var fDesc=new Array();
fDesc[0] = "It&#039;s a data analysis tool with detection of genome-wide copy number changes.<br /> <br /> Main Features:<br /> <br /> -From alignment of raw data to categorization and annotation of mutations in three simple steps<br /> -Supports four different types of analysis: Single Sample, Tumor-Normal, Trio and OneSeq CNV and Mutation Analysis<br /> -Supports variant annotation from many public sources, including NCBI, COSMIC, PubMed, ClinVar and custom annotation<br /> -Reduces time-to-results from days to hours without complex IT infrastructure or special hardware";

function tShowHide(id, show)
{
	var s = document.getElementById("desc");

	if ((s.innerHTML.length<=212 || show==1) && show!=2)
	{
		s.innerHTML = fDesc[id];
		if (document.getElementById('m1'))
			document.getElementById('m1').style.display='none';
		if (document.getElementById('m2'))
			document.getElementById('m2').style.display='none';
		if (document.getElementById('more_txt'))
			document.getElementById('more_txt').style.display='inline';
	}
	else
	{
		s.innerHTML = '';
	}
}