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	<title><![CDATA[BOL: All site news]]></title>
	<link>https://bioinformaticsonline.com/news/all?offset=10</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/42370/ncbi-blast-have-added-new-columns-to-the-descriptions</guid>
	<pubDate>Tue, 01 Dec 2020 09:56:07 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/42370/ncbi-blast-have-added-new-columns-to-the-descriptions</link>
	<title><![CDATA[NCBI BLAST have added new columns to the Descriptions]]></title>
	<description><![CDATA[<p><span>NCBI BLAST have added new columns to the Descriptions Table for web BLAST output. The new columns are&nbsp; Scientific Name, Common Name, Taxid, and Accession Length. Common Name and Accession Length are now part of the default display. You can click 'Select columns' or 'Manage columns' to add or remove columns from the display Your preferences will be saved for your next visit to BLAST, and when you download your results, whatever columns you have displayed will be saved. See the NCBI Insights post (</span><a href="https://go.usa.gov/x7fPE" target="_blank">https://go.usa.gov/x7fPE</a><span>) for more details.</span></p>]]></description>
	<dc:creator>Neel</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/42325/published-a-dataset-of-363-genomes-from-approximately-92-percent-of-bird-families</guid>
	<pubDate>Thu, 19 Nov 2020 07:04:41 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/42325/published-a-dataset-of-363-genomes-from-approximately-92-percent-of-bird-families</link>
	<title><![CDATA[Published a dataset of 363 genomes from approximately 92 percent of bird families]]></title>
	<description><![CDATA[<div>A research team published a dataset of 363 genomes from approximately 92 percent of bird families and showed the significance of sampling dense organisms for biodiversity research. The study was jointly conducted by Chinese and international institutions and museums and was led by researchers from the Kunming Institute of Zoology (KIZ) of the Chinese Academy of Sciences (CAS). Total of 267 were newly published among the 363 sequenced genomes.&nbsp;They were mainly taken from samples of avian tissue kept in museums around the world, enabling researchers to sequence rare and endangered birds' genomes.</div><div>&nbsp;</div><div>Its descendants have adapted to a wide variety of ecological niches since the first bird formed more than 150 million years ago, giving rise to small, hovering hummingbirds, plunge-diving pelicans and showy paradise birds. More than 10,000 bird species live on the planet today - and now scientists are well on their way to capturing a full genetic image of that diversity.</div><div>&nbsp;</div><div>B10K is expanding its efforts to encompass the next stage of avian classification with 363 genomes complete. The team will sequence thousands of extra genomes in this process, attempting to represent each of the approximately 2,300 bird genera.</div><div>&nbsp;</div><div><img src="https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41586-020-2873-9/MediaObjects/41586_2020_2873_Fig1_HTML.png?as=webp" alt="image" style="border: 0px;"></div><div>&nbsp;</div><div>The genomic resource is expected to provide new insights on evolutionary processes in cross-species comparative studies and assist in efforts to protect species, according to the research findings reported as a cover story in the journal Nature.</div><div>&nbsp;</div><div>Ref at&nbsp;Dense sampling of bird diversity increases power of comparative genomics&nbsp;https://www.nature.com/articles/s41586-020-2873-9</div>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/42324/comparative-genomics-data-set-including-240-mammals-released</guid>
	<pubDate>Thu, 19 Nov 2020 06:45:39 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/42324/comparative-genomics-data-set-including-240-mammals-released</link>
	<title><![CDATA[Comparative Genomics Data Set Including 240 Mammals Released !]]></title>
