Trusight Hereditary Cancer Panel

Listing Websites about Trusight Hereditary Cancer Panel

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TruSight Hereditary Cancer Panel Used with Nextera Flex

(Just Now) TruSight Hereditary Cancer Panel was created as a modular panel that uses Illumina DNA Prep with Enrichment for library preparation. Indexes are available for up to 384 samples to allow for flexible batch sizes and scalability across all Illumina benchtop sequencers (iSeq 100, MiSeq, MiniSeq, and NextSeq).

https://www.illumina.com/products/by-type/clinical-research-products/trusight-cancer-hereditary.html

Category:  Cancer Show Health

TruSight Hereditary Cancer Panel Used with Nextera Flex

(9 days ago) The TruSight Hereditary Cancer Panel workflow requires the TruSight Hereditary Cancer oligos, Nextera Flex Library Prep and Enrichment Reagents, IDT for Illumina Nextera DNA UD indexes, and sequencing reagents. 价格. TruSight Hereditary Cancer – Enrichment Oligos Only (8 Enrichment Reactions) 20029551. 联系我们.

http://supportassets.illumina.com/products/by-type/clinical-research-products/trusight-cancer-hereditary.html

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TruSight Cancer Sequence cancer predisposition-related …

(9 days ago) TruSight Cancer Sample Datasets. 6 human reference samples were prepared using the TruSight Cancer sequencing panel. These libraries were sequenced on the MiniSeq System using a high output kit at a 2 x 100 bp read length configuration with dual indexing. The total yield was 5.2 Gb with 95.8% of bases at or above Q30.

https://www.illumina.com/products/by-type/clinical-research-products/trusight-cancer.html

Category:  Cancer Show Health

TruSight Sequencing Panels - Illumina, Inc.

(4 days ago) TruSight Cancer. Targeting genes previously linked to a predisposition towards cancer. TruSight Tumor 15. Focused panel assesses common somatic variants in solid tumors. TruSight Cardio. Focusing on identifying inherited cardiac conditions. TruSight Inherited Disease. Focusing on severe, recessive pediatric onset diseases.

https://www.illumina.com/products/trusight-panels.html

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TruSight Cancer Sequencing Panel - Illumina, Inc.

(4 days ago) TruSight Cancer and TruSight Rapid Capture enable researchers to analyze precious samples, while retaining sufficient material for future analyses. Content Design Strategy The TruSight Cancer Sequencing Panel was developed in collaboration with Professor Nazneen Rahman and team at The Institute of Cancer Research (ICR), London.

https://www.illumina.com/Documents/products/datasheets/datasheet_trusight_cancer.pdf

Category:  Cancer Show Health

TruSight Hereditary Cancer Panel - Illumina GeneTiCA

(6 days ago) TruSight Hereditary Cancer Panel - Illumina. TruSight Hereditary Cancer panel bol navrhnutý spoločnosťou Illumina pre určenie genetického rizika výskytu rôznych druhov nádorových ochorení využitím NGS technológie.Tento kit umožňuje detegovať až 113 génov a 125 SNP súvisiacich s predispozíciou k nádorovému ochoreniu vďaka 10 341 oligo próbam, ktoré pokrývajú všetky

https://www.genetica.sk/trusight-hereditary-cancer-panel

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TruSight Cancer Sequencing Panel - Illumina, Inc.

(9 days ago) associated with cancer. The sequencing panel is compatible with TruSight Rapid Capture kits, providing a single, integrated sample preparation and enrichment workflow that can be completed in just 1.5 days (Figure 1). Delivering excellent data quality from low sample input (50 ng), TruSight Cancer and TruSight Rapid Capture enable

https://assets.illumina.com/content/dam/illumina-marketing/apac/china/documents/datasheet_trusight_cancer.pdf

