Search Results for "bis-snp"
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Showing 186 open source projects for "bis-snp"
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HubSpot is an AI-powered customer platform with all the software, integrations, and resources you need to connect your marketing, sales, and customer service. HubSpot's connected platform enables you to grow your business faster by focusing on what matters most: your customers.
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HubSpot is an AI-powered customer platform with all the software, integrations, and resources you need to connect your marketing, sales, and customer service. HubSpot's connected platform enables you to grow your business faster by focusing on what matters most: your customers.
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JKSV
JK's Save Manager Switch Edition
This started as a simple, straight port of my 3DS save manager I publicly released in 2016. Despite not originally wanting to take it too far, I continued working on it for fun when I can. Dump and restore account save data. Dump and restore device saves shared by all users (Games such as Animal Crossing). Dump and restore BCAT Data. Dump and restore cache Saves. Dump system save data. Dumping this data is always enabled, but writing back needs to be enabled from the options menu. Writing to... -
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BQSKit
Berkeley Quantum Synthesis Toolkit
The Berkeley Quantum Synthesis Toolkit (BQSKit) [bis • kit] is a powerful and portable quantum compiler framework. It can be used with ease to compile quantum programs to efficient physical circuits for any QPU. A standard workflow utilizing BQSKit consists of loading a program into the framework, modeling the target QPU, compiling the program, and exporting the resulting circuit. -
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kSNP
kSNP4 does SNP discovery and SNP annotation from whole genomes
kSNP4 identifies the pan-genome SNPs in a set of genome sequences, and estimates phylogenetic trees based upon those SNPs. SNP discovery is based on k-mer analysis, and requires no multiple sequence alignment or the selection of a reference genome, so kSNP4 can take 100's of microbial genomes as input. A SNP locus is defined by an oligo of length k surrounding a central SNP allele. kSNP4 can analyze both complete (finished) genomes and unfinished genomes in assembled contigs or raw... -
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VitalSignsCapture
Download data from medical device interfaces in ICU & Anaesthesia
A C# .NET app to download or capture data from several medical device interfaces such as Datex AS3 S/5 Anesthesia, Philips Intellivue, GE Dash, Mindray, Spacelabs, Draeger Infinity, Draeger HL7 patient monitors, GE Engstrom, Draeger (Medibus), Maquet (Servo-i & Flow-i), Puritan Bennett ventilators, Covidien BIS Vista cerebral monitor, Fresenius Agilia, Alaris Carefusion, BBraun Spacecom syringe and volumetric pumps, Roche Cobas ASTM ABG analyzers. Requires Visual Studio 2022, .NET 8 or Visual... -
With Twilio Voice, you can build unique phone call experiences with one API, to create, receive, control and monitor calls with just a few lines of code. Create an engaging voice experience that you can quickly scale and modify with a wide array of customization options and resources.
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A tool to estimate trends in recent effective population size trajectories using genome-wide SNP data.
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AundS
Programm zur Eingabe für Arbeits- und Sozialnoten
Bis zu 10 Lehrer können Sozialnoten für ihre Schüler eingeben. Es wird ein Durchschnitt angezeigt und man kann die Durchschnittsnoten der SuS in einer Datei speichern -
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NIC Kommander
Ersatz für den Norton Commander
NIC imitiert einen Norton Commander für Windows 95 bis Windows 10 und weitere Versionen. Der Editor Hexkon eingnet sich sowohl Textdateien wie auch für Binärdateien. -
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somatic.sh
script for somatic SNP and Indel calling
somatic.sh is a shell script to run varscan somatic for somatic variant-calling, and Annovar to annotate. It calls both SNPs and Indels. It also produces 2 MAF files compatible with MutSigCV. Now the script allows for multithreading. The script is updated according to new format. -
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PaintBrutsch
Ein Malprogramm, das selbst Microsoft gefallen dürfte
Ein Malprogramm, ähnlich dem Paint von Windows 95 bis Windows XP, das sogar noch unter den neuesten Windowsverionen läuft mit einigen erweiterten Funktionen, wie Kontrast und Farbreduktion, zum Editieren von einfachen Ikonen und Kursoren geeignet, kein Fotoshop! -
Every customer interaction is vital to your business success and revenue growth. With Jiminny’s AI-powered conversation intelligence software, we take recording, capturing, and meticulous analysis of call recordings to the next level. Unlock call analytics that provide actionable insights with our call tracking software, empowering you to identify what's working and what's not. Seamlessly support your biggest objectives across the entire business landscape with our innovative call tracking system.
