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ribo zero human mouse rat set b illumina 20020612 qubit dna high sensitivity kit thermo fisher scientific q32851 sureselect xt hs2 dna kits  (Illumina Inc)


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    Structured Review

    Illumina Inc ribo zero human mouse rat set b illumina 20020612 qubit dna high sensitivity kit thermo fisher scientific q32851 sureselect xt hs2 dna kits
    Ribo Zero Human Mouse Rat Set B Illumina 20020612 Qubit Dna High Sensitivity Kit Thermo Fisher Scientific Q32851 Sureselect Xt Hs2 Dna Kits, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 96/100, based on 241 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/sureselect+xt+libraries/TruSeq+Stranded+Total+RNA+Library+Prep+Globin/pm39948187-251-133-137
    Average 96 stars, based on 241 article reviews
    ribo zero human mouse rat set b illumina 20020612 qubit dna high sensitivity kit thermo fisher scientific q32851 sureselect xt hs2 dna kits - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    other:

    Article Title: Mapping effector genes at lupus GWAS loci using promoter Capture-C in follicular helper T cells.
    Article Snippet: SureSelect XT libraries were then paired-end sequenced on 8 lanes of Illumina Hiseq 4000 platform (100 bp read length).

    Article Title: Implicating type 2 diabetes effector genes in relevant metabolic cellular models using promoter-focused Capture-C
    Article Snippet: SureSelect XT libraries were then paired-end sequenced either the Illumina HiSeq 4000 or on Illumina NovaSeq 6000 platform (51 bp read length).

    Functional Assay:

    Article Title: Integrative genomics identifies lncRNA regulatory networks across 1,044 pediatric leukemias and extra-cranial solid tumors
    Article Snippet: .. SureSelect XT libraries were then paired-end sequenced on Illumina NovaSeq 6000 platform (51bp read length) at the Center for Spatial and Functional Genomics at CHOP. ..

    Article Title: Variant-to-gene-mapping followed by cross-species genetic screening identifies GPI-anchor biosynthesis as novel regulator of sleep
    Article Snippet: .. SureSelect XT libraries were then paired-end sequenced on Illumina NovaSeq 6000 platform (51bp read length) at the Center for Spatial and Functional Genomics at CHOP. ..

    Article Title: Variant-to-gene mapping followed by cross-species genetic screening identifies GPI-anchor biosynthesis as a regulator of sleep
    Article Snippet: .. SureSelect XT libraries were then paired-end–sequenced on Illumina NovaSeq 6000 platform (51-bp read length) at the Center for Spatial and Functional Genomics at CHOP. ..

    Article Title: Cis-regulatory architecture of human ESC-derived hypothalamic neuron differentiation aids in variant-to-gene mapping of relevant complex traits
    Article Snippet: .. SureSelect XT libraries were then paired-end sequenced on Illumina NovaSeq 6000 platform (51 bp read length) at the Center for Spatial and Functional Genomics at CHOP. ..

    Article Title: Cis-regulatory architecture of human ESC-derived hypothalamic neuron differentiation aids in variant-to-gene mapping of relevant complex traits
    Article Snippet: .. SureSelect XT libraries were then paired-end sequenced on Illumina NovaSeq 6000 platform (51bp read length) at the Center for Spatial and Functional Genomics at CHOP. ..



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    Sampling process. Timeline of biopsy, blood, and stool specimen collection. Tumor biopsies were taken before any treatment was initiated. Blood and stool samples were collected before neoadjuvant chemoradiotherapy (CRT) and optionally in the interval between CRT completion and curative surgery (up to eight weeks after CRT completion). Biopsy samples were analyzed using the <t>SureSelect</t> TM XT HS-focused <t>exome</t> panel comprising 4800 genes and regions, whereas blood and stool samples were investigated using the AVENIO TM ctDNA surveillance panel covering 197 genes and regions. FFPE: formalin-fixed, paraffin-embedded; cfDNA: cell-free DNA, ctDNA: cell-free tumor DNA, CRT: chemoradiotherapy. Figure created with Biorender.com.
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    Image Search Results