Category:  Cancer Show Health

TruSight Oncology 500 and TruSight Oncology 500 …

(7 days ago) community to design content for the TruSight Oncology 500 and TruSight Oncology 500 High-Throughput panels. The resulting panels provide comprehensive coverage of biomarkers commonly mutated in numerous cancer types (Figure 2), including 523 genes for single nucleotide variants (SNVs), insertions/deletions (indels), copy number

https://www.ndsu.edu/pubweb/~mcclean/plsc411/twig/trusight-oncology-500-and-ht-data-sheet-1170-2018-010.pdf

Category:  Cancer Show Health

Hereditary Neuroendocrine Tumor Disorders Risk …

(9 days ago) Hereditary cancer syndrome is a genetic predisposition to develop certain types of cancers, often at an enriched using hybrid capture Illumina TruSight Cancer Sequencing Panel. Single base pair (point) mutations, small insertions/deletions (1-25 bp), complex insertions and

https://www.henryford.com/-/media/files/henry-ford/hcp/pathology/hereditary-neuroendocrine-tumor-risk-panel.pdf?la=en&hash=4106915D1AA8354712E9CBC6A1795290

Category:  Cancer Show Health

TruSight One Sequencing Panels Manifest File Download

(6 days ago) TruSight One Expanded Gene List v3.0. ZIP (< 1 MB) May 9, 2018. TruSight One Expanded File for UCSC Browser v2.0 (BED Format) ZIP (1 MB) Nov 30, 2017. TruSight One Sequencing Panel Manifest (TXT Format) ZIP (< 1 MB) Mar 14, 2014.

https://support.illumina.com/downloads/trusight_one_sequencing_panel_product_file.html

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Hereditary Cancer Genetic Testing Panel CancerNext by

(2 days ago) CancerNext is a comprehensive 36-gene panel that identifies inherited risks for at least 8 types of cancers. CancerNext is a comprehensive 36-gene panel that identifies inherited risks for at least 8 types of cancers. CancerNext is a comprehensive 36-gene panel that identifies inherited risks for at least 8 types of cancers.

https://www.ambrygen.com/providers/genetic-testing/1/oncology/cancernext

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Cancer Germline Mutation Detection Hereditary cancer

(8 days ago) TruSight Hereditary Cancer Panel. Expert-defined research panel targeting 113 genes associated with genetic cancer risk predisposition. AmpliSeq for Illumina BRCA Panel. Targeted research panel investigating somatic and germline variants in BRCA1 and BRCA2.

https://supportassets.illumina.com/content/illumina-marketing/en/areas-of-interest/cancer/clinical-cancer-research/germline-mutations.html

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Hereditary Cancer - Fulgent Genetics - Leader in Next

(1 days ago) Comprehensive. Fulgent Comprehensive Cancer Panels cover 127 genes associated with potential risk for hereditary cancer syndromes. These panels include well-established cancer-related genes as well as candidate genes with newly discovered association …

https://www.fulgentgenetics.com/products/oncology/hereditarycancer.html

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Hereditary Melanoma Panel - Expanded (8 genes)

(4 days ago) Hereditary cancer syndrome is a genetic predisposition to develop certain types of cancers, often at an enriched using hybrid capture Illumina TruSight Cancer Sequencing Panel. Single base pair (point) mutations, small insertions/deletions (1-25 bp), complex insertions and

https://www.henryford.com/-/media/files/henry-ford/hcp/pathology/11hereditary-melanoma-panel-expanded-8-genes-olena-200505.pdf?la=en&hash=EE046F3FC121FB36DAA72DCA4FE8B339

Category:  Cancer Show Health

TruSight RNA Pan-Cancer Panel Reference Guide

(8 days ago) This guide contains everything a first-time user needs, including an overview of the TruSight RNA Pan-Cancer Panel protocol, tips and techniques, protocol steps, kit contents, and user-supplied consumables.

https://emea.support.illumina.com/downloads/trusight-rna-pan-cancer-panel-reference-guide-1000000001632.html