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ntx
Neutrality tests using the SNP site frequency spectrum
Tests on "neutrality" are designed to detect systematic deviations from chance patterns in genetic data. This tool computes for a given SNP site frequency spectrum some standard test statistics like Tajima's D, Fay & Wu's H, etc. Additionally, the user may adapt the tests to specific demographies by specifying non-standard first and secondary moments. These can be obtained e.g. from simulations. -
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DSXR18
Aautomatically downloads snapshots from the Behringer XR18
... name. *.scn files are compatible with the X-AIR-Edit program. https://www.buymeacoffee.com/piotrzaczek/dsxr18-kopiuje-snp-z-xr18 -
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PhaseDel
Phasing-based somatic deletion caller from single-cell WGS data
... heterozygous SNP sites. The important features of PhaseDel are: • Accurate identification of somatic focal deletions at single-base-pair resolution in scWGS using phasing information • Estimation of the genome-wide somatic deletion rate for a given cell with the controlled FDR level • Characterization of underlying DSB repair mechanisms for identified deletion candidates A more detailed description of the tool is provided in the [[wiki]] tab. -
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EXCEL-ArbeitsZeitErfassung
Work time tracking EXCEL file in German
This project was mainly made for German-speaking users and countries (Germany, Austria, Switzerland), therefore this description/summary is written in German. Diese EXCEL-Datei dient der Arbeitszeiterfassung. Sie berechnet automatisch die Arbeitszeit anhand der Voreinstellungen und der eigenen Eingaben. Die ausdruckbaren Blätter eignen sich unterschrieben als Arbeitszeitnachweis. Folgende Tabellenblätter sind enthalten: - Copyright - Einstellungen - Januar bis Dezember (12 Blätter... -
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gsasnp2
PubMed ID: 29562348 / DOI: 10.1093/nar/gky175
* GSA-SNP2 is a successor of GSA-SNP (Nam et al. 2010, NAR web server issue). GSA-SNP2 accepts human GWAS summary data (rs numbers, p-values) or gene-wise p-values and outputs pathway genesets ‘enriched’ with genes associated with the given phenotype. It also provides both local and global protein interaction networks in the associated pathways. * Article: SYoon, HCTNguyen, YJYoo, JKim, BBaik, SKim, JKim, SKim, DNam, "Efficient pathway enrichment and network analysis of GWAS summary data using... -
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snpEff is a fast variant effect predictor (SNP, MNP and InDels) for genomic data. It is integrated with Galaxy so it can be used either as a command line or as a web application.
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MetaPhat -meta-pheno-association-tracker
Multivariate traits genome-wide association analysis and decomposition
MetaPhat is an open sourced program to detect optimal subset traits on lead SNP associations from multiple biomarker GWAS summary results. Best traits are derived from systematic decomposing multivariate associations into central traits based on optimal BIC and P-value from multivariate CCA models. SNP trace results are plotted and clustered to dissect and improve the specificity of mv phenotype-genotype associations. released with LD function https://sourceforge.net/projects/meta-pheno... -
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RNASeqBrowser
RNASeqBrowser: A genome browser for strand specific RNAseq reads
Strand specific RNAseq data is now more common in RNAseq projects. The most widely used visualization tool is the UCSC genome browser that introduced the custom track concept that enabled researchers to simultaneously visualize gene expression at a particular locus from multiple experiments. This paper introduces a visualization tool (RNASeqBrowser) that incorporates and extends the functionality of the UCSC genome browser. For example, RNASeqBrowser simultaneously displays read coverage,... -
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ParseCNV CNV call association software takes CNV calls as input and creates SNP based statistics for CNV occurrence in population study cases and controls then calls CNVRs based on neighboring SNPs of similar significance.
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Protokoll
Ein standalone Protokollprogramm
Ein eigenständiges Programm zur Erzeugung von Betriebsratsprotokollen. Teile davon sind Bestandteil des Projektes „Sysiphus BER“, die Entwicklung dieses Programmes hat jedoch schlicht das Hauptprojekt überholt. Das Programm basiert auf „Tagesordnungspunkten“, wobei so ein Punkt alles von einer Überschrift, ein einfacher Text bis hin zu einer Einstellung mit Beschluss sein kann. Dazu kann man solche TOP’s spezialisieren und Metadaten (z.B. MA-Name, MA-Vorname, etc.) hinzufügen. Es kann ein... -
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MIRA - Sequence assembler and sequence mapping for whole genome shotgun and EST / RNASeq sequencing data. Can use Sanger, 454, Illumina and IonTorrent data. PacBio: CCS and error corrected data usable, uncorrected not yet.
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hppRNA
A Snakemake-based handy parameter-free pipeline for RNA-Seq analysis
hppRNA package is dedicated to the RNA-Seq analysis for a large number of samples simultaneously from the very beginning to the very end, which is formulated in Snakemake pipeline management system. It starts from fastq files and will produce gene/isoform expression matrix, differentially-expressed-genes, sample clusters as well as detection of SNP and fusion genes by combination of the state-of-the-art software. The first version handles protein-coding genes, lncRNAs and circRNAs and includes... -
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variantkey
Binary files for variantkey
Binary files for the variantkey library: https://github.com/Genomicsplc/variantkey The binary files are generated using the script: https://github.com/Genomicsplc/variantkey/blob/master/resources/tools/vkhexbin.sh from the Human Variation Sets in VCF Format [National Library of Medicine (NLM)]: ftp://ftp.ncbi.nih.gov/snp/organisms/ -
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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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Primzahlen-Suchen_3
Searching primes with brute force, Parallel.For up to 20 digits
- Brute Force Methode bis 20 Stellen - C# Console - Parallel.For Methode - very fast Topics: prime