	<description><![CDATA[<p>The genome of 130 mammals was sequenced by a large international consortium and the data was analyzed together with 110 existing genomes to allow scientists to identify the important positions in the DNA. This report, published in Nature today will help advance research on human disease mutations and inform how best to protect endangered species.</p><p>In addition to the knowledge of the human genome, all these genomes, widely sampled across mammals, can be used to research how particular organisms respond to different conditions. Some otters, for example, have a thick, water-resistant shell, and some rodents, but not all, have adapted to hibernation. These animal traits will help us to understand human traits, such as metabolic diseases.</p><p><img src="https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41586-020-2876-6/MediaObjects/41586_2020_2876_Fig1_HTML.png?as=webp" alt="image" style="border: 0px; border: 0px;"></p><p>With climate change and more animal ecosystems being threatened by human activity, the protection of endangered species is becoming increasingly important. Scientists have historically researched several people in various populations of a species to understand the genetic variation that occurs in that species. This is important for understanding how particular species can be protected. In this study, animals on the Red List of Endangered Species of the International Union for Conservation of Nature had fewer differences in their genomes, which is consistent with their endangered status.</p><p>Ref @&nbsp;A comparative genomics multitool for scientific discovery and conservation&nbsp;https://www.nature.com/articles/s41586-020-2876-6</p><p>&nbsp;Data at&nbsp;http://zoonomiaproject.org/</p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/42319/blast-2110-release-is-now-available-on-ftp-site</guid>
	<pubDate>Sat, 14 Nov 2020 21:37:53 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/42319/blast-2110-release-is-now-available-on-ftp-site</link>
	<title><![CDATA[BLAST+ 2.11.0 release is now available on FTP site !]]></title>
	<description><![CDATA[<p><span style="font-size: 12.8px;"></span><span style="font-size: 12.8px;">BLAST+ 2.11.0 release is now available from our FTP site. The main advance is the ability to provide usage reports to NCBI to help us improve BLAST. This information is limited to the name of the BLAST program, some basic database metadata, a few BLAST parameters, as well the number and total size of your queries. See the Privacy document for more details on the information we collect, how we will use it, and how you can opt-out of reporting.</span></p><div><div><div><div lang="EN-US"><div><p>Another new feature allows threading by query batch in rpsblast/rpstblastn. Enabling this option using -m t provides more efficient searching with large numbers of queries. &nbsp;See release notes for details on more improvements and bug fixes.</p><p>Useful Links<br />------------<br />NCBI Insights:&nbsp;<a href="https://ncbiinsights.ncbi.nlm.nih.gov/2020/11/12/blast-2-11-0/" target="_blank">https://ncbiinsights.ncbi.nlm.nih.gov/2020/11/12/blast-2-11-0/</a></p><p>BLAST FTP:&nbsp;<a href="https://go.usa.gov/x7QQ3" target="_blank">https://go.usa.gov/x7QQ3</a><br />Privacy document:&nbsp;<a href="https://go.usa.gov/x7QQe" target="_blank">https://go.usa.gov/x7QQe</a><br />Release notes:&nbsp;<a href="https://go.usa.gov/x7Qnv" target="_blank">https://go.usa.gov/x7Qnv</a></p></div></div></div></div></div>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/42306/ramalingaswami-re-entry-fellowship</guid>
	<pubDate>Tue, 10 Nov 2020 04:37:23 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/42306/ramalingaswami-re-entry-fellowship</link>
	<title><![CDATA[Ramalingaswami Re-entry Fellowship]]></title>
