{"id":64156,"date":"2015-04-02T05:44:12","date_gmt":"2015-04-02T09:44:12","guid":{"rendered":"http:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/longer-dna-fragments-reveal-rare-species-diversity\/"},"modified":"2015-04-02T05:44:12","modified_gmt":"2015-04-02T09:44:12","slug":"longer-dna-fragments-reveal-rare-species-diversity","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/genome\/longer-dna-fragments-reveal-rare-species-diversity\/","title":{"rendered":"Longer DNA Fragments Reveal Rare Species Diversity"},"content":{"rendered":"<p><p>Contact Information         <\/p>\n<p>      Available for logged-in reporters only    <\/p>\n<p>    Newswise  Many microbes cannot be cultivated in a laboratory    setting, hindering attempts to understand Earths microbial    diversity. Since microbes are heavily involved in, and    critically important to environmental processes from nutrient    recycling, to carbon processing, to the fertility of topsoils,    to the health and growth of plants and forests, accurately    characterizing them, as a basis for understanding their    activities, is a major goal of the Department of Energy (DOE).    One approach has been to study collected DNA extracted from the    complex microbial community, or the metagenome, in order to    describe its DNA-coded parts catalog and understand how    microbes respond and adapt to environmental changes. Studying a    population rather than an individual raises different obstacles    on the path to knowledge. The challenges of assembling genes    and genomic fragments into meaningful sequence information for    an unknown microbe has been likened to putting together a    jigsaw puzzle without knowing what the final picture should    look like, or even if you have all the pieces.  <\/p>\n<p>    For metagenomics, said Jillian Banfield of the University of    California, Berkeley and Lawrence Berkeley National    Laboratorys Earth Sciences Division, a longtime collaborator    of the DOE Joint Genome Institute (DOE JGI), a DOE Office of    Science User Facility, it is like reconstructing puzzles from    a mixture of pieces from many different puzzlesand not knowing    what any of them look like. Part of the problem lies in the    fact that the more commonly used sequencing machines generate    data in short lengths or fragments, on the order of a few    hundred base pairs of DNA. Additionally, short-read assemblers    may not be able to distinguish among multiple occurrences of    the same or similar sequences and will therefore either fail to    place them in the correct context, or eliminate them entirely    from the final assembly, in the same way that putting together    a jigsaw puzzle with many small pieces that look the same, is    difficult. The result of this are gaps that indicate not all of    the microbes in a community can be identified through the    application of environmental genomics.  <\/p>\n<p>    In a study published on the cover of the April 2015    edition of Genome Research, a team including DOE JGI    and Berkeley Lab researchers compared two ways of using the    next generation Illumina sequencing machines, one of    which--TruSeq Synthetic Long-Reads--produced significantly    longer reads than the other. Metagenome data were generated    from the Berkeley Lab-led DOE subsurface biogeochemistry field    study site in Rifle, Colorado by a Banfield-led team. They    evaluated the accuracy of the genomes reconstructed from the    sequences produced by the two Illumina technologies to learn    more about the microbes present in lower amounts than others    and better determine the species richness of the metagenome    samples.  <\/p>\n<p>    The project is part of the Berkeley Lab Genomes-to-Watershed Scientific    Focus Area (SFA), which involves over 50 scientists from    Berkeley Lab and other institutions including UC Berkeley,    Pacific Northwest National Laboratory, Colorado School of    Mines, and Oak Ridge National Laboratory. The    Genomes-to-Watershed SFA is led by geophysicist Susan Hubbard,    the director of Berkeley Labs Earth Sciences Division. Its    goal is to develop an approach for gaining a predictive    understanding of complex, biologically based system    interactions from the genome to the watershed scale. Jill    Banfield is a co-lead of the Metabolic Potential component of this team    project, which focuses on characterizing prevalent metabolic    pathways in subsurface microbial communities that mediate    carbon and electron flux, and using that information to inform    genome-enabled watershed reactive transport simulators.    Banfield describes the Metabolic Potential component of the SFA    effort in this video, and some of her groups other recent    groundbreaking subsurface ecogenomic findings associated with    this project can be found here.  <\/p>\n<p>    Revisiting Microbial Communities in Rifle, Colorado  <\/p>\n<p>    For the study, the team used sediment samples collected from an    aquifer adjacent to the Colorado River, which had been used for    previous experiments. For one of these earlier efforts the DOE JGI    sequenced Rifle Site microbial communities and was able to    completely reconstruct a high quality genome of a previously    unknown organism from short-read assemblies. Additionally, the    findings revealed that many of the bacteria and archaea found    in the samples had not been previously recognized or sampled.  <\/p>\n<p>    For their study, the researchers compared the sequences and    assemblies generated from Illuminas short read technology with    the data from the newer, longer-read technology that generates    read lengths of up around 8,000 base pairs. They found that the    longer reads captured more of the communitys diverse species.    For instance, using short read technology, they previously    identified just over 160 microbial species within a sediment    sample. Using the longer-read technology, though, over 400    microbial species from the sample could be phylogenetically    classified, though some accounted for just 0.1 percent of the    community.  <\/p>\n<p>    The studys first author, Itai Sharon of UC Berkeley, pointed    out that they also identified species that previously failed to    assemble due to the presence of closely related species within    the sample. These close relatives, accounting for as much as 15    percent of the community, confounded the assembly algorithm.    These populations were pretty much missed by the short read    assemblies because assemblers tend to fail at the presence of    multiple closely related species and strains. Using algorithms    that we developed for analyzing the long reads we were able to    reconstruct genome architecture for these populations, he    said.  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Originally posted here:<br \/>\n<a target=\"_blank\" href=\"http:\/\/www.newswise.com\/articles\/view\/632009\/?sc=rssn\/RK=0\/RS=NXX3fSqm908MYUECvb2wbkjF7KM-\" title=\"Longer DNA Fragments Reveal Rare Species Diversity\">Longer DNA Fragments Reveal Rare Species Diversity<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Contact Information Available for logged-in reporters only Newswise Many microbes cannot be cultivated in a laboratory setting, hindering attempts to understand Earths microbial diversity. Since microbes are heavily involved in, and critically important to environmental processes from nutrient recycling, to carbon processing, to the fertility of topsoils, to the health and growth of plants and forests, accurately characterizing them, as a basis for understanding their activities, is a major goal of the Department of Energy (DOE).  <a href=\"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/genome\/longer-dna-fragments-reveal-rare-species-diversity\/\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[25],"tags":[],"class_list":["post-64156","post","type-post","status-publish","format-standard","hentry","category-genome"],"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/64156"}],"collection":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/comments?post=64156"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/64156\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/media?parent=64156"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/categories?post=64156"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/tags?post=64156"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}