6 projects tagged "LGPL 2.1"
ivykis is a library for asynchronous I/O readiness notification. It is a thin, portable wrapper around OS-provided mechanisms such as /dev/poll, epoll_create(2), kqueue(2), poll(2), and port_create(3C). ivykis was mainly designed for building high-performance network servers, but can be used as building block for any kind of event-driven application that uses poll(2)able file descriptors as its inputs.
XWiki is a WikiWiki clone written in Java that supports many popular features of other Wikis like the Wiki syntax, version control, attachments, security, and searching, but also many advanced features like templates, database and dynamic development using scripting languages (Velocity, Groovy, Ruby, Python, PHP, and more), an extension system and skinability, J2EE scalability, an XML/RPC remote API, statistics, RSS feeds, PDF exporting, WYSIWYG editing, an Office viewer and importer, and a lot more.
ext-Dns is a core library, an extensible forward DNS server, and some additional tools designed to create DNS server solutions which are able to do any additional operation at the resolution level (running commands, rewritting replies, gathering stats, and so on), without any limit. It provides a ready-to-use solution in case you want to build a DNS server which takes additional actions at the resolution level in an easy way. That is, its design is focused on allowing people to implement whatever they like when a request is received, freeing them from most of the details which involves handling DNS protocol.
PhenoTips is a tool for collecting and analyzing phenotypic information for patients with genetic disorders. It combines an easy-to-use interface, compatible with any device which runs a Web browser, with a standardized database backend. The PhenoTips user interface closely mirrors clinician workflows, to facilitate the recording of observations made during the patient encounter. By collecting, classifying, and analyzing phenotypic information during the patient encounter, PhenoTips allows streamlining of clinic workflow, efficient data entry, improved diagnosis, standardization of collected patient phenotypes, and sharing of anonymized patient phenotype data for the study of rare disorders.