    Sampling process. Timeline of biopsy, blood, and stool specimen collection. Tumor biopsies were taken before any treatment was initiated. Blood and stool samples were collected before neoadjuvant chemoradiotherapy (CRT) and optionally in the interval between CRT completion and curative surgery (up to eight weeks after CRT completion). Biopsy samples were analyzed using the SureSelect TM XT HS-focused exome panel comprising 4800 genes and regions, whereas blood and stool samples were investigated using the AVENIO TM ctDNA surveillance panel covering 197 genes and regions. FFPE: formalin-fixed, paraffin-embedded; cfDNA: cell-free DNA, ctDNA: cell-free tumor DNA, CRT: chemoradiotherapy. Figure created with Biorender.com.

    Journal: Technology in Cancer Research & Treatment

    Article Title: Combined DNA Analysis from Stool and Blood Samples Improves Tumor Tracking and Assessment of Clonal Heterogeneity in Localized Rectal Cancer Patients

    doi: 10.1177/15330338241252706

    Figure Lengend Snippet: Sampling process. Timeline of biopsy, blood, and stool specimen collection. Tumor biopsies were taken before any treatment was initiated. Blood and stool samples were collected before neoadjuvant chemoradiotherapy (CRT) and optionally in the interval between CRT completion and curative surgery (up to eight weeks after CRT completion). Biopsy samples were analyzed using the SureSelect TM XT HS-focused exome panel comprising 4800 genes and regions, whereas blood and stool samples were investigated using the AVENIO TM ctDNA surveillance panel covering 197 genes and regions. FFPE: formalin-fixed, paraffin-embedded; cfDNA: cell-free DNA, ctDNA: cell-free tumor DNA, CRT: chemoradiotherapy. Figure created with Biorender.com.

    Article Snippet: Because the AVENIO TM Tumor Tissue targeted kit was not available at the time, which covers the same genetic regions as the AVENIO TM ctDNA Library Prep Kit used for plasma and stool samples, the SureSelect TM XT HS Target Enrichment Kit in combination with the SureSelect TM XT HS Focused Exome capture library (Agilent, Santa Clara, USA, cat. no. G9702A; 5190-7787) was used for tissue and resection mutation analysis.

    Techniques: Sampling, Formalin-fixed Paraffin-Embedded

    Sequencing Metrics of Individual Sequencing Approaches.

    Journal: Technology in Cancer Research & Treatment

    Article Title: Combined DNA Analysis from Stool and Blood Samples Improves Tumor Tracking and Assessment of Clonal Heterogeneity in Localized Rectal Cancer Patients

    doi: 10.1177/15330338241252706

    Figure Lengend Snippet: Sequencing Metrics of Individual Sequencing Approaches.

    Article Snippet: Because the AVENIO TM Tumor Tissue targeted kit was not available at the time, which covers the same genetic regions as the AVENIO TM ctDNA Library Prep Kit used for plasma and stool samples, the SureSelect TM XT HS Target Enrichment Kit in combination with the SureSelect TM XT HS Focused Exome capture library (Agilent, Santa Clara, USA, cat. no. G9702A; 5190-7787) was used for tissue and resection mutation analysis.

    Techniques: Sequencing, Mutagenesis

    Mutational allelic frequencies, numbers, and direct comparisons of identified mutations in different specimens. (A) Allelic frequencies (AF) of mutations identified in different sample specimens. (B) Comparison of AF of detected mutations in paired plasma and stool samples derived from the same patients. (C) Number of identified mutations per patient within different sample specimens. (D) Number of shared and non-shared mutations in the same patient across different specimen comparisons. (E) Number of intersecting mutations in different specimens across all patients (n = 9) from whom all three specimens were analyzed. Only mutations that are covered by both the SureSelect TM (biopsy) and AVENIO TM (plasma and stool) panel are depicted. Numbers above lines in graphs (A–C) represent p-values.

