fragment sizes Search Results


geobacpcr fragment size  (Federation of European Neuroscience Societies)
90
Federation of European Neuroscience Societies geobacpcr fragment size
Geobacpcr Fragment Size, supplied by Federation of European Neuroscience Societies, 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/fragment+sizes/geobacpcr+fragment+size/pm18031336-112-39-18
Average 90 stars, based on 1 article reviews
geobacpcr fragment size - by Bioz Stars, 2026-09
90/100 stars
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panel of 50 synthetic 12- mer peptides  (GenScript corporation)
90
GenScript corporation panel of 50 synthetic 12- mer peptides
Panel Of 50 Synthetic 12 Mer Peptides, supplied by GenScript corporation, 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/fragment+sizes/oligonucleotide+fragments+with+sizes+of+50++100++150++200++500++and+1+500+bp/pm36424884-41-26-42
Average 90 stars, based on 1 article reviews
panel of 50 synthetic 12- mer peptides - by Bioz Stars, 2026-09
90/100 stars
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custom bead purification protocol spri size selection protocol for >1.5-2 kb dna fragments  (Oxford Nanopore)
90
Oxford Nanopore custom bead purification protocol spri size selection protocol for >1.5-2 kb dna fragments
Each line plot represents the read size distribution from each mock community species estimated from <t>the</t> <t>Nanopore</t> metagenome data. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is in-house data generated from a ZymoBIOMICS Microbial Community <t>DNA</t> Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell. Some species have significantly more high molecular weight DNA over 5000 bp compared to some of the other species, which impacts the effective template availability in PCR for long amplicons. For the Loman lab data, the distinct gram+/- dependent trends fragment length is anticipated from their two step extraction protocol used on the mock community. The in-house generated data is generated from DNA standard prepared by the vendor, and here the taxa trend is not as pronounced, but the effect on the effective relative abundance is still dramatic . We can only speculate about the cause, but different extraction methods could be the reason. If all samples had been extracted with the same method, the result should be more similar fragment distributions as indicated by the Loman group data. The Nanopore library preparation and sequencing likely had an impact on the observed read fragment distributions, but the Loman group data indicates that extraction method probably is the most important factor.
Custom Bead Purification Protocol Spri Size Selection Protocol For >1.5 2 Kb Dna Fragments, 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/fragment+sizes/custom+bead+purification+protocol+spri+size+selection+protocol+for++1+5+2+kb+dna+fragments/bio_rxiv__645903-82-17-20
Average 90 stars, based on 1 article reviews
custom bead purification protocol spri size selection protocol for >1.5-2 kb dna fragments - by Bioz Stars, 2026-09
90/100 stars
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size-selected fragments from genomic dna  (Ecogenics GmbH)
90
Ecogenics GmbH size-selected fragments from genomic dna
Each line plot represents the read size distribution from each mock community species estimated from <t>the</t> <t>Nanopore</t> metagenome data. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is in-house data generated from a ZymoBIOMICS Microbial Community <t>DNA</t> Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell. Some species have significantly more high molecular weight DNA over 5000 bp compared to some of the other species, which impacts the effective template availability in PCR for long amplicons. For the Loman lab data, the distinct gram+/- dependent trends fragment length is anticipated from their two step extraction protocol used on the mock community. The in-house generated data is generated from DNA standard prepared by the vendor, and here the taxa trend is not as pronounced, but the effect on the effective relative abundance is still dramatic . We can only speculate about the cause, but different extraction methods could be the reason. If all samples had been extracted with the same method, the result should be more similar fragment distributions as indicated by the Loman group data. The Nanopore library preparation and sequencing likely had an impact on the observed read fragment distributions, but the Loman group data indicates that extraction method probably is the most important factor.
Size Selected Fragments From Genomic Dna, supplied by Ecogenics GmbH, 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/fragment+sizes/size+selected+fragments+from+genomic+dna/pmc04103121-66-5-11
Average 90 stars, based on 1 article reviews
size-selected fragments from genomic dna - by Bioz Stars, 2026-09
90/100 stars
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academic dna double-strand breaks and dna fragment size distributions  (Attix Pharmaceuticals)
90
Attix Pharmaceuticals academic dna double-strand breaks and dna fragment size distributions
Each line plot represents the read size distribution from each mock community species estimated from <t>the</t> <t>Nanopore</t> metagenome data. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is in-house data generated from a ZymoBIOMICS Microbial Community <t>DNA</t> Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell. Some species have significantly more high molecular weight DNA over 5000 bp compared to some of the other species, which impacts the effective template availability in PCR for long amplicons. For the Loman lab data, the distinct gram+/- dependent trends fragment length is anticipated from their two step extraction protocol used on the mock community. The in-house generated data is generated from DNA standard prepared by the vendor, and here the taxa trend is not as pronounced, but the effect on the effective relative abundance is still dramatic . We can only speculate about the cause, but different extraction methods could be the reason. If all samples had been extracted with the same method, the result should be more similar fragment distributions as indicated by the Loman group data. The Nanopore library preparation and sequencing likely had an impact on the observed read fragment distributions, but the Loman group data indicates that extraction method probably is the most important factor.
