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<title>Genomics</title>
<link>http://www.scientistsolutions.com/c204-genomics.html</link>
<description>Discussion on methodology for high-throughput genome scale analysis including next-generation sequencing, gene expression, SNP genotyping, CGH, bioinformatic approaches and useful software for genomic testing…
 Life Science Discussion</description>
<language>en-us</language> 
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<sy:updateBase>2005-05-05T12:00+00:00</sy:updateBase>
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<title>Simultaneous RNA and DNA extraction</title>
<link>http://www.scientistsolutions.com/t25156-simultaneous+rna+and+dna+extraction.html</link>
<description><![CDATA[Hi guys,<br />I want to isolate RNA and DNA from Anopheles mosquito samples. I have been trying different variations of the TRIzol protocol (back extraction buffer, sodium citrate) and have had little success in recovering good gDNA. My 260/230 ratios have generally been poor (0.30-0.60) and the absorbance peak at 270 nm! What's more puzzling is that when run on the gel, I get no bands!<br />I know there are some kits out there that can be a better alternative but I was wondering if any...]]></description>
<pubDate>Fri, 14 Dec 2012 05:05:00 GMT</pubDate>
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<title>Genomics careers in the U.S.</title>
<link>http://www.scientistsolutions.com/t24989-genomics+careers+in+the+u_s_.html</link>
<description><![CDATA[Please follow the link below to a current list of Genomics-related positions posted on HireLifeScience.com. Create a free professional profile to apply direct to hiring companies, upload your resume, post in our forums and begin building your network.<br />HireLifeScience.com is an employment resource and networking tool for the Pharmaceutical, Biotechnology, Medical Device and Life Science industries.  We work exclusively with direct employers only and no third party recruiters giving you dir...]]></description>
<pubDate>Wed, 05 Dec 2012 06:33:31 GMT</pubDate>
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<title>sequencing</title>
<link>http://www.scientistsolutions.com/t23500-sequencing.html</link>
<description><![CDATA[I have designed primers that bind to conserved regions,so that variable regions inbetween the conserved regions get amplified.<br />My main aim is to detect the microbial diversity in a given sample by amplifying the variable regions of different microbes.<br />I used to amplify variable regions and get a 340 bp product and with this product i used to clone it by topo vector and later on used to sequence each single clone by sanger sequencing and the sequences were very fine.<br />But when i gave the ...]]></description>
<pubDate>Fri, 13 Jul 2012 00:16:12 GMT</pubDate>
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<title>DNA extraction of adipose tissue</title>
<link>http://www.scientistsolutions.com/t21996-dna+extraction+of+adipose+tissue.html</link>
<description><![CDATA[  I have to obtein genomic DNA of adipose tissue. I can not do it with conventional protocol (that I use to liver DNA extraction). I think I need to do a previouse step...I use promega reagents (nuclei lysis, protein precipitation, rehydratation) and prot K, and Can anyone help me? <br />Thanks in advance!!!]]></description>
<pubDate>Tue, 14 Feb 2012 02:52:12 GMT</pubDate>
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<title>Need Help Finding loci for Genotyping Assay</title>
<link>http://www.scientistsolutions.com/t20785-need+help+finding+loci+for+genotyping+assay.html</link>
<description><![CDATA[I am hoping to develop a genotyping assay for a plant species in the Cannabacea family using the High Resolution Melt function on a Roche Lightcycler 480 qPCR unti. However, I am not sure how to go about finding a suitable hyper variable loci of our plants genome for the analysis, hoping someone might be able to help point me in the right direction or know a business or professional who could help in my search? I have read that the IGS and ITS of rDNA are good regions to look into.<br />]]></description>
<pubDate>Thu, 13 Oct 2011 00:59:34 GMT</pubDate>
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<title>NGS data analysis learning program</title>
<link>http://www.scientistsolutions.com/t20013-ngs+data+analysis+learning+program.html</link>
<description><![CDATA[ Hi Guys,<br />Bionivid is conducting NGS data analysis learning program at Bionivid's Genome-Informatics Learning Centre at Bangalore...For more details please visit the website or facebook profile<br />http://www.bionivid.com/learning.html<br />https://www.facebook.com/Bionivid<br />]]></description>