    Journal: Technology in Cancer Research & Treatment

    Article Title: Combined DNA Analysis from Stool and Blood Samples Improves Tumor Tracking and Assessment of Clonal Heterogeneity in Localized Rectal Cancer Patients

    doi: 10.1177/15330338241252706

    Figure Lengend Snippet: Mutational allelic frequencies, numbers, and direct comparisons of identified mutations in different specimens. (A) Allelic frequencies (AF) of mutations identified in different sample specimens. (B) Comparison of AF of detected mutations in paired plasma and stool samples derived from the same patients. (C) Number of identified mutations per patient within different sample specimens. (D) Number of shared and non-shared mutations in the same patient across different specimen comparisons. (E) Number of intersecting mutations in different specimens across all patients (n = 9) from whom all three specimens were analyzed. Only mutations that are covered by both the SureSelect TM (biopsy) and AVENIO TM (plasma and stool) panel are depicted. Numbers above lines in graphs (A–C) represent p-values.

    Article Snippet: Because the AVENIO TM Tumor Tissue targeted kit was not available at the time, which covers the same genetic regions as the AVENIO TM ctDNA Library Prep Kit used for plasma and stool samples, the SureSelect TM XT HS Target Enrichment Kit in combination with the SureSelect TM XT HS Focused Exome capture library (Agilent, Santa Clara, USA, cat. no. G9702A; 5190-7787) was used for tissue and resection mutation analysis.

    Techniques: Comparison, Derivative Assay

    Comparison of identified mutations across different sample specimens in individual patients. (A) Mutational lesions detected in either tumor biopsy, plasma, or stool samples in individual patients. (B) Mutational analysis in patients from whom plasma and stool samples were available before (plasma/stool) and after (plasma_T2/stool_T2) therapeutic intervention. (C) Comparison of variants detected in tumor biopsies and liquid biopsies (plasma) in patients from whom stool mutational analysis was not available. (D) Comparison of mutations in different sample specimens of patient 1462 whose plasma and stool mutation profile is compared to a resection of the whole tumor (resection). Timeline of the course of disease, sample collection, and therapeutic interventions of Pat 1462 are depicted. Genes marked with X in tissue samples are not covered by the SureSelect TM sequencing panel used for biopsy specimen analysis. Gene names represent individual mutational positions within a certain gene. Grey gene names represent synonymous mutations. Color code represents allelic frequency. CRT: chemoradiotherapy; cfDNA: cell-free DNA.

    Journal: Technology in Cancer Research & Treatment

    Article Title: Combined DNA Analysis from Stool and Blood Samples Improves Tumor Tracking and Assessment of Clonal Heterogeneity in Localized Rectal Cancer Patients

    doi: 10.1177/15330338241252706

    Figure Lengend Snippet: Comparison of identified mutations across different sample specimens in individual patients. (A) Mutational lesions detected in either tumor biopsy, plasma, or stool samples in individual patients. (B) Mutational analysis in patients from whom plasma and stool samples were available before (plasma/stool) and after (plasma_T2/stool_T2) therapeutic intervention. (C) Comparison of variants detected in tumor biopsies and liquid biopsies (plasma) in patients from whom stool mutational analysis was not available. (D) Comparison of mutations in different sample specimens of patient 1462 whose plasma and stool mutation profile is compared to a resection of the whole tumor (resection). Timeline of the course of disease, sample collection, and therapeutic interventions of Pat 1462 are depicted. Genes marked with X in tissue samples are not covered by the SureSelect TM sequencing panel used for biopsy specimen analysis. Gene names represent individual mutational positions within a certain gene. Grey gene names represent synonymous mutations. Color code represents allelic frequency. CRT: chemoradiotherapy; cfDNA: cell-free DNA.

    Article Snippet: Because the AVENIO TM Tumor Tissue targeted kit was not available at the time, which covers the same genetic regions as the AVENIO TM ctDNA Library Prep Kit used for plasma and stool samples, the SureSelect TM XT HS Target Enrichment Kit in combination with the SureSelect TM XT HS Focused Exome capture library (Agilent, Santa Clara, USA, cat. no. G9702A; 5190-7787) was used for tissue and resection mutation analysis.

    Techniques: Comparison, Mutagenesis, Sequencing