ManageEngine Log360
Log360 is a SIEM or security analytics solution that helps you combat threats on premises, in the cloud, or in a hybrid environment. It also helps organizations adhere to compliance mandates such as PCI DSS, HIPAA, GDPR and more. You can customize the solution to cater to your unique use cases and protect your sensitive data.
With Log360, you can monitor and audit activities that occur in your Active Directory, network devices, employee workstations, file servers, databases, Microsoft 365 environment, cloud services and more. Log360 correlates log data from different devices to detect complex attack patterns and advanced persistent threats. The solution also comes with a machine learning based behavioral analytics that detects user and entity behavior anomalies, and couples them with a risk score. The security analytics are presented in the form of more than 1000 pre-defined, actionable reports. Log forensics can be performed to get to the root cause of a security challenge.
The built-in incident management system allows you to automate the remediation response with intelligent workflows and integrations with popular ticketing tools.
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Parallels RAS
Parallels® RAS meets you where you are in your virtualization journey—bridging on-premises and multi-cloud solutions into a centralized management console for administrators and a secure virtual work environment for end users.
Enjoy an all-in-one digital workspace and remote work solution that provides secure virtual access to business applications and desktops on any device or OS—from anywhere. Agile, cloud-ready foundation and end-to-end security fueled by a centralized management console with granular policies is at your fingertips. Take advantage of on-premises, hybrid, or public cloud deployments and integrate with existing technology like Microsoft Azure and AWS. Gain the flexibility, scalability, and IT agility you need to quickly adapt to changing business needs. Best of all, Parallels RAS offers a single, full-featured licensing model that includes 24/7 support and access to free training.
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Evo 2
Evo 2 represents a cutting-edge genomic foundation model that excels in making predictions and designing tasks related to DNA, RNA, and proteins. It employs an advanced deep learning architecture that allows for the modeling of biological sequences with single-nucleotide accuracy, achieving impressive scaling of both compute and memory resources as the context length increases. With a robust training of 40 billion parameters and a context length of 1 megabase, Evo 2 has analyzed over 9 trillion nucleotides sourced from a variety of eukaryotic and prokaryotic genomes. This extensive dataset facilitates Evo 2's ability to conduct zero-shot function predictions across various biological types, including DNA, RNA, and proteins, while also being capable of generating innovative sequences that maintain a plausible genomic structure. The model's versatility has been showcased through its effectiveness in designing operational CRISPR systems and in the identification of mutations that could lead to diseases in human genes. Furthermore, Evo 2 is available to the public on Arc's GitHub repository, and it is also incorporated into the NVIDIA BioNeMo framework, enhancing its accessibility for researchers and developers alike. Its integration into existing platforms signifies a major step forward for genomic modeling and analysis.
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Genome Analysis Toolkit (GATK)
Created within the Data Sciences Platform at the Broad Institute, this comprehensive toolkit provides an extensive array of features primarily aimed at variant discovery and genotyping. With its robust processing engine and high-performance computing capabilities, it is equipped to manage projects of any magnitude. The GATK has established itself as the industry benchmark for detecting SNPs and indels in both germline DNA and RNA sequencing data. Its functionalities are now broadening to encompass somatic short variant detection as well as addressing copy number variations (CNV) and structural variations (SV). Besides the core variant callers, the GATK incorporates numerous utilities for executing associated tasks, including the processing and quality assurance of high-throughput sequencing data, and it comes bundled with the well-known Picard toolkit. Originally designed for exome and whole genome data generated via Illumina sequencing technology, these tools are versatile enough to be modified for use with various other technologies and study designs. As research evolves, the adaptability of the GATK ensures it remains relevant in diverse genomic investigations.
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