORNIA (USA)
NeuroQuant® CT is an FDA-cleared quantitative imaging solution that provides consistent views of head CT exams and automated quantitative measurements to improve workflow efficiency, measurement accuracy, and clinical confidence. The software corrects for sub-optimal patient positioning, improves conspicuity over time, and improves the measurement of change over ...
by:Cortechs.ai  based inSan Diego, CALIFORNIA (USA)
For the assessment of traumatic brain injury and other neurodegenerative conditions. The NeuroQuant TBA Report provides physicians a quick reference and in-depth look on regional and global brain structure volumes, which could occur as a result of a brain injury or neurodegenerative disease, by providing volume measurements of 47 brain structures for both the right and left hemisphere, total ...
by:Cortechs.ai  based inSan Diego, CALIFORNIA (USA)
OnQ Neuro is FDA-cleared post-processing software used by radiologists, oncologists, and other clinicians to assist with the analysis and quantification of MR images of brain ...