{"id":7663,"date":"2017-12-12T12:49:38","date_gmt":"2017-12-12T11:49:38","guid":{"rendered":"http:\/\/www.pologgb.com\/laboratori\/miseq-system-illumina\/"},"modified":"2018-05-02T00:29:50","modified_gmt":"2018-05-01T22:29:50","slug":"miseq-system-illumina","status":"publish","type":"page","link":"https:\/\/www.pologgb.com\/en\/genomica-sequenziamento\/miseq-system-illumina\/","title":{"rendered":"MiSeqDX System &amp; MiSeq System (ILLUMINA)"},"content":{"rendered":"<div class=\"wpb-content-wrapper\">[vc_row][vc_column width=&#8221;1\/4&#8243;][vc_empty_space][vc_btn title=&#8221;&#8221; style=&#8221;outline-custom&#8221; outline_custom_color=&#8221;#002866&#8243; outline_custom_hover_background=&#8221;#002866&#8243; outline_custom_hover_text=&#8221;#ffffff&#8221; shape=&#8221;square&#8221; i_icon_fontawesome=&#8221;fa fa-chevron-left&#8221; add_icon=&#8221;true&#8221; link=&#8221;url:http%3A%2F%2Fwww.pologgb.com%2Fen%2Flaboratori%2Fnextseq-550-system-illumina%2F|title:Previous||&#8221;][vc_btn title=&#8221;&#8221; style=&#8221;outline-custom&#8221; outline_custom_color=&#8221;#002866&#8243; outline_custom_hover_background=&#8221;#002866&#8243; outline_custom_hover_text=&#8221;#ffffff&#8221; shape=&#8221;square&#8221; i_icon_fontawesome=&#8221;fa fa-th-list&#8221; add_icon=&#8221;true&#8221; link=&#8221;url:http%3A%2F%2Fwww.pologgb.com%2Fen%2Flaboratori%2F%232|title:GENOMICS||&#8221;][vc_btn title=&#8221;&#8221; style=&#8221;outline-custom&#8221; outline_custom_color=&#8221;#002866&#8243; outline_custom_hover_background=&#8221;#002866&#8243; outline_custom_hover_text=&#8221;#ffffff&#8221; shape=&#8221;square&#8221; i_align=&#8221;right&#8221; i_icon_fontawesome=&#8221;fa fa-chevron-right&#8221; add_icon=&#8221;true&#8221; link=&#8221;url:http%3A%2F%2Fwww.pologgb.com%2Fen%2Flaboratori%2Fhiseq-2500-system-illumina%2F|title:Next||&#8221;][\/vc_column][vc_column width=&#8221;3\/4&#8243;][vc_empty_space height=&#8221;26px&#8221;][vc_custom_heading text=&#8221;MiSeqDX System &amp; MiSeq System (ILLUMINA)&#8221; font_container=&#8221;tag:h1|text_align:right|color:%23002866&#8243; use_theme_fonts=&#8221;yes&#8221;][\/vc_column][\/vc_row][vc_row full_width=&#8221;stretch_row&#8221; equal_height=&#8221;yes&#8221; css=&#8221;.vc_custom_1513016386462{background-color: #1f314d !important;}&#8221;][vc_column][vc_column_text]<span style=\"color: #ffffff;\">The MiSeq System offers the first end-to-end sequencing solution, integrating cluster generation, amplification, sequencing, and data analysis into a single instrument.<br \/>\nMiSeq is the only benchtop sequencer that can produce 2 x 300 paired-end reads and up to 15 Gb of data in a single run. This allows assembly of small genomes or detection of target variants with unmatched accuracy, especially within homopolymer regions. Now, even more samples can be processed in less time while generating more reads per run than any previous versions.<\/span><\/p>\n<p><span style=\"color: #ffffff;\">The MiSeq System offers a cost-effective alternative to capillary electrophoresis (CE) for applications such as targeted resequencing, clone checking, and amplicon sequencing.<\/span><\/p>\n<p><span style=\"color: #ffffff;\">The MiSeqDx System is the first NGS platform to receive FDA clearance for in vitro diagnostic (IVD) testing.