Category:  Cancer Show Health

Illumina Launches TruSight Oncology 500 to Power

(8 days ago) Illumina Launches TruSight Oncology 500 to Power Comprehensive, Accurate, Pan-Cancer Tumor Profiling. SAN DIEGO-- (BUSINESS WIRE)--Oct. 30, 2018-- Illumina, Inc. (NASDAQ: ILMN) today announces the launch of TruSight TM Oncology 500 (TSO 500), a comprehensive pan-cancer assay designed to identify known and emerging tumor biomarkers.

https://emea.illumina.com/company/news-center/press-releases/2018/2374252.html

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Understanding the Polygenicity of Cancer

(2 days ago) The beauty of the TruSight Hereditary Cancer Panel is that it provides a less expensive way of sequencing than standard captures. It’s amazing that the technology can combine thousands of primer pairs and somehow get them all to work together. It has exciting potential and it’s great that we’ll be able to scale it from a MiSeq System up

https://emea.illumina.com/science/customer-stories/icommunity-customer-interviews-case-studies/weitzel-coh-interview-ts-hereditary-cancer.html

Category:  Cancer Show Health

Illumina DNA Prep with Enrichment Fast, flexible

(5 days ago) TruSight Hereditary Cancer – Enrichment Oligos Only (8 Enrichment Reactions) 20029551. Price . TruSight One – Enrichment Oligos only (6 Enrichment Reactions) 20029227. AmpliSeq for Illumina Comprehensive Cancer Panel . Targeted panel investigating the exonic regions of 409 genes with known associations to cancer.

https://emea.illumina.com/products/by-type/sequencing-kits/library-prep-kits/nextera-flex-enrichment.html

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TruSight Myeloid Sequencing Panel: Targets hematological

(1 days ago) The TruSight Myeloid Sequencing Panel uses expert-defined content and proven next-generation sequencing (NGS) technology to identify somatic variants in myeloid malignancies. The panel content was designed by a consortium of recognized experts in blood cancer disorders and targets genes frequently mutated in:

https://emea.illumina.com/products/by-type/clinical-research-products/trusight-myeloid.html

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TruSight RNA Pan-Cancer Panel Product Files

(Just Now) TruSight RNA Pan-Cancer Target Regions Files. Target region files for the TruSight RNA Pan-Cancer panel. View Options. TruSight RNA Pan-Cancer Target Regions File (GTF Format) < 1 MB. Feb 3, 2016. TruSight RNA Pan-Cancer Target Regions File (BED Format) < 1 MB. Feb 3, 2016.

https://support.illumina.com/sequencing/sequencing_kits/trusight-rna-pan-cancer-panel/downloads.html

Category:  Cancer Show Health

TruSight RNA Pan-Cancer Panel Study cancer gene fusions

(9 days ago) TruSight RNA Pan-Cancer Sample Datasets. Note that access to this data requires a login. Register for BaseSpace Sequence Hub. MiSeq Data. 10 ng of human reference RNA (UHR), human reference brain RNA (Brain), cell line RNA (MCF7), and 20 ng of breast tumor FFPE RNA (BT) were prepared using the TruSight RNA Pan-Cancer Panel and sequenced on the MiSeq System.

https://sapac.illumina.com/products/by-type/clinical-research-products/trusight-rna-pan-cancer.html

Category:  Cancer Show Health

TruSight RNA Fusion Panel Documentation

(Just Now) TruSight RNA Fusion Panel Checklist. This checklist is a condensed form of the TruSight RNA Fusion Panel protocol. It is easy to print and carry with you in the lab. Download. < 1 MB. Oct 27, 2016. TruSight RNA Fusion Panel Consumables & Equipment. Consumables …

https://support.illumina.com/sequencing/sequencing_kits/trusight-rna-fusion-panel/documentation.html