Academic Dna Double Strand Breaks And Dna Fragment Size Distributions, supplied by Attix Pharmaceuticals, 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/fragment+sizes/academic+dna+double+strand+breaks+and+dna+fragment+size+distributions/pm09712548-491-3-10
Average 90 stars, based on 1 article reviews
academic dna double-strand breaks and dna fragment size distributions - by Bioz Stars, 2026-09
90/100 stars
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fragment size distributions  (CH Instruments)
90
CH Instruments fragment size distributions
Each line plot represents the read size distribution from each mock community species estimated from <t>the</t> <t>Nanopore</t> metagenome data. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is in-house data generated from a ZymoBIOMICS Microbial Community <t>DNA</t> Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell. Some species have significantly more high molecular weight DNA over 5000 bp compared to some of the other species, which impacts the effective template availability in PCR for long amplicons. For the Loman lab data, the distinct gram+/- dependent trends fragment length is anticipated from their two step extraction protocol used on the mock community. The in-house generated data is generated from DNA standard prepared by the vendor, and here the taxa trend is not as pronounced, but the effect on the effective relative abundance is still dramatic . We can only speculate about the cause, but different extraction methods could be the reason. If all samples had been extracted with the same method, the result should be more similar fragment distributions as indicated by the Loman group data. The Nanopore library preparation and sequencing likely had an impact on the observed read fragment distributions, but the Loman group data indicates that extraction method probably is the most important factor.
Fragment Size Distributions, supplied by CH Instruments, 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/fragment+sizes/fragment+size+distributions/10__1007_slash_s00603___024___04079___y-308-0-21
Average 90 stars, based on 1 article reviews
fragment size distributions - by Bioz Stars, 2026-09
90/100 stars
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full-size human β 1 sgc cdna fragment af 020340  (Promega)
90
Promega full-size human β 1 sgc cdna fragment af 020340
Each line plot represents the read size distribution from each mock community species estimated from <t>the</t> <t>Nanopore</t> metagenome data. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is in-house data generated from a ZymoBIOMICS Microbial Community <t>DNA</t> Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell. Some species have significantly more high molecular weight DNA over 5000 bp compared to some of the other species, which impacts the effective template availability in PCR for long amplicons. For the Loman lab data, the distinct gram+/- dependent trends fragment length is anticipated from their two step extraction protocol used on the mock community. The in-house generated data is generated from DNA standard prepared by the vendor, and here the taxa trend is not as pronounced, but the effect on the effective relative abundance is still dramatic . We can only speculate about the cause, but different extraction methods could be the reason. If all samples had been extracted with the same method, the result should be more similar fragment distributions as indicated by the Loman group data. The Nanopore library preparation and sequencing likely had an impact on the observed read fragment distributions, but the Loman group data indicates that extraction method probably is the most important factor.
Full Size Human β 1 Sgc Cdna Fragment Af 020340, supplied by Promega, 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/fragment+sizes/full+size+human+%CE%B2+1+sgc+cdna+fragment+af+020340/pmc00208791-40-1-13
Average 90 stars, based on 1 article reviews
full-size human β 1 sgc cdna fragment af 020340 - by Bioz Stars, 2026-09
90/100 stars
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xhoi fragment size  (Promega)
90
Promega xhoi fragment size
Each line plot represents the read size distribution from each mock community species estimated from <t>the</t> <t>Nanopore</t> metagenome data. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is in-house data generated from a ZymoBIOMICS Microbial Community <t>DNA</t> Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell. Some species have significantly more high molecular weight DNA over 5000 bp compared to some of the other species, which impacts the effective template availability in PCR for long amplicons. For the Loman lab data, the distinct gram+/- dependent trends fragment length is anticipated from their two step extraction protocol used on the mock community. The in-house generated data is generated from DNA standard prepared by the vendor, and here the taxa trend is not as pronounced, but the effect on the effective relative abundance is still dramatic . We can only speculate about the cause, but different extraction methods could be the reason. If all samples had been extracted with the same method, the result should be more similar fragment distributions as indicated by the Loman group data. The Nanopore library preparation and sequencing likely had an impact on the observed read fragment distributions, but the Loman group data indicates that extraction method probably is the most important factor.
Xhoi Fragment Size, supplied by Promega, 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/fragment+sizes/xhoi+fragment+size/pmc02206644-146-8-11
Average 90 stars, based on 1 article reviews
xhoi fragment size - by Bioz Stars, 2026-09
90/100 stars
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smaller sized fragments of pollen  (Informa UK Limited)
90
Informa UK Limited smaller sized fragments of pollen
Each line plot represents the read size distribution from each mock community species estimated from <t>the</t> <t>Nanopore</t> metagenome data. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is in-house data generated from a ZymoBIOMICS Microbial Community <t>DNA</t> Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell. Some species have significantly more high molecular weight DNA over 5000 bp compared to some of the other species, which impacts the effective template availability in PCR for long amplicons. For the Loman lab data, the distinct gram+/- dependent trends fragment length is anticipated from their two step extraction protocol used on the mock community. The in-house generated data is generated from DNA standard prepared by the vendor, and here the taxa trend is not as pronounced, but the effect on the effective relative abundance is still dramatic . We can only speculate about the cause, but different extraction methods could be the reason. If all samples had been extracted with the same method, the result should be more similar fragment distributions as indicated by the Loman group data. The Nanopore library preparation and sequencing likely had an impact on the observed read fragment distributions, but the Loman group data indicates that extraction method probably is the most important factor.
