sequencing flowcell Search Results


nanopore flongle flowcell sequencing library  (Oxford Nanopore)
90
Oxford Nanopore nanopore flongle flowcell sequencing library
The detection method for COVID-19 combined LAMP with <t>nanopore</t> <t>Flongle</t>
Nanopore Flongle Flowcell Sequencing Library, supplied by Oxford Nanopore, 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/product/sequencing+flowcell/nanopore+flongle+flowcell+sequencing+library/bio_rxiv__2020__06__03__131474-80-1-23
Average 90 stars, based on 1 article reviews
nanopore flongle flowcell sequencing library - by Bioz Stars, 2026-09
90/100 stars
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flowcells for nanopore sequencing  (Oxford Nanopore)
90
Oxford Nanopore flowcells for nanopore sequencing
A) Structural variant genotyping sensitivity using ONT reads. Genotypes were inferred for a set of 2,435 SVs using both Oxford Nanopore and Platinum Genomes (Illumina) alignments. Using reads from a random sample of X <t>flowcells,</t> sensitivity was calculated as the proportion of ONT-derived genotypes that were concordant with Illumina-derived genotypes. Error bars represent the standard deviation of sensitivity measurements from three randomly sampled sets of flowcells. B) Confusion matrix for genotype calling evaluation. Each cell contains the number of 1000 Genome sites for a particular (nanopolish, platinum) genotype combination.
Flowcells For Nanopore Sequencing, supplied by Oxford Nanopore, 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/product/sequencing+flowcell/flowcells+for+nanopore+sequencing/bio_rxiv__128835-333-18-38
Average 90 stars, based on 1 article reviews
flowcells for nanopore sequencing - by Bioz Stars, 2026-09
90/100 stars
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minion portable dna sequencer r9.4 flowcells  (Oxford Nanopore)
90
Oxford Nanopore minion portable dna sequencer r9.4 flowcells
A) Structural variant genotyping sensitivity using ONT reads. Genotypes were inferred for a set of 2,435 SVs using both Oxford Nanopore and Platinum Genomes (Illumina) alignments. Using reads from a random sample of X <t>flowcells,</t> sensitivity was calculated as the proportion of ONT-derived genotypes that were concordant with Illumina-derived genotypes. Error bars represent the standard deviation of sensitivity measurements from three randomly sampled sets of flowcells. B) Confusion matrix for genotype calling evaluation. Each cell contains the number of 1000 Genome sites for a particular (nanopolish, platinum) genotype combination.
Minion Portable Dna Sequencer R9.4 Flowcells, supplied by Oxford Nanopore, 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/product/sequencing+flowcell/minion+portable+dna+sequencer+r9+4+flowcells/pmc05838836__gix136_giga___d___17___00310_revision_1-192-14-18
Average 90 stars, based on 1 article reviews
minion portable dna sequencer r9.4 flowcells - by Bioz Stars, 2026-09
90/100 stars
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sequencing flowcell flongle  (Oxford Nanopore)
90
Oxford Nanopore sequencing flowcell flongle
A) Structural variant genotyping sensitivity using ONT reads. Genotypes were inferred for a set of 2,435 SVs using both Oxford Nanopore and Platinum Genomes (Illumina) alignments. Using reads from a random sample of X <t>flowcells,</t> sensitivity was calculated as the proportion of ONT-derived genotypes that were concordant with Illumina-derived genotypes. Error bars represent the standard deviation of sensitivity measurements from three randomly sampled sets of flowcells. B) Confusion matrix for genotype calling evaluation. Each cell contains the number of 1000 Genome sites for a particular (nanopolish, platinum) genotype combination.
Sequencing Flowcell Flongle, supplied by Oxford Nanopore, 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/product/sequencing+flowcell/sequencing+flowcell+flongle/pmc11438440-97-11-1
Average 90 stars, based on 1 article reviews
sequencing flowcell flongle - by Bioz Stars, 2026-09
90/100 stars
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minion r9 flowcell sequencing  (Oxford Nanopore)
90
Oxford Nanopore minion r9 flowcell sequencing