Category:  Cancer Show Health

TruSight Oncology 500 ctDNA Assay blood plasma for pan

(3 days ago) TruSight Oncology ctDNA is a pan-cancer next-generation sequencing (NGS) assay that enables in-house comprehensive genomic profiling (CGP) from blood plasma. The broad panel is designed with similar DNA content as its tissue counterparts (TruSight Oncology 500 and TruSight Oncology 500 High-Throughput), including key immuno-oncology (IO

https://sapac.illumina.com/products/by-type/clinical-research-products/trusight-oncology-500-ctdna.html

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TruSight Oncology 500 Portfolio

(8 days ago) The TruSight Oncology 500 portfolio enables in-house, pan-cancer comprehensive genomic profiling (CGP) for solid tumors from either blood or tissue biopsy samples. All three assays in the portfolio, shown below, are designed to identify relevant biomarkers in guidelines and trials, including the immuno-oncology markers TMB and MSI.

https://emea.illumina.com/products/by-brand/trusight-oncology-500.html?scid=2020-271PPC2482&catt=Online%20Advertising_Google%20Adwords-biomarker

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TruSight RNA Pan-Cancer Panel FAQs - Illumina, Inc.

(5 days ago) TruSight RNA Pan-Cancer is a large gene panel covering 1385 cancer-related genes. TruSeq Targeted RNA Expression typically provides smaller panels and fusion detection is more difficult. Additionally, TruSight RNA Pan-Cancer has discovery power for fusion detection because only one gene fusion partner is required.

https://emea.support.illumina.com/sequencing/sequencing_kits/trusight-rna-pan-cancer-panel/questions.html

Category:  Cancer Show Health

TruSight Oncology Reagents to detect cancer variants

(3 days ago) The comprehensive nature of this methodology provides laboratories with a deep view into the genetics of cancer. Accurate Results from Low-Quality Samples 1 TruSight RNA Fusion Panel. Provides comprehensive gene fusion detection in formalin-fixed, paraffin-embedded (FFPE) and other cancer research samples.

https://sapac.illumina.com/products/by-type/clinical-research-products/trusight-oncology.html

Category:  Cancer Show Health

Evaluation of CNV detection tools for NGS panel data in

(Just Now) hybridization-based target capture NGS panels designed for hereditary cancer diagnostics: TruSight Cancer Panel (Illu-mina, San Diego, CA, USA) and I2HCP [16]. TruSight Cancer Panel v2 (100

https://www.researchgate.net/publication/342326211_Evaluation_of_CNV_detection_tools_for_NGS_panel_data_in_genetic_diagnostics/fulltext/5ef31c51a6fdcc158d260fd7/Evaluation-of-CNV-detection-tools-for-NGS-panel-data-in-genetic-diagnostics.pdf

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TruSight Oncology UMI Reagents Unique molecular

(7 days ago) TruSight Oncology UMI Reagents do not contain any enrichment probes. If you wish to use the TruSight Tumor 170 DNA probe set, purchase the TruSight Tumor 170 Content Set separately. Cancer Panels for Targeted Sequencing. our goal is to apply innovative technologies to the analysis of genetic variation and function, making studies

https://sapac.illumina.com/products/by-type/clinical-research-products/trusight-oncology-umi.html

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GeneTiCA - imagine the NEXT

(4 days ago) 16. 04. 2021 - 10x Genomics: Training Sessions - from sample to data with Single Cell Platform. 15. 04. 2021 - 10x Genomics: Spatial Discovery. 12. 04. 2021 - The New York Times Magazine Highlights the Power of Sequencing.

https://www.genetica.sk/

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Full Comprehensive Cancer Panel Fulgent Genetics

(6 days ago) The Full Comprehensive Cancer Panel examines 127 genes associated with hereditary cancer. This panel includes both well-established genes that increase a person’s risk for cancer, but also includes candidate genes that may have only been recently discovered or for which additional research is needed. This panel maximizes the chances of

https://www.fulgentgenetics.com/comprehensivecancer-full

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TruSight RNA Fusion Panel Support - Questions & Answers

