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trusight oncology 500 kit  (Illumina Inc)


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    Structured Review

    Illumina Inc trusight oncology 500 kit
    Trusight Oncology 500 Kit, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 95/100, based on 108 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/trusight/TruSight+Oncology+500+DNA%2FRNA+Kit/pm42791032-61-25-29
    Average 95 stars, based on 108 article reviews
    trusight oncology 500 kit - by Bioz Stars, 2026-10
    95/100 stars

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    Related Articles

    Sequencing:

    Article Title: Biallelic Variants in the DARS2 Gene as a Novel Cause of Axonal Charcot-Marie-Tooth Disease.
    Article Snippet: Berta Estévez-Arias, MSc ,1,2,3 Siiri Sarv, MSc ,4 Nathalie Bonello-Palot, PhD ,5,6 Laura Carrera-García, MD,1,7 Carlos Ortez, MD,1,7 Jesica Exp osito-Escudero, MD,1,7 Delia Yubero, PhD,8,9 Jordi Muchart, MD,10 Emilien Delmont, MD,11 Eve Õiglane-Shlik, MD, PhD,4,12 Teele Meren, MD,13 Sanna Puusepp, MD, PhD,14 Ülle Murumets, MD,13 Gajja S. Salomons, PhD,15 Bjarne Udd, MD, PhD,16,17,18 Liis Väli, MD, PhD,4,19 Lara Cantarero, PhD,2,8 Carsten G. Bönnemann, MD ,20 Andrés Nascimento, MD, PhD,1,7,8 Santiago Ram on-Maiques, PhD,8,21,22 Katrin Õunap, MD, PhD,4,13 Janet Hoenicka, PhD ,2,8‡ Daniel Natera-de Benito, MD, PhD ,1,7,8‡ and Francesc Palau, MD, PhD 2,8,23,24‡

    Article Title: Biallelic Variants in the DARS2 Gene as a Novel Cause of Axonal Charcot–Marie–Tooth Disease
    Article Snippet: .. Sequencing was performed with different panels: TruSight One Expanded (Illumina; 6713 genes) for individual A1, ClearSeq Inherited Disease (Agilent; 2742 genes) for B1, and TruSight One (Illumina; 4813 genes) for C1. .. Additionally, trio exome sequencing was performed for family C. Paired‐end sequencing was performed on Illumina NextSeq500 System (Illumina) or Ion Proton (Thermo Fisher Scientific) platforms.

    other:

    Article Title: AGITG MONARCC: A Randomized Phase 2 Study of Panitumumab Monotherapy and Panitumumab Plus 5-Fluorouracil as First-Line Therapy for Older Patients With RAS and BRAF Wild Type Metastatic Colorectal Cancer. A Study by the Australasian Gastro-Intestinal Trials Group (AGITG).
    Article Snippet: Lower intensity anti EGFR antibody containing regimens may be suitable for older persons with RAS and BRAF wild type metastatic colorectal cancer.. We found promising activity of 2 such regimens which are worthy of use in selected patients.. Background: Panitumumab (pan) plus chemotherapy is a preferred first-line therapy for unresectable RAS and BRAF wild type metastatic colorectal cancer (mCRC).

    Article Title: DICER1 in pediatric and adult cancer predisposition populations: prevalence, phenotypes and mosaics.
    Article Snippet: For the pediatric cohort, library preparation was performed using the TruSight One expanded Sequencing Panel (TSOex; Illumina, San Diego, CA, USA) from 2017 to July 2020 and the SureSelect Clinical Research Exome v2 (SSCRE; Agilent, Santa Clara, CA, USA) from August 2020 to January 2022, followed by paired-end sequencing in a NextSeq 500 System (Illumina, San Diego, CA, USA).

    Article Title: Sanger validation of WGS variants
    Article Snippet: Arteche-López et al. , Clinical Exome (1109 variants) , TruSight (Illumina), NextSeq (Illumina) , ranged from 20x to 361x, with a mean of 107.74x , FILTER = PASS, QUAL ≥ 100 DP ≥ 20 AF ≥ 0.2.

    Article Title: Long-Read Whole-Genome Sequencing as a Tool for Variant Detection in Inherited Retinal Dystrophies
    Article Snippet: To test the clinical applications of this technique in IRD cases, we selected a cohort of patients who had previously undergone clinical exome sequencing (CES) using either Clinical Exome Solution (Sophia Genetics, Boston, MA, USA) or TruSight One (Illumina, San Diego, CA, USA), and/or whole-exome sequencing (WES), as described in Perea-Romero et al. [ ].

    Article Title: Genomic insights into inherited bone marrow failure syndromes in a Korean population.
    Article Snippet: The TruSight One expanded sequencing panel (Illumina, Inc., San Diego, CA, USA) was selected for CES, covering 6704 genes and 86 000 exons associated with almost all known Mendelian genomic disorders.



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