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genome sequencing wgs data  (Genomics England)

 
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    Structured Review

    Genomics England genome sequencing wgs data
    Summary of clinical correlations adjusted for sex, age of sampling, and stage. A, ChCC ( n = 61) and ( B ) pRCC ( n = 103). CN, copy number; MB, megabase; SNV, single-nucleotide variant; TCRA, T-cell receptor-α; <t>WGII,</t> <t>whole-genome</t> instability index;ll *, P < 0.05.
    Genome Sequencing Wgs Data, supplied by Genomics England, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/genome+sequence+data/genome+sequencing+whole/pmc13136883-12-9-34
    Average 86 stars, based on 1 article reviews
    genome sequencing wgs data - by Bioz Stars, 2026-10
    86/100 stars

    Images

    1) Product Images from "Contrasting Features of Papillary and Chromophobe Renal Cell Carcinoma Revealed by Whole-Genome Sequencing"

    Article Title: Contrasting Features of Papillary and Chromophobe Renal Cell Carcinoma Revealed by Whole-Genome Sequencing

    Journal: Molecular Cancer Research

    doi: 10.1158/1541-7786.MCR-25-0616

    Summary of clinical correlations adjusted for sex, age of sampling, and stage. A, ChCC ( n = 61) and ( B ) pRCC ( n = 103). CN, copy number; MB, megabase; SNV, single-nucleotide variant; TCRA, T-cell receptor-α; WGII, whole-genome instability index;ll *, P < 0.05.
    Figure Legend Snippet: Summary of clinical correlations adjusted for sex, age of sampling, and stage. A, ChCC ( n = 61) and ( B ) pRCC ( n = 103). CN, copy number; MB, megabase; SNV, single-nucleotide variant; TCRA, T-cell receptor-α; WGII, whole-genome instability index;ll *, P < 0.05.

    Techniques Used: Sampling, Variant Assay

    Related Articles

    Sequencing:

    Article Title: Contrasting Features of Papillary and Chromophobe Renal Cell Carcinoma Revealed by Whole-Genome Sequencing
    Article Snippet: .. To address this shortcoming, we report the analysis of whole-genome sequencing (WGS) data generated on tumor–normal (T/N) pairs from 164 patients recruited from NHS Genomic Medicine Centres (GMC) across England, as part of the Genomics England 100,000 Genomes Project (100kGP, RRID: SCR_010502; refs , ). ..

    Article Title: Contrasting Features of Papillary and Chromophobe Renal Cell Carcinoma Revealed by Whole-Genome Sequencing
    Article Snippet: .. We analyzed whole-genome sequencing data on 164 tumor–normal pairs from the Genomics England 100,000 Genomes Project, providing a comprehensive, high-resolution map of copy number alterations, structural variation, and key global genomic features, including mutational signatures, intratumor heterogeneity, and analysis of extrachromosomal DNA formation. ..

    Article Title: Abstracts of the 18 th UK Neuromuscular Translational Research Conference 15 th and 16 th April 2025
    Article Snippet: .. Aims: Leveraging the Genomics England (GEL) Research Environment with extensive whole-genome sequencing (WGS) data, we aim to (1) identify DMPK repeat expansions in GEL data, classifying them into cohorts, (2) compare repeat length distributions across ancestries, and (3) establish a genotype-phenotype dataset linking individuals to phenotypes using Human Phenotype Ontology (HPO) terms. ..

    Article Title: Genetic variants in Rps4x cause intellectual disability with dysmorphic features, microcephaly, and autism.
    Article Snippet: .. Affected individuals and family members underwent whole genome sequencing as part of the 100KGP, as previously described (The National Genomic Research Library v5.1, Genomics England. https://doi.org/10.6084/m9.figshare.4530893.v7). ..

    Article Title: Pipeline Pruning: Exscientia Cuts Programs to Sharpen Precision Oncology Focus
    Article Snippet: GENEDGE Genetic Engineering & Biotechnology News: Edge Vol.. 5, No. 1, December 22, 2023 Copyright © GEN Publishing pp.. 889–897 DOI: 10.1089/genedge.5.1.170 Topics Artificial Intelligence

    Article Title: Combined multi-omics and multi-spectral profiling of plasma extracellular vesicles reveals liquid biopsy biomarkers for glioma diagnosis
    Article Snippet: .. • Additionally, for the training cohort, the raw microRNA sequencing proteomics data have been uploaded to the Genomics England Research Environment as required for data protection purposes. .. Research on the de-identified patient data from Genomics England used can be carried out in the Genomics England Research Environment subject to a collaborative agreement that adheres to patient-led governance.

    Whole Complete genome sequencing:

    Article Title: Contrasting Features of Papillary and Chromophobe Renal Cell Carcinoma Revealed by Whole-Genome Sequencing
    Article Snippet: .. To address this shortcoming, we report the analysis of whole-genome sequencing (WGS) data generated on tumor–normal (T/N) pairs from 164 patients recruited from NHS Genomic Medicine Centres (GMC) across England, as part of the Genomics England 100,000 Genomes Project (100kGP, RRID: SCR_010502; refs , ). ..

