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	<title>Bioinformatics and BioStatistics Method Forum</title>
	<description></description>
	<link>http://www.protocol-online.org/forums/index.php</link>
	<pubDate>Fri, 20 Nov 2009 16:23:06 -0800</pubDate>
	<ttl>360</ttl>
	<item>
		<title>Finding the ITS region in my sequence</title>
		<link>http://www.protocol-online.org/forums/index.php?showtopic=11684</link>
		<description><![CDATA[I need to see if I can find the ITS region in my sequences.  I have sequences from amplified 18s region and it is possible that I picked up the ITS region.  How do I approach this problem?  I don't know what to look for in my sequences.  I am new to bioinformatics, and any help is appreciated.]]></description>
		<pubDate>Thu, 19 Nov 2009 16:12:49 -0800</pubDate>
		<guid>http://www.protocol-online.org/forums/index.php?showtopic=11684</guid>
	</item>
	<item>
		<title>programm to view blastn 2.2.18 xml output file</title>
		<link>http://www.protocol-online.org/forums/index.php?showtopic=11651</link>
		<description><![CDATA[Dear people,<br />    <br />      i've got a blastn xml-output file from a bioinformatic and i'm now looking for a programm able to visualize this xml-output file. I've tried blast2go, but it gives me no information on the sequence and i want to see the different sequences aligned to each other, like in the web blast output. What's the programm of choice for such a task? I've no clue?<br /><br />Many thanks in advance for your help!<br /><br />Regards,<br />               p]]></description>
		<pubDate>Wed, 18 Nov 2009 12:34:51 -0800</pubDate>
		<guid>http://www.protocol-online.org/forums/index.php?showtopic=11651</guid>
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	<item>
		<title>Sequencher</title>
		<link>http://www.protocol-online.org/forums/index.php?showtopic=11639</link>
		<description><![CDATA[Hello everybody!<br /><br />I have got a problem. I did PCR and sequencing of nuclear Internal Transcribed Spacer (ITS) of a plant using two primers ITS1(forward) and ITS4 (reverse) . The PCR was quite successful. I employed the same primers for  sequencing reaction and got two clean sequences (forward and reverse) without secondary peaks. I used the SEQUENCHER software to make the consensus sequence, however, the forward and reverse sequences appear in the same direction. Why the sequences obtained from forward and reverse primers didn't run in opposite directions in sequencher?  PLEASE HELP. Thank you in advance!!!!!! <br /><br />Sincerely,<br />]]></description>
		<pubDate>Wed, 18 Nov 2009 04:18:51 -0800</pubDate>
		<guid>http://www.protocol-online.org/forums/index.php?showtopic=11639</guid>
	</item>
	<item>
		<title>redundant and non redundant</title>
		<link>http://www.protocol-online.org/forums/index.php?showtopic=11631</link>
		<description><![CDATA[can any  one please tell me ,whats the meaning of redundant and non redundant sequences ?<br /><br />thanx]]></description>
		<pubDate>Tue, 17 Nov 2009 21:00:41 -0800</pubDate>
		<guid>http://www.protocol-online.org/forums/index.php?showtopic=11631</guid>
	</item>
	<item>
		<title>How to search small sequences?</title>
		<link>http://www.protocol-online.org/forums/index.php?showtopic=11630</link>
		<description><![CDATA[Hi Everyone..!<br />I want to search whether a particular inverted repeat sequence present in the promoter region of E.coli gene is also present in other species of bacteria. Since it is just a 20bp long region, I dont know how to use NCBI blast option sad.gif guide me pls rolleyes.gif . I thank all of you..<br /><br /><br /><br /><br />Abhay]]></description>
		<pubDate>Tue, 17 Nov 2009 20:00:01 -0800</pubDate>
		<guid>http://www.protocol-online.org/forums/index.php?showtopic=11630</guid>
	</item>
	<item>
		<title>Search homologus sequences</title>
		<link>http://www.protocol-online.org/forums/index.php?showtopic=11628</link>
		<description><![CDATA[Hi Everyone..!<br />I want to search whether a particular inverted repeat sequence present in the promoter region of E.coli gene is also present in other species of bacteria. Since it is just a 20bp long region, I dont know how to use NCBI blast option <img src="http://www.protocol-online.org/forums/style_emoticons/default/sad.gif" style="vertical-align:middle" emoid=":(" border="0" alt="sad.gif" />  guide me pls <img src="http://www.protocol-online.org/forums/style_emoticons/default/rolleyes.gif" style="vertical-align:middle" emoid=":rolleyes:" border="0" alt="rolleyes.gif" /> . I thank all of you..<br /><br /><br /><br /><br />Abhay]]></description>
		<pubDate>Tue, 17 Nov 2009 19:56:42 -0800</pubDate>