A) Structural variant genotyping sensitivity using ONT reads. Genotypes were inferred for a set of 2,435 SVs using both Oxford Nanopore and Platinum Genomes (Illumina) alignments. Using reads from a random sample of X <t>flowcells,</t> sensitivity was calculated as the proportion of ONT-derived genotypes that were concordant with Illumina-derived genotypes. Error bars represent the standard deviation of sensitivity measurements from three randomly sampled sets of flowcells. B) Confusion matrix for genotype calling evaluation. Each cell contains the number of 1000 Genome sites for a particular (nanopolish, platinum) genotype combination.
Minion R9 Flowcell Sequencing, supplied by Oxford Nanopore, 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/product/sequencing+flowcell/minion+r9+flowcell+sequencing/pmc09247103-308-28-26
Average 90 stars, based on 1 article reviews
minion r9 flowcell sequencing - by Bioz Stars, 2026-09
90/100 stars
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nanopore minion r9 flowcell sequencing  (Oxford Nanopore)
90
Oxford Nanopore nanopore minion r9 flowcell sequencing
A) Structural variant genotyping sensitivity using ONT reads. Genotypes were inferred for a set of 2,435 SVs using both Oxford Nanopore and Platinum Genomes (Illumina) alignments. Using reads from a random sample of X <t>flowcells,</t> sensitivity was calculated as the proportion of ONT-derived genotypes that were concordant with Illumina-derived genotypes. Error bars represent the standard deviation of sensitivity measurements from three randomly sampled sets of flowcells. B) Confusion matrix for genotype calling evaluation. Each cell contains the number of 1000 Genome sites for a particular (nanopolish, platinum) genotype combination.
Nanopore Minion R9 Flowcell Sequencing, supplied by Oxford Nanopore, 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/product/sequencing+flowcell/nanopore+minion+r9+flowcell+sequencing/bio_rxiv__2021__12__14__472731-50-3-1
Average 90 stars, based on 1 article reviews
nanopore minion r9 flowcell sequencing - by Bioz Stars, 2026-09
90/100 stars
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gridion sequencer oxford nanopore release 18.02 flowcell r9.4.a revd  (Oxford Nanopore)
90
Oxford Nanopore gridion sequencer oxford nanopore release 18.02 flowcell r9.4.a revd
A) Structural variant genotyping sensitivity using ONT reads. Genotypes were inferred for a set of 2,435 SVs using both Oxford Nanopore and Platinum Genomes (Illumina) alignments. Using reads from a random sample of X <t>flowcells,</t> sensitivity was calculated as the proportion of ONT-derived genotypes that were concordant with Illumina-derived genotypes. Error bars represent the standard deviation of sensitivity measurements from three randomly sampled sets of flowcells. B) Confusion matrix for genotype calling evaluation. Each cell contains the number of 1000 Genome sites for a particular (nanopolish, platinum) genotype combination.
Gridion Sequencer Oxford Nanopore Release 18.02 Flowcell R9.4.A Revd, supplied by Oxford Nanopore, 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/product/sequencing+flowcell/gridion+sequencer+oxford+nanopore+release+18+02+flowcell+r9+4+a+revd/bio_rxiv__647750-195-24-17
Average 90 stars, based on 1 article reviews
gridion sequencer oxford nanopore release 18.02 flowcell r9.4.a revd - by Bioz Stars, 2026-09
90/100 stars
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r10 flongle sequencing flowcells  (Oxford Nanopore)
90
Oxford Nanopore r10 flongle sequencing flowcells
A) Structural variant genotyping sensitivity using ONT reads. Genotypes were inferred for a set of 2,435 SVs using both Oxford Nanopore and Platinum Genomes (Illumina) alignments. Using reads from a random sample of X <t>flowcells,</t> sensitivity was calculated as the proportion of ONT-derived genotypes that were concordant with Illumina-derived genotypes. Error bars represent the standard deviation of sensitivity measurements from three randomly sampled sets of flowcells. B) Confusion matrix for genotype calling evaluation. Each cell contains the number of 1000 Genome sites for a particular (nanopolish, platinum) genotype combination.
R10 Flongle Sequencing Flowcells, supplied by Oxford Nanopore, 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/product/sequencing+flowcell/r10+flongle+sequencing+flowcells/bio_rxiv__2023__09__05__556370-112-18-23
Average 90 stars, based on 1 article reviews
r10 flongle sequencing flowcells - by Bioz Stars, 2026-09
90/100 stars
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Image Search Results