(6 days ago) TruSight RNA Fusion is a large gene panel covering 507 cancer-related genes. TruSeq Targeted RNA Expression typically provides smaller panels and fusion detection is more difficult. Additionally, TruSight RNA Fusion has discovery power for fusion detection because only one gene fusion partner is required.

https://support.illumina.com/sequencing/sequencing_kits/trusight-rna-fusion-panel/questions.html

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TruSight Oncology 500 High-Throughput For use with

(Just Now) TruSight Oncology 500 High-Throughput TruSight Oncology 500 TruSight Oncology 500 ctDNA; Cancer Type: Pan-Cancer: Pan-Cancer: Pan-Cancer: Content Specifications: Targeted selection of DNA from 523 genes of interest, and RNA from 55 genes, for a total of 1.94Mb panel size. • Guideline Coverage: Broad coverage of key guidelines for multiple

https://sapac.illumina.com/products/by-type/clinical-research-products/trusight-oncology-500-ht.html

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TruSight Cancer Content Set Product Files

(4 days ago) TruSight Cancer Content Set Manifest File A. TXT (< 1 MB) Feb 5, 2013. TruSight Cancer Content Set BED File A. BED (< 1 MB) Feb 5, 2013.

https://supportetp.tst-web.illumina.com/downloads/trusight_cancer_product_files.html

Category:  Cancer Show Health

TruSight Oncology 500 Documentation - Illumina, Inc.

(1 days ago) TruSight Oncology 500 Local App Documentation. Instructions for installing and using the TruSight Oncology 500 Local App. View Options. TruSight Oncology 500 v2.2 Local App User Guide (1000000137777 v01) < 1 MB. Oct 12, 2021. TruSight Oncology 500 v2.2 Local App Release Notes (1000000142775 v00) < 1 MB. Nov 13, 2020.

https://emea.support.illumina.com/sequencing/sequencing_kits/trusight-oncology-500/documentation.html

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TruSight Myeloid Sequencing Panel FAQs

(9 days ago) TruSight Myeloid amplicons are 225–275 bp in length. What genes are covered in the TruSight Myeloid assay? The TruSight Myeloid Sequencing Panel targets 54 genes (either full coding sequence or targeted exons) that are frequently mutated in myeloid malignancies. Refer to the TruSight Myeloid Sequencing Panel Data Sheet for a full list of genes.

https://emea.support.illumina.com/sequencing/sequencing_kits/trusight-myeloid-sequencing-panel/questions.html

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Benchmarking of Whole Exome Sequencing and Ad Hoc Designed

(1 days ago) Hereditary cancer accounts for about 3% of all cancers (reviewed by Rahman) 1,2 and is caused by inherited or de novo germline mutations in high-penetrance predisposition cancer genes

https://www.nature.com/articles/srep37984

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TruSight One Sequencing Panel Reference Guide

(1 days ago) Instructions for using the TruSight One Sequencing Panel Library Prep Kit to prepare up to 36 indexed paired-end libraries, followed by enrichment using the TruSight One Content Set.

https://support.illumina.com/downloads/trusight_one_capture_sample_prep_guide_15046431.html

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Abstract P2-09-18: Exploration of the - Cancer Research

(7 days ago) All of them were prescreened by direct sequencing and MLPA analysis, and tested negative for pathogenic mutations in BRCA1 and BRCA2 genes. Next generation target resequencing using a panel of 94 cancer related genes (Illumina TruSight cancer panel) was performed to explore the hereditary component beyond BRCA1/2 genes in these patients.

https://cancerres.aacrjournals.org/content/76/4_Supplement/P2-09-18

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Benchmarking of Whole Exome Sequencing and Ad Hoc Designed

(1 days ago) The performance of two panels is compared to exome sequencing. Twenty-four patients were selected: ten with identified mutations (control set) and fourteen suspicious of hereditary cancer but with no mutation (discovery set). TruSight Cancer (94 genes) and a custom panel (122 genes) were assessed alongside exome sequencing.

https://pubmed.ncbi.nlm.nih.gov/28050010/

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