		<guid>http://www.protocol-online.org/forums/index.php?showtopic=11628</guid>
	</item>
	<item>
		<title>exon intron location</title>
		<link>http://www.protocol-online.org/forums/index.php?showtopic=11626</link>
		<description>how to find intron exon location in plant dna?</description>
		<pubDate>Tue, 17 Nov 2009 18:18:03 -0800</pubDate>
		<guid>http://www.protocol-online.org/forums/index.php?showtopic=11626</guid>
	</item>
	<item>
		<title>Storage of sequencing files</title>
		<link>http://www.protocol-online.org/forums/index.php?showtopic=11584</link>
		<description><![CDATA[Dear people,<br /><br />     does anyone know a software solution to the storage of sequencing files. I always have problems with handling them because you download them and put it in a directory but after a while hundreds of them are accumulating and if you are looking for a spcific one after a while its like searching a needle in the haystack! Is there a prog like for example itunes to handle sequencing files?<br /><br />Many thanks in advance!<br /><br />Regards,<br />               p]]></description>
		<pubDate>Mon, 16 Nov 2009 14:03:27 -0800</pubDate>
		<guid>http://www.protocol-online.org/forums/index.php?showtopic=11584</guid>
	</item>
	<item>
		<title>receptor interaction software</title>
		<link>http://www.protocol-online.org/forums/index.php?showtopic=11504</link>
		<description><![CDATA[hi<br /><br />i want to know ,is there any program or software available on net , which can tell u about interactions among receptor and its  corresponding legend. <br /><br />which can tell about  bond formation or interaction that happened during receptor and legand interaction.<br /><br />i will be thankfull .<br />]]></description>
		<pubDate>Thu, 12 Nov 2009 20:41:59 -0800</pubDate>
		<guid>http://www.protocol-online.org/forums/index.php?showtopic=11504</guid>
	</item>
	<item>
		<title>Xenopus genome</title>
		<link>http://www.protocol-online.org/forums/index.php?showtopic=11484</link>
		<description><![CDATA[Hey all,<br /><br />Yet another quick question! Can anyone tell me if the Xenopus genome is fully annotated yet?<br /><br />Kami]]></description>
		<pubDate>Thu, 12 Nov 2009 03:26:26 -0800</pubDate>
		<guid>http://www.protocol-online.org/forums/index.php?showtopic=11484</guid>
	</item>
	<item>
		<title>Two factor anova multiple comparison</title>
		<link>http://www.protocol-online.org/forums/index.php?showtopic=11435</link>
		<description><![CDATA[Hi,<br /><br />I know that for a model 1 ( fixed ) anova, it is meaningful to perform multiple comparisons ( like Tukey test ) and that for a model 2 ( random ) anova, it is not meaningful to perform multiple comparisons.<br /><br />I would like to know for a model 3 ( mixed ) anova if it is meaningful or not to perform multiple comparisons.<br /><br />Thank you very much  <img src="http://www.protocol-online.org/forums/style_emoticons/default/laugh.gif" style="vertical-align:middle" emoid=":lol:" border="0" alt="laugh.gif" />]]></description>
		<pubDate>Mon, 09 Nov 2009 20:10:25 -0800</pubDate>
		<guid>http://www.protocol-online.org/forums/index.php?showtopic=11435</guid>
	</item>
	<item>
		<title>Phylogenetic tree</title>
		<link>http://www.protocol-online.org/forums/index.php?showtopic=11372</link>
		<description>Does some body knows how to draw a phylogenetic tree of any family....</description>
		<pubDate>Thu, 05 Nov 2009 02:17:10 -0800</pubDate>
		<guid>http://www.protocol-online.org/forums/index.php?showtopic=11372</guid>
	</item>
	<item>
		<title>software for drawing a synteny map</title>
		<link>http://www.protocol-online.org/forums/index.php?showtopic=11363</link>
		<description><![CDATA[Dear all,<br />I just constructed a genetic map for cowpea and want to draw a synteny map with the published model legume genetic map.<br />many published documents contain some very beautiful syteny map but I don't know how to make such a map? by hand or there are already softwares to aid this?<br />Thanks very much for any of your answers!<br />Blessings!]]></description>
		<pubDate>Wed, 04 Nov 2009 22:39:41 -0800</pubDate>
		<guid>http://www.protocol-online.org/forums/index.php?showtopic=11363</guid>
	</item>
	<item>
		<title>What statistical test to perform again?</title>
		<link>http://www.protocol-online.org/forums/index.php?showtopic=11359</link>
		<description><![CDATA[Hi,<br /><br />Could someone guide me through this question plese?<br /><br /><a href="http://mathbin.net/36011" target="_blank">http://mathbin.net/36011</a><br /><br />what type of anova should I perform? It looks like a 3 factor anova, but i'm not sure if i'm on the right track.<br /><br />Any help would be appreciate, thanks  <img src="http://www.protocol-online.org/forums/style_emoticons/default/laugh.gif" style="vertical-align:middle" emoid=":lol:" border="0" alt="laugh.gif" />]]></description>
