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90
Rubicon Genomics paired-end sequencing library construction kits thruplex
Paired End Sequencing Library Construction Kits Thruplex, supplied by Rubicon Genomics, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/paired-end sequencing library construction kits thruplex/product/Rubicon Genomics
Average 90 stars, based on 1 article reviews
paired-end sequencing library construction kits thruplex - by Bioz Stars, 2026-04
90/100 stars
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90
Rubicon Genomics thruplex fragmented dna prep kit thruplex-fd
Two <t>DNA</t> samples (Test DNA 1 and Test DNA 2) were subjected to four exome sequencing (ES) protocols performed in parallel: control (Standard ES) and three modified (REPLI-g ES, GenomePlex ES and <t>ThruPLEX-FD</t> ES). Common steps performed in parallel for several protocols are shown by text boxes spanning the corresponding number of protocol columns.
Thruplex Fragmented Dna Prep Kit Thruplex Fd, supplied by Rubicon Genomics, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/thruplex fragmented dna prep kit thruplex-fd/product/Rubicon Genomics
Average 90 stars, based on 1 article reviews
thruplex fragmented dna prep kit thruplex-fd - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

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Two DNA samples (Test DNA 1 and Test DNA 2) were subjected to four exome sequencing (ES) protocols performed in parallel: control (Standard ES) and three modified (REPLI-g ES, GenomePlex ES and ThruPLEX-FD ES). Common steps performed in parallel for several protocols are shown by text boxes spanning the corresponding number of protocol columns.

Journal: PLoS ONE

Article Title: Exome Sequencing from Nanogram Amounts of Starting DNA: Comparing Three Approaches

doi: 10.1371/journal.pone.0101154

Figure Lengend Snippet: Two DNA samples (Test DNA 1 and Test DNA 2) were subjected to four exome sequencing (ES) protocols performed in parallel: control (Standard ES) and three modified (REPLI-g ES, GenomePlex ES and ThruPLEX-FD ES). Common steps performed in parallel for several protocols are shown by text boxes spanning the corresponding number of protocol columns.

Article Snippet: One library was prepared starting from 10 ng of sheared original DNA using ThruPLEX Fragmented DNA Prep kit (ThruPLEX-FD) from Rubicon Genomics (Cat. No. R40012).

Techniques: Sequencing, Control, Modification

Alignment statistics.

Journal: PLoS ONE

Article Title: Exome Sequencing from Nanogram Amounts of Starting DNA: Comparing Three Approaches

doi: 10.1371/journal.pone.0101154

Figure Lengend Snippet: Alignment statistics.

Article Snippet: One library was prepared starting from 10 ng of sheared original DNA using ThruPLEX Fragmented DNA Prep kit (ThruPLEX-FD) from Rubicon Genomics (Cat. No. R40012).

Techniques:

Coverage statistics for the target region.

Journal: PLoS ONE

Article Title: Exome Sequencing from Nanogram Amounts of Starting DNA: Comparing Three Approaches

doi: 10.1371/journal.pone.0101154

Figure Lengend Snippet: Coverage statistics for the target region.

Article Snippet: One library was prepared starting from 10 ng of sheared original DNA using ThruPLEX Fragmented DNA Prep kit (ThruPLEX-FD) from Rubicon Genomics (Cat. No. R40012).

Techniques:

Pearson correlation coefficient with coverage profile of Standard ES strategy and average deviation from Standard ES coverage profile.

Journal: PLoS ONE

Article Title: Exome Sequencing from Nanogram Amounts of Starting DNA: Comparing Three Approaches

doi: 10.1371/journal.pone.0101154

Figure Lengend Snippet: Pearson correlation coefficient with coverage profile of Standard ES strategy and average deviation from Standard ES coverage profile.

Article Snippet: One library was prepared starting from 10 ng of sheared original DNA using ThruPLEX Fragmented DNA Prep kit (ThruPLEX-FD) from Rubicon Genomics (Cat. No. R40012).

Techniques:

Only variation with minimum depth of coverage of 20x and minimum quality of 13 were taken into account in all four strategies. The names of the samples are abbreviated: Standard ES = St; ThruPLEX-FD ES = Tp; REPLI-g ES = Rg; GenomePlex ES = Gp. The lower left tile presents the overall statistics, where “Total” indicates the number of all unique SNVs found in the region of interest, i.e. the union of SNV sets found by each strategy.

Journal: PLoS ONE

Article Title: Exome Sequencing from Nanogram Amounts of Starting DNA: Comparing Three Approaches

doi: 10.1371/journal.pone.0101154

Figure Lengend Snippet: Only variation with minimum depth of coverage of 20x and minimum quality of 13 were taken into account in all four strategies. The names of the samples are abbreviated: Standard ES = St; ThruPLEX-FD ES = Tp; REPLI-g ES = Rg; GenomePlex ES = Gp. The lower left tile presents the overall statistics, where “Total” indicates the number of all unique SNVs found in the region of interest, i.e. the union of SNV sets found by each strategy.

Article Snippet: One library was prepared starting from 10 ng of sheared original DNA using ThruPLEX Fragmented DNA Prep kit (ThruPLEX-FD) from Rubicon Genomics (Cat. No. R40012).

Techniques:

Comparison of SNVs found in regions with coverage > = 20 in both Standard ES and one of three tested strategies.

Journal: PLoS ONE

Article Title: Exome Sequencing from Nanogram Amounts of Starting DNA: Comparing Three Approaches

doi: 10.1371/journal.pone.0101154

Figure Lengend Snippet: Comparison of SNVs found in regions with coverage > = 20 in both Standard ES and one of three tested strategies.

Article Snippet: One library was prepared starting from 10 ng of sheared original DNA using ThruPLEX Fragmented DNA Prep kit (ThruPLEX-FD) from Rubicon Genomics (Cat. No. R40012).

Techniques: Comparison