    Article Title: Abstracts of the 18 th UK Neuromuscular Translational Research Conference 15 th and 16 th April 2025
    Article Snippet: .. Aims: Leveraging the Genomics England (GEL) Research Environment with extensive whole-genome sequencing (WGS) data, we aim to (1) identify DMPK repeat expansions in GEL data, classifying them into cohorts, (2) compare repeat length distributions across ancestries, and (3) establish a genotype-phenotype dataset linking individuals to phenotypes using Human Phenotype Ontology (HPO) terms. ..

    Generated:

    Article Title: Contrasting Features of Papillary and Chromophobe Renal Cell Carcinoma Revealed by Whole-Genome Sequencing
    Article Snippet: .. To address this shortcoming, we report the analysis of whole-genome sequencing (WGS) data generated on tumor–normal (T/N) pairs from 164 patients recruited from NHS Genomic Medicine Centres (GMC) across England, as part of the Genomics England 100,000 Genomes Project (100kGP, RRID: SCR_010502; refs , ). ..



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    Genomics England whole genome sequencing data
    Summary of clinical correlations adjusted for sex, age of sampling, and stage. A, ChCC ( n = 61) and ( B ) pRCC ( n = 103). CN, copy number; MB, megabase; SNV, single-nucleotide variant; TCRA, T-cell receptor-α; <t>WGII,</t> <t>whole-genome</t> instability index;ll *, P < 0.05.
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    genome sequencing wgs data  (Genomics England)
    86
    Genomics England genome sequencing wgs data
    Summary of clinical correlations adjusted for sex, age of sampling, and stage. A, ChCC ( n = 61) and ( B ) pRCC ( n = 103). CN, copy number; MB, megabase; SNV, single-nucleotide variant; TCRA, T-cell receptor-α; <t>WGII,</t> <t>whole-genome</t> instability index;ll *, P < 0.05.
    Genome Sequencing Wgs Data, supplied by Genomics England, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/genome+sequence+data/genome+sequencing+whole/pmc13136883-12-9-34
    Average 86 stars, based on 1 article reviews
    genome sequencing wgs data - by Bioz Stars, 2026-10
    86/100 stars
    		  Buy from Supplier

    Image Search Results


    Summary of clinical correlations adjusted for sex, age of sampling, and stage. A, ChCC ( n = 61) and ( B ) pRCC ( n = 103). CN, copy number; MB, megabase; SNV, single-nucleotide variant; TCRA, T-cell receptor-α; WGII, whole-genome instability index;ll *, P < 0.05.

    Journal: Molecular Cancer Research

    Article Title: Contrasting Features of Papillary and Chromophobe Renal Cell Carcinoma Revealed by Whole-Genome Sequencing

    doi: 10.1158/1541-7786.MCR-25-0616

    Figure Lengend Snippet: Summary of clinical correlations adjusted for sex, age of sampling, and stage. A, ChCC ( n = 61) and ( B ) pRCC ( n = 103). CN, copy number; MB, megabase; SNV, single-nucleotide variant; TCRA, T-cell receptor-α; WGII, whole-genome instability index;ll *, P < 0.05.

    Article Snippet: We analyzed whole-genome sequencing data on 164 tumor–normal pairs from the Genomics England 100,000 Genomes Project, providing a comprehensive, high-resolution map of copy number alterations, structural variation, and key global genomic features, including mutational signatures, intratumor heterogeneity, and analysis of extrachromosomal DNA formation.

    Techniques: Sampling, Variant Assay

    Summary of clinical correlations adjusted for sex, age of sampling, and stage. A, ChCC ( n = 61) and ( B ) pRCC ( n = 103). CN, copy number; MB, megabase; SNV, single-nucleotide variant; TCRA, T-cell receptor-α; WGII, whole-genome instability index;ll *, P < 0.05.

    Journal: Molecular Cancer Research

    Article Title: Contrasting Features of Papillary and Chromophobe Renal Cell Carcinoma Revealed by Whole-Genome Sequencing

    doi: 10.1158/1541-7786.MCR-25-0616

    Figure Lengend Snippet: Summary of clinical correlations adjusted for sex, age of sampling, and stage. A, ChCC ( n = 61) and ( B ) pRCC ( n = 103). CN, copy number; MB, megabase; SNV, single-nucleotide variant; TCRA, T-cell receptor-α; WGII, whole-genome instability index;ll *, P < 0.05.

    Article Snippet: To address this shortcoming, we report the analysis of whole-genome sequencing (WGS) data generated on tumor–normal (T/N) pairs from 164 patients recruited from NHS Genomic Medicine Centres (GMC) across England, as part of the Genomics England 100,000 Genomes Project (100kGP, RRID: SCR_010502; refs , ).

    Techniques: Sampling, Variant Assay