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next-generation sequencing (ngs) custom targeted gene panel  (Illumina Inc)


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    Illumina Inc next-generation sequencing (ngs) custom targeted gene panel
    Next Generation Sequencing (Ngs) Custom Targeted Gene Panel, supplied by Illumina Inc, 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/custom+target+gene+sequencing+panel/next+generation+sequencing/pm40304077-61-10-24
    Average 90 stars, based on 1 article reviews
    next-generation sequencing (ngs) custom targeted gene panel - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Sequencing:

    Article Title: Oral cancer driver gene mutations in oral potentially malignant disorders: clinical significance and diagnostic implications.
    Article Snippet: .. Thus, we developed a custom target gene sequencing panel (AmpliSeq for Illumina Customs DNA Panel) capable of detecting full-length mutations in TP53, NOTCH1, CDKN2A, FBXW7, as well as mutations in HRAS, PIK3CA, and BRAF. ..

    Article Title: Oral cancer driver gene mutations in oral potentially malignant disorders: clinical significance and diagnostic implications
    Article Snippet: .. Thus, we developed a custom target gene sequencing panel (AmpliSeq for Illumina Customs DNA Panel) capable of detecting full-length mutations in TP53, NOTCH1, CDKN2A, FBXW7 , as well as mutations in HRAS, PIK3CA , and BRAF. ..



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    Fig.1 Flow diagram of the study design for NGS analysis. NGS, next-generation sequencing; OPMDs, oral potentially malignant disor- ders

    Journal: Discover oncology

    Article Title: Oral cancer driver gene mutations in oral potentially malignant disorders: clinical significance and diagnostic implications.

    doi: 10.1007/s12672-025-01923-7

    Figure Lengend Snippet: Fig.1 Flow diagram of the study design for NGS analysis. NGS, next-generation sequencing; OPMDs, oral potentially malignant disor- ders

    Article Snippet: Thus, we developed a custom target gene sequencing panel (AmpliSeq for Illumina Customs DNA Panel) capable of detecting full-length mutations in TP53, NOTCH1, CDKN2A, FBXW7, as well as mutations in HRAS, PIK3CA, and BRAF.

    Techniques: Next-Generation Sequencing

    Fig. 5 OLP case with ODGM. a–d Case with ODGM (case 15). a At the initial presentation, we observed non-removable white patches with mottled appearance and surrounding redness, leading to a clinical diagnosis of OLP. b A biopsy confirmed the histopathological diagnosis of OLP. c Eleven months after the initial presentation, a thickened white patch was observed on the posterior buccal mucosa. d A second biopsy led to a histopathological diagnosis of OED. e, f OLP case without ODGMs (Case 24). e Oral cavity image. f H&E staining. g Timeline of clinical course for case 15. ODGM, oral cancer driver gene mutation; OED, oral epithelial dysplasia; OLP, oral lichen planus; NGS, next- generation sequencing

    Journal: Discover oncology

    Article Title: Oral cancer driver gene mutations in oral potentially malignant disorders: clinical significance and diagnostic implications.

    doi: 10.1007/s12672-025-01923-7

    Figure Lengend Snippet: Fig. 5 OLP case with ODGM. a–d Case with ODGM (case 15). a At the initial presentation, we observed non-removable white patches with mottled appearance and surrounding redness, leading to a clinical diagnosis of OLP. b A biopsy confirmed the histopathological diagnosis of OLP. c Eleven months after the initial presentation, a thickened white patch was observed on the posterior buccal mucosa. d A second biopsy led to a histopathological diagnosis of OED. e, f OLP case without ODGMs (Case 24). e Oral cavity image. f H&E staining. g Timeline of clinical course for case 15. ODGM, oral cancer driver gene mutation; OED, oral epithelial dysplasia; OLP, oral lichen planus; NGS, next- generation sequencing

    Article Snippet: Thus, we developed a custom target gene sequencing panel (AmpliSeq for Illumina Customs DNA Panel) capable of detecting full-length mutations in TP53, NOTCH1, CDKN2A, FBXW7, as well as mutations in HRAS, PIK3CA, and BRAF.

    Techniques: Biomarker Discovery, Staining, Mutagenesis, Next-Generation Sequencing