	<description><![CDATA[<div dir="auto">Last date approaching soon!</div><div><div dir="auto">Ramalingaswami Re-entry <span><a href="https://www.facebook.com/hashtag/fellowship?__eep__=6&amp;__cft__[0]=AZXzYVrS9hztPYuy8ki1opvetM7YkyqF784LJ7WmUtQUbmLjURP3B7o73PhEUz2H3LhYSAjM8O2nWs_-JmImmKbtpEZmiOnQJpeW9sS5DDIrb3kR9gfNn9C6KfExYoYkmpSeyWTsg8S3EKQwiFpnDbGOBwFc1LYL7H5oVp7JeVIxQB2Y3MiFv0-X9WPYZB0NbqI&amp;__tn__=*NK-R">#Fellowship</a></span> 2020-2021 for Indian Nationals to pursue their R&amp;D interests in Indian institutions.</div></div><div><div dir="auto">Deadline: November 15, 2020</div></div><div><div dir="auto">For more information: <span><a href="http://dbtindia.gov.in/latest-announcement/advertisement-ramalingaswami-re-entry-fellowship-2020-21" target="_blank">http://dbtindia.gov.in/.../advertisement-ramalingaswami...</a></span></div></div>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/42296/igblast-117-is-now-available-with-improved-identification-of-productive-v-gene-sequences</guid>
	<pubDate>Sun, 01 Nov 2020 16:52:58 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/42296/igblast-117-is-now-available-with-improved-identification-of-productive-v-gene-sequences</link>
	<title><![CDATA[IgBLAST 1.17 is now available with improved identification of productive V gene sequences]]></title>
	<description><![CDATA[<p>A new release of&nbsp;<a href="https://go.usa.gov/x7WMc" target="_blank">IgBLAST</a>&nbsp;(1.17), the popular package for classifying and analyzing immunoglobulin and T cell receptor sequences, is now available on the&nbsp;<a href="https://go.usa.gov/x7WMc" target="_blank">web</a>&nbsp;and from the&nbsp;<a href="https://ftp.ncbi.nih.gov/blast/executables/igblast/release/LATEST" target="_blank">FTP site</a>. The updated package is better at identifying productive V gene sequences. We added a new field , &ldquo;V frame shift&rdquo;, to the IgBLAST output to indicate whether the V gene translation frame contains a frame-shift. We have also updated the definition of a productive V(D)J sequence to now exclude those with internal frame shifts.</p><p>See the&nbsp;<a href="https://ncbi.github.io/igblast/" target="_blank">new IgBLAST manual</a>&nbsp;on the NCBI GitHub site for more information on setting up and running IgBLAST.</p><p>If you have any questions or concerns, please email us at&nbsp;<a href="mailto:blast-help@ncbi.nlm.nih.gov" target="_blank">blast-help@ncbi.nlm.nih.gov</a></p><p>&nbsp;</p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/42196/the-pandemic-has-worsened-the-plight-of-postdoctoral-researchers</guid>
	<pubDate>Fri, 11 Sep 2020 11:19:42 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/42196/the-pandemic-has-worsened-the-plight-of-postdoctoral-researchers</link>
	<title><![CDATA[The pandemic has worsened the plight of postdoctoral researchers !]]></title>
	<description><![CDATA[<p><em>The pandemic has worsened the plight of postdoctoral researchers. Funders need to be offering more than moral support.</em></p><p><em><a href="https://www.nature.com/" target="_blank">Nature</a></em>&nbsp;conducted a poll ran in June and July, and more than 7,600 people responded from across 19 disciplines. The sample, a self-selecting group scattered over 93 countries, is not fully representative globally, because the overwhelming majority of respondents are in Europe and North America. But the picture that emerges is undoubtedly concerning.&nbsp;</p><p>Six out of ten respondents think the pandemic has worsened their career prospects, and one in four feel that their supervisors have not done enough to support them during the pandemic. Moreover, 23% of respondents said that they have sought help for anxiety or depression caused by their work, and a further 26% would like such help but have not yet sought it. This is in line with other findings of pandemic-related mental ill-health.</p><p>Reference:</p><p>https://media.nature.com/original/magazine-assets/d41586-020-02541-9/d41586-020-02541-9.pdf</p>]]></description>
	<dc:creator>BioStar</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/42141/dbt-biotechnology-eligibility-test-bet-2020</guid>
	<pubDate>Fri, 21 Aug 2020 09:17:24 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/42141/dbt-biotechnology-eligibility-test-bet-2020</link>
	<title><![CDATA[DBT BIOTECHNOLOGY ELIGIBILITY TEST (BET) 2020]]></title>