		<pubDate>Wed, 04 Nov 2009 16:12:13 -0800</pubDate>
		<guid>http://www.protocol-online.org/forums/index.php?showtopic=11359</guid>
	</item>
	<item>
		<title>E-values</title>
		<link>http://www.protocol-online.org/forums/index.php?showtopic=11346</link>
		<description><![CDATA[Hey all this is not my usual haunt but I have a question.... I have been aligning my protein sequence , trying to find a homologue in a different species.  The problem is its a bit fragmented and for a portion of it i have an e-value of e-139.  What does this mean?<br /><br />Thanks in advance,<br /><br />Kami]]></description>
		<pubDate>Wed, 04 Nov 2009 06:43:25 -0800</pubDate>
		<guid>http://www.protocol-online.org/forums/index.php?showtopic=11346</guid>
	</item>
	<item>
		<title>How to compare 20 samples?</title>
		<link>http://www.protocol-online.org/forums/index.php?showtopic=11339</link>
		<description><![CDATA[Hi all,<br />I have 20 samples and 4tests each. How can I present it in my paper? I tried the bar chart, but it seems that my samples are too many to be presented clearly.<br />I have found the attached chart but I donot know how to draw it.<br />any suggestion?<br />Many thanks in advance]]></description>
		<pubDate>Wed, 04 Nov 2009 03:19:56 -0800</pubDate>
		<guid>http://www.protocol-online.org/forums/index.php?showtopic=11339</guid>
	</item>
	<item>
		<title>What statistical test to perform?</title>
		<link>http://www.protocol-online.org/forums/index.php?showtopic=11325</link>
		<description><![CDATA[Hi,<br /><br />I'm having a hard time with all the different type of anova test and I'm stuck on a particular question, where I think, there is many possible answer.<br /><br /><a href="http://mathbin.net/35930" target="_blank">http://mathbin.net/35930</a><br /><br />so basically depending on if you think if there are others interaction, and that you can't test them, you could do :<br /><br />Model I two factor anova<br />Model II two factor anova<br />Model III two factor anova<br />or also<br />Nested anova<br />Split-plot test<br /><br />Personaly, if I understand well, I would go with a Model II two factor nested anova, does it make sense? Or there is just one possible test for this particular situation?<br /><br />Any help would be greatly appreciated, thank you <img src="http://www.protocol-online.org/forums/style_emoticons/default/laugh.gif" style="vertical-align:middle" emoid=":lol:" border="0" alt="laugh.gif" />]]></description>
		<pubDate>Tue, 03 Nov 2009 11:35:19 -0800</pubDate>
		<guid>http://www.protocol-online.org/forums/index.php?showtopic=11325</guid>
	</item>
	<item>
		<title>promoter analysis</title>
		<link>http://www.protocol-online.org/forums/index.php?showtopic=11312</link>
		<description>what is the best tools for promoter detection and analysis?</description>
		<pubDate>Mon, 02 Nov 2009 23:35:01 -0800</pubDate>
		<guid>http://www.protocol-online.org/forums/index.php?showtopic=11312</guid>
	</item>
	<item>
		<title>Anyone has qBase freeware?</title>
		<link>http://www.protocol-online.org/forums/index.php?showtopic=11311</link>
		<description><![CDATA[Hi there,<br /><br />Anyone has qBase freeware? Would appreciate it if I can get a hold on it for qPCR calculation. I tried downloading the qBasePlus at <a href="http://www.biogazelle.com/" target="_blank">http://www.biogazelle.com/</a> but the link seemed to take like forever to load.<br /><br />Would appreciate it if you can direct me to a new site to download (if the above site is no longer available)<br /><br />Thanks.]]></description>
		<pubDate>Mon, 02 Nov 2009 23:17:51 -0800</pubDate>
		<guid>http://www.protocol-online.org/forums/index.php?showtopic=11311</guid>
	</item>
	<item>
		<title>Ho wto find promoter locations in human genome</title>
		<link>http://www.protocol-online.org/forums/index.php?showtopic=11281</link>
		<description><![CDATA[Hi there,<br /><br /><br /> How to find the DNA sequence [-2000, +2000] relative to TSS and<br />   [+2001, end of gene] for<br />  1) L44140 COMT gene in human chromosome 22<br />  2) X52828  BCR gene in human chromosome 22<br />   <br /> Can some one help me...<br /><br />Thanks,<br />Arniker]]></description>
		<pubDate>Sun, 01 Nov 2009 03:02:31 -0800</pubDate>
		<guid>http://www.protocol-online.org/forums/index.php?showtopic=11281</guid>
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