The detection method for COVID-19 combined LAMP with nanopore Flongle

Journal: bioRxiv

Article Title: Rapid detection of SARS-CoV-2 and other respiratory viruses by using LAMP method with Nanopore Flongle workflow

doi: 10.1101/2020.06.03.131474

Figure Lengend Snippet: The detection method for COVID-19 combined LAMP with nanopore Flongle

Article Snippet: A nanopore Flongle flowcell sequencing library was prepared using 200 ng of DNA amplification product (amplification 30 minutes) as input to SQK-RBK004 kit (Oxford Nanopore Technology, UK).

Techniques:

Nanopore Flongle different running time SARS-CoV-2 detection (A) Flongle different running time sequenced and detected reads numbers to reference; (B) Flongle different running time aligned reads assign to different target gene number

Journal: bioRxiv

Article Title: Rapid detection of SARS-CoV-2 and other respiratory viruses by using LAMP method with Nanopore Flongle workflow

doi: 10.1101/2020.06.03.131474

Figure Lengend Snippet: Nanopore Flongle different running time SARS-CoV-2 detection (A) Flongle different running time sequenced and detected reads numbers to reference; (B) Flongle different running time aligned reads assign to different target gene number

Article Snippet: A nanopore Flongle flowcell sequencing library was prepared using 200 ng of DNA amplification product (amplification 30 minutes) as input to SQK-RBK004 kit (Oxford Nanopore Technology, UK).

Techniques:

Nanopore demultiplexed and detected reads number of each sample

Journal: bioRxiv

Article Title: Rapid detection of SARS-CoV-2 and other respiratory viruses by using LAMP method with Nanopore Flongle workflow

doi: 10.1101/2020.06.03.131474

Figure Lengend Snippet: Nanopore demultiplexed and detected reads number of each sample

Article Snippet: A nanopore Flongle flowcell sequencing library was prepared using 200 ng of DNA amplification product (amplification 30 minutes) as input to SQK-RBK004 kit (Oxford Nanopore Technology, UK).

Techniques:

A) Structural variant genotyping sensitivity using ONT reads. Genotypes were inferred for a set of 2,435 SVs using both Oxford Nanopore and Platinum Genomes (Illumina) alignments. Using reads from a random sample of X flowcells, sensitivity was calculated as the proportion of ONT-derived genotypes that were concordant with Illumina-derived genotypes. Error bars represent the standard deviation of sensitivity measurements from three randomly sampled sets of flowcells. B) Confusion matrix for genotype calling evaluation. Each cell contains the number of 1000 Genome sites for a particular (nanopolish, platinum) genotype combination.

Journal: bioRxiv

Article Title: Nanopore sequencing and assembly of a human genome with ultra-long reads

doi: 10.1101/128835

Figure Lengend Snippet: A) Structural variant genotyping sensitivity using ONT reads. Genotypes were inferred for a set of 2,435 SVs using both Oxford Nanopore and Platinum Genomes (Illumina) alignments. Using reads from a random sample of X flowcells, sensitivity was calculated as the proportion of ONT-derived genotypes that were concordant with Illumina-derived genotypes. Error bars represent the standard deviation of sensitivity measurements from three randomly sampled sets of flowcells. B) Confusion matrix for genotype calling evaluation. Each cell contains the number of 1000 Genome sites for a particular (nanopolish, platinum) genotype combination.

Article Snippet: ML, NL, JOG, JTS, JRT, and TPS were members of the MinION access program (MAP) and have received free-of-charge flowcells and kits for nanopore sequencing for this and other studies, and travel and accommodation expenses to speak at Oxford Nanopore Technologies conferences.

Techniques: Variant Assay, Derivative Assay, Standard Deviation