<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-05-30T13:00:01Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/11578" metadataPrefix="marc">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/11578</identifier><datestamp>2026-02-03T12:48:29Z</datestamp><setSpec>com_10630_4046</setSpec><setSpec>com_10630_10</setSpec><setSpec>col_10630_11575</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">dc</subfield>
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      <subfield code="a">Cabrera-Mulero, Amanda</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">Alba-Bernal, Alfonso</subfield>
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      <subfield code="c">2016-06-07</subfield>
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      <subfield code="a">The Next Generation Sequencing (NGS) allows to sequence the whole genome of an&#xd;
organism, compared to Maxam and Gilbert and Sanger sequencing that only allow to&#xd;
sequence, hardly, a single gene. Removing the separation of DNA fragments by&#xd;
electrophoresis, and the development of techniques that let the parallelization (analysing&#xd;
simultaneously several DNA fragments) have been crucial for the improvements of this&#xd;
process. The new companies in this ambit, Roche and Illumina, bet for different protocols to&#xd;
achieve these goals. Illumina bets for the sequencing by synthesis (SBS), requiring the library&#xd;
preparation and the use of adapters. Likewise, Illumina has replaced Roche because its lower&#xd;
rate of misincorporation, making it ideal for studies of genetic variability, transcriptomic,&#xd;
epigenomic, and metagenomic, in which this study will focus.&#xd;
However, it is noteworthy that the last progress in sequencing is carried out by the third&#xd;
generation sequencing, using nanotechnology to design small sequencers that sequence the&#xd;
whole genome of an organism quickly and inexpensively. Moreover, they provide more&#xd;
reliable data than current systems because they sequence a single molecule, solving the&#xd;
problem of synchronisation. In this way, PacBio and Nanopore allow a great progress in&#xd;
diagnostic and personalized medicine.&#xd;
Metagenomics provide to make a qualitative and quantitative analysis of the various species&#xd;
present in a sample. The main advantage of this technique is the no necessary isolation and&#xd;
growth of the species, allowing the analysis of nonculturable species. The Illumina protocol&#xd;
studies the variable regions of the 16S rRNA gene, which contains variable and not variables&#xd;
regions providing a phylogenetic classification. Therefore, metagenomics is a topic of&#xd;
interest to know the biodiversity of complex ecosystems and to study the microbiome of&#xd;
patients given the high involvement with certain microbial profiles on the condition of&#xd;
certain metabolic diseases.</subfield>
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      <subfield code="a">http://hdl.handle.net/10630/11578</subfield>
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      <subfield code="a">Genómica</subfield>
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      <subfield code="a">NGS y Metagenómica</subfield>
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