	<description><![CDATA[<p><span>Ministry of Science &amp;Technology, Govt. of India</span></p><p><span>DBT-Junior Research Fellowship (DBT-JRF) in Biotechnology (2020)</span></p><p><span><span>BIOTECHNOLOGY ELIGIBILITY TEST (BET) 2020</span></span></p><p>Applications are invited from bonafide Indian citizens, residing in India for award of &ldquo;DBT-Junior Research Fellowship&rdquo; (DBT-JRF) for pursuing research in frontier areas of Biotechnology and Life Sciences. The candidates will be selected through &ldquo;Biotechnology Eligibility Test (BET)&rdquo;. Based on the performance in BET, two categories of merit list will be prepared (Category-I and Category-II). Government of India norms for reservation will be followed for selection. Candidates selected under category-I will be eligible to avail fellowship under the programme. These will be tenable at any University/Institute in India where the selected candidate registers for PhD Programme. Candidates selected under Category-II will be eligible to be appointed in any DBT sponsored project and avail fellowship from the project equivalent to NET/GATE, subject to selection through institutional selection process. There will be no binding on Principal Investigators of DBT sponsored projects to select JRF for their project from category-II list. Selection in category-II will not entitle student for any fellowship from DBT-JRF programme.</p><p><span>ELIGIBILITY</span></p><p><span>Qualification</span>: M.Sc./ M.Tech./ M.V.Sc. or equivalent degree/ Integrated BS-MS/ B.E./ B.Tech. in any discipline of&nbsp;<a href="https://www.biotecnika.org/category/jobs/biotech-jobs/">Biotechnology</a>, M.Sc./ M.Tech. Bioinformatics/ Computational Biology, students admitted under DBT supported Postgraduate Teaching Programs. M.Sc. Life Science/ Bioscience/ Zoology/ Botany/ Microbiology/ Biochemistry/ Biophysics and Masters in Allied areas of Biology/Life Sciences. Candidates appearing in the final year examination are also eligible to apply.</p><p><span>Marks</span>: Minimum 60% marks for General, EWS &amp; OBC category and 55% for SC/ ST/ Differently abled in aggregate (or equivalent grade).</p><p><span>Age Limit</span>: Upto 28 years as on the last date of application for General &amp; EWS category. Age relaxation of up to 5 years (33 years) for SC/ ST/ Differently Abled/ women candidates and upto 3 years (31 years) for OBC (Non-Creamy Layer) candidates.</p><p>For detailed procedure for filling the application form, payment of application fee and uploading of required documents/ certificates in the prescribed format, please visit:&nbsp;<span><a href="http://rcb.res.in/BET2020" target="_blank">http://rcb.res.in/BET2020</a></span>. A non-refundable and non-transferable application fee of Rs. 1000/-is payable online by General/ OBC/ EWS candidates and Rs 250/- by SC/ ST/ Differently abled candidates.</p><p><span>IMPORTANT DATES</span></p><table width="691">
<tbody>
<tr>
<td>Online Registration Start</td>
<td><span>April 20, 2020</span></td>
</tr>
<tr>
<td>Online Registration Close</td>
<td><span>May 18, 2020</span></td>
</tr>
<tr>
<td>BET 2020</td>
<td><span>June 30, 2020 (Tuesday)* Tentative</span></td>
</tr>
<tr>
<td>Display of question paper and answer key on website</td>
<td><span>June 30, 2020</span></td>
</tr>
<tr>
<td>Last date of accepting representation of any discrepancy in Question paper &amp; Answer key</td>
<td><span>July 03, 2020</span></td>
</tr>
<tr>
<td>Declaration of BET 2020 Result</td>
<td><span>July 20, 2020</span></td>
</tr>
</tbody>
</table>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/42023/encode3-a-collection-of-research-articles-and-related-content-describing-the-encyclopedia-of-dna-elements-its-datasets-and-tools</guid>
	<pubDate>Sat, 08 Aug 2020 08:25:21 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/42023/encode3-a-collection-of-research-articles-and-related-content-describing-the-encyclopedia-of-dna-elements-its-datasets-and-tools</link>
	<title><![CDATA[ENCODE3: A collection of research articles and related content describing the Encyclopedia of DNA Elements, its datasets and tools.]]></title>
