Secuenciación do ADN: Diferenzas entre revisións
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== Métodos en desenvolvemento ==
DNA sequencing methods currently under development include labeling the DNA polymerase,<ref>{{cite web|url=http://visigenbio.com/technology_overview.html|title=VisiGen Biotechnologies Inc. – Technology Overview |publisher=Visigenbio.com |date= |accessdate=2009-11-15}}</ref> reading the sequence as a DNA strand transits through [[nanopore sequencing|nanopores]],<ref>{{cite web|url=http://mcb.harvard.edu/branton/index.htm |title=The Harvard Nanopore Group |publisher=Mcb.harvard.edu|date= |accessdate=2009-11-15}}</ref><ref name="Physorg">{{cite web |url=http://www.physorg.com/news157378086.html |title=Nanopore Sequencing Could Slash DNA Analysis Costs |work= |accessdate=}}</ref> and microscopy-based techniques, such as [[Atomic force microscope|atomic force microscopy]] or [[Transmission electron microscopy DNA sequencing|transmission electron microscopy]] that are used to identify the positions of individual nucleotides within long DNA fragments (>5,000 bp) by nucleotide labeling with heavier elements (e.g., halogens) for visual detection and recording.<ref>
Third generation technologies aim to increase throughput and decrease the time to result and cost by eliminating the need for excessive reagents and harnessing the processivity of DNA polymerase.<ref>{{cite journal|last=Schadt|first=E.E.|coauthors=S. Turner, A. Kasarskis|title=A window into third-generation sequencing|journal=Human Molecular Genetics|year=2010|volume=19|issue=R2|pages=R227–40|doi=10.1093/hmg/ddq416|pmid=20858600}}</ref>
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