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sureselect clinical research exome v.2 kit  (Agilent technologies)


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    Structured Review

    Agilent technologies sureselect clinical research exome v.2 kit
    Sureselect Clinical Research Exome V.2 Kit, supplied by Agilent technologies, 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/sureselect+clinical+research+exome+kit/med_rxiv__2024__08__08__24311713-27-15-21
    Average 90 stars, based on 1 article reviews
    sureselect clinical research exome v.2 kit - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    other:

    Article Title: Aminopeptidase Expression in Multiple Myeloma Associates with Disease Progression and Sensitivity to Melflufen
    Article Snippet: The SeqCap ® EZ MedExome kit (Roche NimbleGen, Madison, WI), SureSelect Clinical Research Exome kit, or SureSelect Human All Exon V5 kit (Agilent Technologies, Santa Clara, CA) was used for exome capture.

    Article Title: RNA analysis of intronic variants in the LAMA2 gene detected by whole genome sequencing confirms a rare dual diagnosis of incontinentia pigmenti with limb‐girdle muscular dystrophy
    Article Snippet: The Agilent SureSelect Clinical Research Exome kit was used to target known coding sequences and splice junctions of known protein‐coding genes associated with disease using genomic DNA from the submitted sample(s).

    Article Title: The feasibility of using liquid biopsies as a complementary assay for copy number aberration profiling in routinely collected paediatric cancer patient samples.
    Article Snippet: Library construction for WES on tumour tissue samples (n Z 4) was performed with the SureSelect Clinical Research Exome kit (Agilent Technologies, US), SeqCap EZ Exome kit 3.0 (Roche, Switzerland), or the SeqCap EZ MedExome kit (Roche, Switzerland) according to the manufacturer’s instructions.

    Sequencing:

    Article Title: Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delay.
    Article Snippet: .. ES was performed for the proband in family A and as a trio in families B, C, and D. Technical details have been previously described for family C.5 In brief, sample library was prepared using Nextera Extension Exome RapidCapture kit (Illumina, San Diego, CA, USA) for family A; Agilent SureSelect Clinical Research Exome kit mixed with an enhanced capture protocol for family B; Ion Proton AmpliSeq library using Exome Primer Pools and AmpliSeq HiFi mix (Thermo Fisher, Carlsbad, CA, USA) for family C; and xGEN (IDT, Coralville, IA, USA) with subsequent TruSeq DNA Library Prep for Enrichment (IDT Exome, Illumina) for family D. Exome libraries were run on Illumina HiSeq2500 (Illumina) for families A and B, Ion Proton instrument (Thermo Fisher) for family C, and NextSeq (Illumina) for family D. Sequencing reads were aligned to the reference genome GRCh37/hg19 and variants were filtered according to established pipelines (Supplemental Material). ..

    Article Title: Comparison of Biomarker Assays for EGFR : Implications for Precision Medicine in Patients with Glioblastoma
    Article Snippet: Tumor genomic DNA was extracted using the QIAGEN AllPrep Kit (QIAGEN Sciences, Germantown, MD, USA). .. Whole exome sequencing libraries were prepared using the SureSelect Clinical Research Exome kit (Agilent, Cedar Creek, TX, USA). .. Sequencing was performed with an Illumina HiSeq 2500 (2 × 100 base pairs) (Illumina, Hayward, CA, USA).

    Article Title: Epithelial recurrent erosion dystrophy (ERED) from the splice site altering COL17A1 variant c.3156C>T in families of Finnish-Swedish ancestry.
    Article Snippet: .. Briefly, sequencing libraries were prepared with NimbleGen Exome v2 kit (Roche, San Diego, USA) and SureSelect Clinical Research Exome kit (Agilent Technologies, Santa Clara, USA), and sequenced on HiSeq 2500 system (Illumina). ..

    Article Title: A recurrent de novo splice site variant involving DNM1 exon 10a causes developmental and epileptic encephalopathy through a dominant-negative mechanism
    Article Snippet: .. Whole-exome sequencing was performed in seven individuals by GeneDx with the IDT xGen Exome Research Panel v1.0 (Integrated DNA Technologies); in one individual by the Hospital for Sick Children (Toronto, Canada) using the Agilent SureSelect Focused Exome Kit (Agilent); in one individual at Hôpital de la Pitié Salpêtrière (Paris, France) using the SeqCap EZ MedExome Library kit (NimbleGen, Roche Sequencing); and in one individual by CHOP using the Agilent SureSelect Clinical Research Exome Kit (Agilent). ..

    Whole-Exome Sequencing:

    Article Title: Integrated Analysis of the Pancreas and Islets Reveals Unexpected Findings in Human Male With Type 1 Diabetes
    Article Snippet: .. Whole-exome sequencing was performed using the Agilent SureSelect Clinical Research Exome Kit (Agilent Technologies) on Illumina NextSeq technology with 150-bp paired end reads and mean depth of coverage over 150×. ..



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