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Showing 27 open source projects for "sv"
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Red Hat Enterprise Linux (RHEL) on Microsoft Azure provides a secure, reliable, and flexible foundation for your cloud infrastructure. Red Hat Enterprise Linux on Microsoft Azure is ideal for enterprises seeking to enhance their cloud environment with seamless integration, consistent performance, and comprehensive support.
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Our robust pre-built connectors and our no-code, drag-and-drop interface makes it easy and fast to automatically sync vendors, invoices, and invoice payment data between Tipalti and your ERP or accounting software.
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Dayon! (active)
Remote assistance made easy!
Dayon! is an open source remote desktop and assistance solution. It is easy to use, secure, requires no registration and is free for personal and commercial use! -
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Sparx' EA - MDG for TRAK
MDG for Sparx' Enterprise Architect to Create TRAK arch. descriptions
Custom add-in (MDG technology) for Sparx Systems Enterprise Architect UML modelling tool (https://sparxsystems.com/products/ea/index.html) to create architecture descriptions using TRAK https://sf.net/projects/trak Provides: - the set of TRAK views that can be represented using UML and SysML . Each view display a custom toolbox palette with the objects and relationships that are needed for that TRAK view - relationships can be made directly from the objects on a view using the... -
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... in the higher leve 5. removehierarchy : Verilog Hierarchy Removal Tool to ungroup all the instances in a given module 6. comparemoduleinterfaces - Diff module ports and parameter. Tool to compare the interfaces ( ports, parameters, SV interfaces ) between two versions of a Verilog module or two similar modules 7. Verilog Testbench Generator 8. VHDL Testbench Generator 9. Verilog Remove Assignments 10. Verilog Find Instances or Nets 11. Clock And Reset Tree Analyzer( Alpha)
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PhaseDel
Phasing-based somatic deletion caller from single-cell WGS data
PhaseDel is a Java-based variant caller designed for detecting somatic deletions from single-cell whole-genome sequencing (scWGS) data. It is highly specialized for discriminating genuine somatic focal deletions (several bases to kilo-bases in length) from excessive SV-like artifacts, which are inevitably occurring during single-cell whole-genome amplification. PhaseDel accurately detects such true deletions based on the linkage information between deletion breakpoints and nearby germline... -
BrightGauge, a ConnectWise solution, was started in 2011 to fill a missing need in the small-to-medium IT Services industry: a better way to manage data and provide the value of work to clients. BrightGauge Software allows you to display all of your important business metrics in one place through the use of gauges, dashboards, and client reports. Used by more than 1,800 companies worldwide, BrightGauge integrates with popular business solutions on the market, like ConnectWise, Continuum, Webroot, QuickBooks, Datto, IT Glue, Zendesk, Harvest, Smileback, and so many more. Dig deeper into your data by adding, subtracting, multiplying, and dividing one metric against another. BrightGauge automatically computes these formulas for you. Want to show your prospects how quick you are to respond to tickets? Show off your data with embeddable gauges on public sites.
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vulscan
Advanced vulnerability scanning with Nmap NSE
Vulscan is a module that enhances nmap to a vulnerability scanner. The nmap option -sV enables version detection per service which is used to determine potential flaws according to the identified product. The data is looked up in an offline version of VulDB. -
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svdetect.sh is a shell script to run SVDetect to detect SV in exome-seq and Shatterproof to detect chromothripsis. ***Update*** The output files of SVDetect can be annotated by genes with multi-threading.
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inGAP-family provides an efficient and effective framework to discover, filter and visualize DNA polymorphisms and structural variants from alignment of short reads. Applying this method on polymorphism detection on real datasets shows that elimination of artificial variants greatly facilitates the precise identification of meiotic recombination points, recognizing causal mutations in mutant genomes or QTL loci. In addition, inGAP-family provides user-friendly graphical interface for...
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ConnectWise ScreenConnect, formerly ConnectWise Control, is a remote support solution for Managed Service Providers (MSP), Value Added Resellers (VAR), internal IT teams, and managed security providers. Fast, reliable, secure, and simple to use, ConnectWise ScreenConnect helps businesses solve their customers' issues faster from any location. The platform features remote support, remote access, remote meeting, customization, and integrations with leading business tools.
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meerkat.sh
script of SV calling in Exome-seq
meerkat.sh is a shell script to run Meerkat for SV detection in Exome-seq. The script accepts single BAM or paired tumor-normal BAMs. -
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novoBreak
Robust detection of somatic structural breakpoints in cancer genomes
novoBreak is a tool used in cancer genomic studies to discover SV (both somatic and germline) breakpoints. It can report accurate breakpoints of Deletions (DEL), Duplications (DUP), Inversions (INV) and Translocations (TRA) (you should consider some of them are mobile elements insertions or templated insertions). For novel insertions, we may only report the breakpoints but not the inserted sequence. Please forget about novel insertions at the moment. We will work on that later... -
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Swedish-English Open Dictionary
Swe-Eng Kindle Dictionary Based on Folkets Lexikon
This is a transcoded and reformatted version of "The People's Dictionary" (Folkets Lexikon, see http://folkets-lexikon.csc.kth.se for more information). The project contains encoding and formatting scripts along with instructions for converting the dictionary database into a Kindle book. The dictionary is in the Kindle's native dictionary format and integrates with the Smart Lookup feature which allows you to access words definitions without leaving your book page - just press and hold to... -
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LAMSA
Long Approximate Matches-based Split Aligner
LAMSA (Long Approximate Matches-based Split Aligner) is a novel split alignment approach with faster speed and good ability of handling SV events. It is well-suited to align long reads (over thousands of base-pairs). -
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SCNVSim
SCNVSim, a tool to simulate somatic CNV and Strucuture Variants
SCNVSim is a Bioinformaitcs tool developed in Java programming language for the simulation of somatic copy number variations and structure variations in cancer genome studies. The tool is capable of simulating features related to tumor samples including tumor purity, aneuploidy and heterogeneity other than common types of SV and CNV. SCNVSim generates the genomes of a cancer cell population with detailed information of copy number status, loss of heterogeneity, and structure variation break... -
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SVMerge is a meta structural variation (SV) calling pipeline, which makes SV predictions with a collection of SV callers which are then, merged, and computationally validated using local de novo assembly.
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MERAP
Medical Resequencing Analysis Pipeline
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SV Media Player Full HD
new media player Portable Open Source
Ultimate Full HD Portable Media player with Ckfs Technology which we introduced for HD files Download and Enjoy Movies -
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Structural Variant Detection
SV detection in paired end whole genome sequencing data
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isvm: incremental svm implementation for Stephe ruiping's algorithm based on libsvm svmovoovr: implement for OVO OVR classification. pso-svm: PSO svm implementation
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The SV CMS is an CMS with an userfriendly interface. There is an tool for users, a page tool and much more.
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