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next-generation sequencing libraries  (Nextera AS)

 
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    Nextera AS next-generation sequencing libraries
    Next Generation Sequencing Libraries, supplied by Nextera AS, 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+library/next+generation+sequencing+libraries/pm30059786-357-2-6
    Average 90 stars, based on 1 article reviews
    next-generation sequencing libraries - by Bioz Stars, 2026-11
    90/100 stars

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    Related Articles

    Next-Generation Sequencing:

    Article Title: Cas12a/Cpf1 knock-in mice enable efficient multiplexed immune cell engineering
    Article Snippet: .. Nextera library preparation followed by Next Generation Sequencing was used to quantify the gene editing efficiency on molecular level. .. For all crRNAs targeting surface proteins in CD4 and CD8 T cells, higher indel percentages were observed compared to vector controls ( ). crCD4-1 generated the highest (66%) indels for the CD4 T cells ( , ).

    Article Title: Characterization of chromatin accessibility with a transposome hypersensitive sites sequencing (THS-seq) assay.
    Article Snippet: .. Caruccio N. Preparation of next-generation sequencing libraries using Nextera technology: simultaneous DNA fragmentation and adaptor tagging by in vitro transposition. ..

    Article Title: Striking antibody evasion manifested by the Omicron variant of SARS-CoV-2.
    Article Snippet: .. To verify the sequences of variants, next-generation sequencing libraries were prepared according to a low-volume Nextera sequencing protocol43 and sequenced on the Illumina Miseq platform (single-end mode with 50 bp R1). ..

    Article Title: In vivo CRISPR screening in CD8 T cells with AAV-Sleeping Beauty hybrid vectors identifies membrane targets for improving immunotherapy for glioblastoma.
    Article Snippet: .. DNA level analyses by surveyor assay and Nextera next generation sequencing demonstrated that PDIA3 knockout was highly efficient (86%) (Fig. 5b–d). ..

    Article Title: Multi-omic elucidation of aromatic catabolism in adaptively evolved Rhodococcus opacus.
    Article Snippet: .. Preparation of next-generation sequencing libraries using Nextera technology: simultaneous DNA fragmentation and adaptor tagging by in vitro transposition. ..

    In Vitro:

    Article Title: Characterization of chromatin accessibility with a transposome hypersensitive sites sequencing (THS-seq) assay.
    Article Snippet: .. Caruccio N. Preparation of next-generation sequencing libraries using Nextera technology: simultaneous DNA fragmentation and adaptor tagging by in vitro transposition. ..

    Article Title: Multi-omic elucidation of aromatic catabolism in adaptively evolved Rhodococcus opacus.
    Article Snippet: .. Preparation of next-generation sequencing libraries using Nextera technology: simultaneous DNA fragmentation and adaptor tagging by in vitro transposition. ..

    other:

    Article Title: Antifungal Triazole Posaconazole Targets an Early Stage of the Parechovirus A3 Life Cycle
    Article Snippet: Viruses from Vero-P passages 0 through 14 were sequenced using a Nextera XT next-generation sequencing (NGS) library kit and a 300-cycle (2 150-bp paired-end) MiSeq reagent kit, v2 (Illumina, San Diego, CA), as described previously (46).

    Article Title: Antifungal Triazole Posaconazole Targets an Early Stage of the Parechovirus A3 Life Cycle
    Article Snippet: Viruses from Vero-P passages 0 through 14 were sequenced using a Nextera XT next-generation sequencing (NGS) library kit and a 300-cycle (2× 150-bp paired-end) MiSeq reagent kit, v2 (Illumina, San Diego, CA), as described previously ( 46 ).

    Article Title: Whole genome sequencing-based drug resistance predictions of multidrug-resistant Mycobacterium tuberculosis isolates from Tanzania
    Article Snippet: Libraries for next generation sequencing (NGS) were prepared from gDNA using a modified Nextera protocol.

    Sequencing:

    Article Title: Striking antibody evasion manifested by the Omicron variant of SARS-CoV-2.
    Article Snippet: .. To verify the sequences of variants, next-generation sequencing libraries were prepared according to a low-volume Nextera sequencing protocol43 and sequenced on the Illumina Miseq platform (single-end mode with 50 bp R1). ..

    Knock-Out:

    Article Title: In vivo CRISPR screening in CD8 T cells with AAV-Sleeping Beauty hybrid vectors identifies membrane targets for improving immunotherapy for glioblastoma.
    Article Snippet: .. DNA level analyses by surveyor assay and Nextera next generation sequencing demonstrated that PDIA3 knockout was highly efficient (86%) (Fig. 5b–d). ..



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    Image Search Results


    Infection with E. aedis does not alter bacterial load in the abdomens of A. aegypti . The y ‐axis displays log10‐transformed ∆ X 0,16S values, which were obtained from analysis of quantitative PCR data, and represent the starting amount of 16S bacterial DNA in each sample normalized to the amount of RpS7 reference mosquito DNA. ∆ X 0,16S values serve as a proxy for measurement of bacterial load. The p value indicates the result of a mixed linear model testing the effect of E. aedis infection on log10‐transformed ∆ X 0,16S values.

    Journal: Environmental Microbiology

    Article Title: The Adult Aedes aegypti Bacterial Microbiota is Robust to Infection with the Obligate Microsporidian Parasite Edhazardia aedis

    doi: 10.1111/1462-2920.70437

    Figure Lengend Snippet: Infection with E. aedis does not alter bacterial load in the abdomens of A. aegypti . The y ‐axis displays log10‐transformed ∆ X 0,16S values, which were obtained from analysis of quantitative PCR data, and represent the starting amount of 16S bacterial DNA in each sample normalized to the amount of RpS7 reference mosquito DNA. ∆ X 0,16S values serve as a proxy for measurement of bacterial load. The p value indicates the result of a mixed linear model testing the effect of E. aedis infection on log10‐transformed ∆ X 0,16S values.

    Article Snippet: Amplicons were submitted to NC State Genomic Sciences Laboratory for subsequent library preparation following the Illumina 16S Metagenomic Sequencing Library Preparation guide ( 16S Metagenomic Sequencing Library Preparation: Preparing 16S Ribosomal RNA Gene Amplicons for the Illumina MiSeq System ).

    Techniques: Infection, Transformation Assay, Analysis, Real-time Polymerase Chain Reaction