<pubDate>Wed, 17 Aug 2011 03:22:30 GMT</pubDate>
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<title>Genomics</title>
<link>http://www.scientistsolutions.com/t19155-genomics.html</link>
<description><![CDATA[ Compare and Contrast siRNA mediated knockdown and geneknock out, which among them is best for studying cross talk between  hormones???<br />Thanks <br />Annie]]></description>
<pubDate>Wed, 15 Jun 2011 02:57:42 GMT</pubDate>
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<title>Rapid sequencing enables analysis of German E. Coli ourbreak</title>
<link>http://www.scientistsolutions.com/t19005-rapid+sequencing+enables+analysis+of+german+e_+coli+ourbreak.html</link>
<description><![CDATA[Scientists at BGI have sequenced the genome of E. Coli behind the recent German outbreak. Their public release of this strain's sequence has enabled researchers all over the world to analyze and understand the reason for its virulence. See this link for the press release by BGI.<br />This article from Genomeweb is also very informative. A quote in this article from Alexander Mellmann, a scientist involved in this research, demonstrates the importance of rapid sequencing: &amp;quot;&amp;quot;Speed is v...]]></description>
<pubDate>Mon, 06 Jun 2011 00:02:07 GMT</pubDate>
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<title>Transcriptome sequencing of an unknown genome</title>
<link>http://www.scientistsolutions.com/t18614-transcriptome+sequencing+of+an+unknown+genome.html</link>
<description><![CDATA[ I am planning to sequence the transcriptome of a genome whose size is around 3.9 gb (whole genome sequence not available), do i go for a 454 first to get a scaffold and then do a illumina sequencing? Please suggest as very few article are available addressing this kind of an experiment.]]></description>
<pubDate>Tue, 10 May 2011 13:26:24 GMT</pubDate>
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<title>No colonies after LR recombination</title>
<link>http://www.scientistsolutions.com/t18382-no+colonies+after+lr+recombination.html</link>
<description><![CDATA[Hello. iam really new to molecular biology. recently, I performed the LR reaction but got no colonies of E.coli. I tried using a new batch of clonase II, leaving the reaction overnight, it didnt work. any suggestions are highly welcome..thanks in advance!<br />]]></description>
<pubDate>Wed, 20 Apr 2011 22:30:09 GMT</pubDate>
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<title>Join online meeting - Mechanism of DNA damage and repair for free</title>
<link>http://www.scientistsolutions.com/t18220-join+online+meeting+_+mechanism+of+dna+damage+and+repair+for+free.html</link>
<description><![CDATA[The purpose of the Mechanism  of DNA Damage and Repair online meeting is to  present and exchange information around the latest discoveries,  methodical approaches, and breakthrough ideas in this field. Learn more from http://targetmeeting.com//Modules/Meetings/MeetingDetails.aspx?Id=17<br />]]></description>
<pubDate>Thu, 31 Mar 2011 16:47:12 GMT</pubDate>
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<title>hdac1 promotes transcription of core neurogenic programme in zfish embryos</title>
<link>http://www.scientistsolutions.com/t17373-hdac1+promotes+transcription+of+core+neurogenic+programme+in+zfish+embryos.html</link>
<description><![CDATA[Harrison MR, Georgiou AS, Spaink HP, Cunliffe VT.  The epigenetic regulator Histone Deacetylase 1 promotes transcription of a core neurogenic programme in zebrafish embryos.  BMC Genomics. 2011 Jan 12;12(1):24. [Epub ahead of print]]]></description>
<pubDate>Mon, 17 Jan 2011 15:43:21 GMT</pubDate>
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<title>synthtic gene design</title>
<link>http://www.scientistsolutions.com/t17214-synthtic+gene+design.html</link>
<description><![CDATA[Hi all,<br /> I am trying to design a syntheic gene which has to be codon optimised for tomato plant. <br />please tell me is there any software or program to design  the gene. steps need to be taken care in designing . <br />thank u in advance<br />]]></description>
<pubDate>Mon, 03 Jan 2011 02:58:34 GMT</pubDate>
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<title>Opinions wanted for an anti-cancer thesis please!</title>
<link>http://www.scientistsolutions.com/t17014-opinions+wanted+for+an+anti_cancer+thesis+please.html</link>
