Search Results for "bis-snp"

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...

The Collaborative Computational Project for NMR (CCPN) provides tools and knowledge to maximise the impact of the biological NMR studies. The CCPN software facilitates data analysis and software integration. The project actively promotes the exchange of knowledge and provides training and best practices for the NMR community. CCPN also has a leading role in the development of a NMR data-sharing standard and coordination of NMR instrumentation proposals for RCUK and BIS. The 28 partners of CCPN...

Mini-Buchhaltung mit LibreOffice oder OpenOffice.org. Version 1.10.3 vom 9. Januar 2017 ACHTUNG: Aufgrund eines Bugs in LibreOffice Version 4.1.2 läuft das Programm nicht in dieser Version. Bis Version 4.0.1.2 funktioniert es und dann wieder an 4.1.3. Angebotserstellung, Rechnungserstellung, Lager und Kundenverwaltung, sowie Buchhaltung mit Einnahmen-Überschuß-Rechnung in einer einzigen ODS-Datei. Angebote können in Rechnungen übernommen werden. Es sind 2 Steuersätze (und 0%) in einer...

SPRITE is an open-source software package providing a parallel implementation of the Single Nucleotide Polymorphisms (SNP) detection genomic data analysis workflow. It consists of three tools: PRUNE for read alignment, SAMPA for intermediate file processing, and PARSNIP for parallel SNP calling.

GOBIG is a toolbox that can be used for detecting genetic variations. The project is intended to handle big data. What's more important is that it be used to detect clusters of SNP variants. It is the intention to use the toolbox with common and rare variants. To use it, for example, to find the genetic map of genes causing complex diseases.

In consanguineous families, as a result of inheriting the same genomic segments through both parents, the individuals have stretches of their genomes that are homozygous. This situation leads to the prevalence of recessive diseases among the members of these families. Homozygosity mapping is based on this observation and several recessive disease genes have been discovered with the help of this technique in consanguineous families. The researchers typically use SNP arrays to determine...

DNAA is the DNA analysis package, for analyzing next-generation post-alignment whole genome resequencing data. Specifically, DNAA is able to find structural variation, SNP and indel variants, as well as evaluating the mapping and data quality.

A program for visualising Affymetrix SNP array data for identification regions of homozygosity. Written to aid autozygosity mapping and aid the discovery of potential disease loci.

mendelFix is a Perl script for checking Mendelian errors in genome-wide SNP data of trio designs. The program takes 12-recoded PLINK PED and MAP files as input, and calculates a series of summary statistics for Mendelian errors, sets as missing offspring genotypes that present Mendelian inconsistencies, and implements a simplistic procedure to infer missing genotypes using parent information. The program can be easily incorporated in any pipeline for family-based SNP data analysis...

We developed DMET-Analyzer a tool for the automatic association analysis among the variation of the patient genomes and the clinical conditions of patients, i.e. the different response to drugs. The proposed system allows: (i) to automatize the workflow of analysis of DMET-SNP data avoiding the use of multiple tools; (ii) the automatic annotation of DMET-SNP data and the search in existing databases of SNPs (e.g. dbSNP), (iii) the association of SNP with pathway through the search...

SNP-Analyzer is a tool for the efficient Analysis and management of Affymetrix SNP DMET Data analysis

BotenInschrijfSysteem (Boat Registration System) is a tool with which members of a rowing club can see which boats are available and make reservations. Now your club no longer needs a paper reservation book, saving your members a lot of time! Important note: the SourceForge repository will not be updated anymore as of 1st March, 2012. Instead, we've moved to GitHub: https://github.com/erikroos/BIS

Avenzoar is a one-year exploration of renal cell carcinoma morphology and its related single nucleotide polymorphisms (SNPa) as a method of automating diagnosis of cancer by using a computer-aided decision tree controlled by analytical statistics.

GNU BIS is a project to create an open source corporate portal. Right now it includes a collaborative framework for contact (not only customer!) relationship management. The next releases will include project management, products and services.