Smaller Sized Fragments Of Pollen, supplied by Informa UK Limited, 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/fragment+sizes/smaller+sized+fragments+of+pollen/pm34607495-14-30-25
Average 90 stars, based on 1 article reviews
smaller sized fragments of pollen - by Bioz Stars, 2026-09
90/100 stars
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single-molecule sequencing of long-size dna fragments  (Oxford Nanopore)
90
Oxford Nanopore single-molecule sequencing of long-size dna fragments
Each line plot represents the read size distribution from each mock community species estimated from <t>the</t> <t>Nanopore</t> metagenome data. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is in-house data generated from a ZymoBIOMICS Microbial Community <t>DNA</t> Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell. Some species have significantly more high molecular weight DNA over 5000 bp compared to some of the other species, which impacts the effective template availability in PCR for long amplicons. For the Loman lab data, the distinct gram+/- dependent trends fragment length is anticipated from their two step extraction protocol used on the mock community. The in-house generated data is generated from DNA standard prepared by the vendor, and here the taxa trend is not as pronounced, but the effect on the effective relative abundance is still dramatic . We can only speculate about the cause, but different extraction methods could be the reason. If all samples had been extracted with the same method, the result should be more similar fragment distributions as indicated by the Loman group data. The Nanopore library preparation and sequencing likely had an impact on the observed read fragment distributions, but the Loman group data indicates that extraction method probably is the most important factor.
Single Molecule Sequencing Of Long Size Dna Fragments, 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/fragment+sizes/single+molecule+sequencing+of+long+size+dna+fragments/pm37365249-40-8-3
Average 90 stars, based on 1 article reviews
single-molecule sequencing of long-size dna fragments - by Bioz Stars, 2026-09
90/100 stars
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genscan (fragment sizing)  (Tech Dragon)
90
Tech Dragon genscan (fragment sizing)
Each line plot represents the read size distribution from each mock community species estimated from <t>the</t> <t>Nanopore</t> metagenome data. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is in-house data generated from a ZymoBIOMICS Microbial Community <t>DNA</t> Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell. Some species have significantly more high molecular weight DNA over 5000 bp compared to some of the other species, which impacts the effective template availability in PCR for long amplicons. For the Loman lab data, the distinct gram+/- dependent trends fragment length is anticipated from their two step extraction protocol used on the mock community. The in-house generated data is generated from DNA standard prepared by the vendor, and here the taxa trend is not as pronounced, but the effect on the effective relative abundance is still dramatic . We can only speculate about the cause, but different extraction methods could be the reason. If all samples had been extracted with the same method, the result should be more similar fragment distributions as indicated by the Loman group data. The Nanopore library preparation and sequencing likely had an impact on the observed read fragment distributions, but the Loman group data indicates that extraction method probably is the most important factor.
Genscan (Fragment Sizing), supplied by Tech Dragon, 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/fragment+sizes/genscan++fragment+sizing+/pmc03585910-201-17-13
Average 90 stars, based on 1 article reviews
genscan (fragment sizing) - by Bioz Stars, 2026-09
90/100 stars
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sonication to an average fragment size of 200–400 using bioruptor ucd-300-to  (DIAGENODE DIAGNOSTICS)
90
DIAGENODE DIAGNOSTICS sonication to an average fragment size of 200–400 using bioruptor ucd-300-to
Each line plot represents the read size distribution from each mock community species estimated from <t>the</t> <t>Nanopore</t> metagenome data. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is in-house data generated from a ZymoBIOMICS Microbial Community <t>DNA</t> Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell. Some species have significantly more high molecular weight DNA over 5000 bp compared to some of the other species, which impacts the effective template availability in PCR for long amplicons. For the Loman lab data, the distinct gram+/- dependent trends fragment length is anticipated from their two step extraction protocol used on the mock community. The in-house generated data is generated from DNA standard prepared by the vendor, and here the taxa trend is not as pronounced, but the effect on the effective relative abundance is still dramatic . We can only speculate about the cause, but different extraction methods could be the reason. If all samples had been extracted with the same method, the result should be more similar fragment distributions as indicated by the Loman group data. The Nanopore library preparation and sequencing likely had an impact on the observed read fragment distributions, but the Loman group data indicates that extraction method probably is the most important factor.
Sonication To An Average Fragment Size Of 200–400 Using Bioruptor Ucd 300 To, supplied by DIAGENODE DIAGNOSTICS, 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/fragment+sizes/sonication+to+an+average+fragment+size+of+200+400+using+bioruptor+ucd+300+to/pmc07452874-146-10-22
Average 90 stars, based on 1 article reviews
sonication to an average fragment size of 200–400 using bioruptor ucd-300-to - by Bioz Stars, 2026-09
90/100 stars
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Image Search Results