<description><![CDATA[Hi there everyone,<br />I am a master degree student and am interested to do my thesis in the field of cancer, especially in the area of cancer and drug resistance. However, since the field is highly competitive in these days followed by like to find a research niche I came-up with a small hypothesis/plan, but certainly not sure whether it&amp;rsquo;s already established issues and missed to locate the right literatures or whether it might be worth to experiment further with the expensive techniques suc...]]></description>
<pubDate>Fri, 10 Dec 2010 18:48:05 GMT</pubDate>
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<title>Determining the genomic sequences of related fungal strains</title>
<link>http://www.scientistsolutions.com/t16914-determining+the+genomic+sequences+of+related+fungal+strains.html</link>
<description><![CDATA[<br /> 	<br />	<br />	<br />Hello all,<br />So I was asked to come up with an sequencing plan that allows me to determine the genome sequences of <br />a fungal species that has various strains that are pathogenic to either 1 or 2 crops, but not three.<br />(in my case its wheat, barley and corn)<br />the catch is I cant use Sanger method since its so expensive/time consuming<br />Any ideas?<br />thank you,<br />A, from Montreal<br /> <br />]]></description>
<pubDate>Wed, 01 Dec 2010 21:03:43 GMT</pubDate>
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<title>Illumina GAiix available to a good home.</title>
<link>http://www.scientistsolutions.com/t16740-illumina+gaiix+available+to+a+good+home_.html</link>
<description><![CDATA[I have an  Illumina GAIIx System available 2009.  System includes GAIIx, PEMIIx , V 2.8 Software. Please contact me if<br />interested. I am looking to upgrade to Hiseq, or if anyone has an abuncance of ABI 3730xls we can talk about a trade.<br />]]></description>
<pubDate>Tue, 16 Nov 2010 13:07:41 GMT</pubDate>
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<title>Comparison of genome sequences</title>
<link>http://www.scientistsolutions.com/t16135-comparison+of+genome+sequences.html</link>
<description><![CDATA[Well i got two genome sequences at hand, one is a prokaryotic genome and th other one is an eukaryotic genome sequence. Im asked to compare the genome sequence of both to find out the gene size, presence of microsatellites. Can anyone explain me ind etail how to go about with the comparison and i dont have basic knowledge in this. Kindly help me with detailed explanation pleaseeeeeeeeeeeee.]]></description>
<pubDate>Tue, 05 Oct 2010 20:54:06 GMT</pubDate>
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<title>PLEASE explain</title>
<link>http://www.scientistsolutions.com/t15661-please+explain.html</link>
<description><![CDATA[could anyone please explain what does NAT2*5A stand for??<br />i know tht NAT2 is a gene coding for a protein but i've not been able t figure out wat stands for ' * ' followed by a number(eg 5,here) and A???<br />can anyone please explain...<br />NAT2*4 is said to be wild type......i cant understand anything :((<br />please....]]></description>
<pubDate>Mon, 23 Aug 2010 09:18:31 GMT</pubDate>
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<title>The Non-Coding Genome</title>
<link>http://www.scientistsolutions.com/t14845-the+non_coding+genome.html</link>
<description><![CDATA[This symposium will provide an interdisciplinary discussion of the roles of non-coding RNAs with the aim of enhancing our understanding of gene regulation and function.  Topics will include recent discoveries in the fields of prokaryotic and eukaryotic long and short non-coding RNAs.  The functional roles of non-coding RNAs in a wide variety of cell processes will be discussed.]]></description>
<pubDate>Mon, 28 Jun 2010 05:21:31 GMT</pubDate>
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<title>Transcripts Analysis</title>
<link>http://www.scientistsolutions.com/t14794-transcripts+analysis.html</link>
<description><![CDATA[Hi<br />I am working on in vitro expression analysis. I have transfected a mammalian cell line with a gene of wild type and mutant one. surprisingly, I found that the transcript level of the wild type gene was less than the mutant (which is against the logic theory where the wild type should be expressed more than the mutant)..... I wondered what is the reason behind the less expression of the wild type than the mutant one.... any idea because I got exhausted with this without finding an answe...]]></description>
<pubDate>Fri, 18 Jun 2010 10:54:37 GMT</pubDate>
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