	<description><![CDATA[<p>How cells, tissues and organisms interpret the information encoded in the genome has vital implications for our understanding of development, health and disease. Launched in 2003, the ENCyclopedia Of DNA Elements (ENCODE) project has the aim of mapping the functional elements in the human genome (later expanded to include model organisms).</p><p>During the first phase of ENCODE, published in 2007, microarray-based technologies were used to detect regions associated with transcription factors, certain histone modifications and open chromatin within a pre-specified 1% of the human genome.</p><p>ENCODE&rsquo;s second phase saw a switch to sequencing-based technologies, the addition of new assay types and the analysis of functional elements genome-wide, described in a collection of research articles in 2012.</p><p><span>The&nbsp;</span><a href="https://www.nature.com/articles/s41586-020-2493-4">Encyclopedia paper of ENCODE 3</a><span>, published in&nbsp;</span><em>Nature</em><span>, gives an overview of the various assays that were performed in human and mouse cell lines and tissues and describes a Registry of human and mouse candidate&nbsp;</span><em>cis</em><span>-regulatory elements (cCREs).</span></p><p>More at&nbsp;<a href="https://www.nature.com/immersive/d42859-020-00027-2/index.html">https://www.nature.com/immersive/d42859-020-00027-2/index.html</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/41956/blast-on-docker-google-cloud-amazon-cloud</guid>
	<pubDate>Thu, 09 Jul 2020 02:57:11 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/41956/blast-on-docker-google-cloud-amazon-cloud</link>
	<title><![CDATA[Blast on Docker, Google Cloud, Amazon Cloud]]></title>
	<description><![CDATA[<p>As announced in a&nbsp;<a href="https://ncbiinsights.ncbi.nlm.nih.gov/2019/07/16/the-blast-programs-and-databases-are-available-in-docker-and-cloud-ready/" target="_blank">previous post</a>, we offer a&nbsp;<a href="https://www.docker.com/" target="_blank">Docker</a>&nbsp;version of NCBI BLAST+ that you can use locally or on the&nbsp;<a href="https://cloud.google.com/" target="_blank">Google Cloud</a>&nbsp;where we have pre-loaded BLAST databases.&nbsp; We are happy to announce that the same functionality is now available on the&nbsp;<a href="https://aws.amazon.com/" target="_blank">Amazon Cloud</a>.&nbsp; In addition, we now offer 23 different BLAST databases on each cloud platform.<span style="text-decoration: underline;"></span><span style="text-decoration: underline;"></span></p><p>As mentioned before, working with BLAST+ in Docker and the cloud has several advantages:<span style="text-decoration: underline;"></span><span style="text-decoration: underline;"></span></p><ul>
<li>Docker manages installation and maintenance of the BLAST programs and databases.<span style="text-decoration: underline;"></span><span style="text-decoration: underline;"></span></li>
<li>Docker makes it is easier to integrate BLAST with other tools in your pipelines.<span style="text-decoration: underline;"></span><span style="text-decoration: underline;"></span></li>
<li>NCBI BLAST databases are pre-loaded now on the both the&nbsp;<a href="https://cloud.google.com/" target="_blank" title="Follow link">Google Cloud</a>&nbsp;and&nbsp;<a href="https://aws.amazon.com/" target="_blank" title="Follow link">Amazon Cloud</a>, providing fast access.<span style="text-decoration: underline;"></span><span style="text-decoration: underline;"></span></li>
</ul><p>You can also use the BLAST+ Docker image on any Docker-enabled platform, such as another cloud platform or on your local computer.<span style="text-decoration: underline;"></span><span style="text-decoration: underline;"></span></p><p>See the&nbsp;&nbsp;<a href="https://github.com/ncbi/blast_plus_docs" target="_blank" title="Follow link">BLAST+ in the Cloud</a>&nbsp;and&nbsp;&nbsp;<a href="https://github.com/ncbi/docker/wiki/Getting-BLAST-databases" target="_blank" title="Follow link">database information</a>&nbsp;documentation to get started.<span style="text-decoration: underline;"></span><span style="text-decoration: underline;"></span></p><p>If you have any questions, please email us at&nbsp;blast-help@ncbi.nlm.nih.gov</p><p>Source:<span>Dave Arndt</span></p>]]></description>
	<dc:creator>LEGE</dc:creator>
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