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<link rel="stylesheet" type="text/css" | <link rel="stylesheet" type="text/css" | ||
href="https://2018.igem.org/Team:Bielefeld-CeBiTec/CSS?action=raw&ctype=text/css" /> | href="https://2018.igem.org/Team:Bielefeld-CeBiTec/CSS?action=raw&ctype=text/css" /> | ||
+ | <link rel="stylesheet" href="https://cdnjs.cloudflare.com/ajax/libs/font-awesome/4.7.0/css/font-awesome.min.css"> | ||
+ | |||
+ | <script> | ||
+ | |||
+ | window.onscroll = function() {scrollFunction(); checkOffset();}; | ||
+ | |||
+ | function scrollFunction() { | ||
+ | if (document.body.scrollTop > 20 || document.documentElement.scrollTop > 20) { | ||
+ | document.getElementById("page-arrow-top").style.display = "block"; | ||
+ | } else { | ||
+ | document.getElementById("page-arrow-top").style.display = "none"; | ||
+ | } | ||
+ | } | ||
+ | |||
+ | function checkOffset() { | ||
+ | if($('#page-arrow-top').offset().top + $('#page-arrow-top').height() | ||
+ | >= $('#footer').offset().top - 10) | ||
+ | $('#page-arrow-top').css('position', 'absolute'); | ||
+ | if($(document).scrollTop() + window.innerHeight < $('#footer').offset().top) | ||
+ | $('#page-arrow-top').css('position', 'fixed'); // restore when you scroll up | ||
+ | } | ||
+ | |||
+ | function topFunction() { | ||
+ | document.body.scrollTop = 0; // For Chrome, Safari and Opera | ||
+ | document.documentElement.scrollTop = 0; // For IE and Firefox | ||
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</head> | </head> | ||
− | <div class=" | + | <body> |
− | < | + | |
− | + | <div class="title_picture"> | |
− | < | + | <img src="https://static.igem.org/mediawiki/2017/6/6c/T--Bielefeld-CeBiTec--title-img-bielefeld.jpg" style="width:100%"> |
+ | </div> | ||
+ | |||
+ | <div class="container"> | ||
+ | <div class="main_content"> | ||
+ | |||
+ | <div class="title">Software siRCon</div> | ||
+ | |||
+ | <article> | ||
+ | In our Project we introduce RNA interference (RNAi) and silencing with siRNAs as an alternative for CRISPR/Cas. To make use of our silencing vector system Tace, functional siRNA for prokaryotic organisms must be determined. Thus, we developed a siRNA construction tool, which can find possible siRNAs for a given gene sequence and calculate their gene silencing probability. It consists of the three modules RNAi, siRNA and check siRNA. Obtained siRNAs are perfectly compatible with our siRNA vector system. To the best of our knowledge, this is the first tool dedicated to predicting customized siRNA for the application in prokaryotes. This Python tool comes in two versions: a command line application and an easy-to-use graphical interface. | ||
+ | </article> | ||
+ | |||
+ | |||
+ | |||
</div> | </div> | ||
+ | |||
+ | <!-- Footer --> | ||
+ | <footer id="footer" class="w3-container w3-padding-32 w3-center w3-black w3-xlarge" style="position: absolute; width:100%; z-index:200;"> | ||
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+ | |||
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+ | |||
+ | </div> | ||
+ | |||
+ | </body> | ||
</html> | </html> |
Revision as of 21:36, 12 October 2018
Software siRCon