Each line plot represents the read size distribution from each mock community species estimated from the Nanopore metagenome data. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is in-house data generated from a ZymoBIOMICS Microbial Community DNA Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell. Some species have significantly more high molecular weight DNA over 5000 bp compared to some of the other species, which impacts the effective template availability in PCR for long amplicons. For the Loman lab data, the distinct gram+/- dependent trends fragment length is anticipated from their two step extraction protocol used on the mock community. The in-house generated data is generated from DNA standard prepared by the vendor, and here the taxa trend is not as pronounced, but the effect on the effective relative abundance is still dramatic . We can only speculate about the cause, but different extraction methods could be the reason. If all samples had been extracted with the same method, the result should be more similar fragment distributions as indicated by the Loman group data. The Nanopore library preparation and sequencing likely had an impact on the observed read fragment distributions, but the Loman group data indicates that extraction method probably is the most important factor.

Journal: bioRxiv

Article Title: Enabling high-accuracy long-read amplicon sequences using unique molecular identifiers with Nanopore or PacBio sequencing

doi: 10.1101/645903

Figure Lengend Snippet: Each line plot represents the read size distribution from each mock community species estimated from the Nanopore metagenome data. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is in-house data generated from a ZymoBIOMICS Microbial Community DNA Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell. Some species have significantly more high molecular weight DNA over 5000 bp compared to some of the other species, which impacts the effective template availability in PCR for long amplicons. For the Loman lab data, the distinct gram+/- dependent trends fragment length is anticipated from their two step extraction protocol used on the mock community. The in-house generated data is generated from DNA standard prepared by the vendor, and here the taxa trend is not as pronounced, but the effect on the effective relative abundance is still dramatic . We can only speculate about the cause, but different extraction methods could be the reason. If all samples had been extracted with the same method, the result should be more similar fragment distributions as indicated by the Loman group data. The Nanopore library preparation and sequencing likely had an impact on the observed read fragment distributions, but the Loman group data indicates that extraction method probably is the most important factor.

Article Snippet: The PCR product was purified using a custom bead purification protocol “SPRI size selection protocol for >1.5-2 kb DNA fragments” (Oxford Nanopore, England) based on: dx.doi.org/10.17504/protocols.io.idmca46.

Techniques: Generated, High Molecular Weight, Extraction, Sequencing

Read coverage profiles of the ZymoBIOMICS Microbial Community DNA Standard based on shotgun Nanopore sequencing data. Each grey point is the average coverage value of a 10 kbp region within the genome. Colored points represents the position of the individual intragenomic rRNA operons. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [product D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is our data generated from a ZymoBIOMICS Microbial Community DNA Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell.

Journal: bioRxiv

Article Title: Enabling high-accuracy long-read amplicon sequences using unique molecular identifiers with Nanopore or PacBio sequencing

doi: 10.1101/645903

Figure Lengend Snippet: Read coverage profiles of the ZymoBIOMICS Microbial Community DNA Standard based on shotgun Nanopore sequencing data. Each grey point is the average coverage value of a 10 kbp region within the genome. Colored points represents the position of the individual intragenomic rRNA operons. A) is data generated from a ZymoBIOMICS Microbial Community Standard (even) [product D6300, batch ZRC190633] by the Loman lab using the Nanopore GridION and a R9.4.1 flowcell. B) is our data generated from a ZymoBIOMICS Microbial Community DNA Standard (even) [product D6306, batch ZRC190811] using Nanopore MinION and a R10 flowcell.

Article Snippet: The PCR product was purified using a custom bead purification protocol “SPRI size selection protocol for >1.5-2 kb DNA fragments” (Oxford Nanopore, England) based on: dx.doi.org/10.17504/protocols.io.idmca46.

Techniques: Nanopore Sequencing, Generated