<\/span>[\/vc_column_text][vc_row_inner equal_height=&#8221;yes&#8221; content_placement=&#8221;middle&#8221; gap=&#8221;30&#8243;][vc_column_inner width=&#8221;1\/2&#8243;][vc_custom_heading text=&#8221;Most Frequent Applications&#8221; font_container=&#8221;tag:h3|text_align:left|color:%234cadc9&#8243; use_theme_fonts=&#8221;yes&#8221;][vc_separator color=&#8221;white&#8221;][vc_column_text]<span style=\"color: #ffffff;\">Small genome sequencing, 16S\/18S metagenomics, smallRNA sequencing, HLA sequencing, preimplantation genetic screening (PGS), and preimplantation genetic diagnosis (PGD), cystic fibrosis, amplicon sequencing.<\/span>[\/vc_column_text][vc_empty_space height=&#8221;40px&#8221;][vc_custom_heading text=&#8221;Highlights&#8221; font_container=&#8221;tag:h3|text_align:left|color:%234cadc9&#8243; use_theme_fonts=&#8221;yes&#8221;][vc_separator color=&#8221;white&#8221;][vc_column_text]\n<h4><span style=\"color: #ffffff;\">Multiplex up to 96 samples per run for greater efficiency<\/span><\/h4>\n<h4><span style=\"color: #ffffff;\">Get accurate bi-directional amplicon sequencing<\/span><\/h4>\n<h4><span style=\"color: #ffffff;\">Generate more complete de novo assemblies for small genome<\/span><\/h4>\n[\/vc_column_text][\/vc_column_inner][vc_column_inner width=&#8221;1\/2&#8243;][vc_single_image image=&#8221;6698&#8243; img_size=&#8221;full&#8221; alignment=&#8221;center&#8221; style=&#8221;vc_box_outline&#8221; border_color=&#8221;white&#8221; onclick=&#8221;link_image&#8221;][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row][vc_row][vc_column][vc_empty_space height=&#8221;20px&#8221;][vc_custom_heading text=&#8221;Technical Specifications&#8221; font_container=&#8221;tag:h3|text_align:left|color:%23002866&#8243; use_theme_fonts=&#8221;yes&#8221;][vc_table vc_table_theme=&#8221;simple_purple&#8221;][align-left],[align-center],[align-center],[align-center]MiSeq%20%20Reagent%20kit%20v3,[align-center]MiSeq%20%20Reagent%20kit%20v2,[align-center]MiSeq%20%20Reagent%20kit%20v2%20Micro,[align-center]MiSeq%20%20Reagent%20kit%20v2%20Nano|[align-left],[align-center],[align-center],[align-center]No.%20of%20Samples%20%2F%20Time,[align-center]No.%20of%20Samples%20%2F%20Time,[align-center]No.%20of%20Samples%20%2F%20Time,[align-center]No.%20of%20Samples%20%2F%20Time|[align-left]Amplicon%20Resequencing,[align-center]%3E250X%20Coverage%20,[align-center]2x150bp,[align-center]96%20%2F%2028%20Hours,[align-center]96%20%2F%2024%20Hours,[align-center]96%20%2F%2019%20Hours,[align-center]96%20%2F%2017%20Hours|[align-left]16S%20Metagenomics%20,[align-center]1M%20Reads,[align-center]2x250bp,[align-center]40%20%2F%2047%20Hours,[align-center]20%20%2F%2039%20Hours,[align-center],[align-center]2%20%2F%2028%20Hours|[align-left]Small-Genome%20Sequencing,[align-center]%3E30X%20Coverage,[align-center]2x250bp,[align-center]72%20%2F%2047%20Hours,[align-center]48%20%2F%2039%20Hours,[align-center],[align-center]3%20%2F%2028%20Hours|[align-left]Small%20RNA%20Sequencing,[align-center]1M%20Reads,[align-center]1x36bp,[align-center],[align-center]12%20%2F%204%20Hours,[align-center],[align-center]|[align-left]Library%20Quality%20Control%20,[align-center]0%2C5M%20Reads,[align-center]2x25bp,[align-center],[align-center]48%20%2F%205%2C5%20Hours,[align-center],[align-center][\/vc_table][vc_empty_space height=&#8221;50px&#8221;][\/vc_column][\/vc_row]\n<\/div>","protected":false},"excerpt":{"rendered":"<p>[vc_row][vc_column width=&#8221;1\/4&#8243;][vc_empty_space][vc_btn title=&#8221;&#8221; 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