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variant calling algorithm  (AstraZeneca ltd)

 
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    AstraZeneca ltd variant calling algorithm
    Variant Calling Algorithm, supplied by AstraZeneca ltd, 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/variant+calling+algorithm/variant+calling+algorithm/pmc04771182-25-16-18
    Average 90 stars, based on 1 article reviews
    variant calling algorithm - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Next-Generation Sequencing:

    Article Title: Acquired EGFR C797S mediates resistance to AZD9291 in advanced non-small cell lung cancer harboring EGFR T790M
    Article Snippet: We analyzed NGS data within the BCBio framework ( https://bcbio-nextgen.readthedocs.org/en/latest/ ) using an AstraZeneca-developed variant calling algorithm ( https://github.com/AstraZeneca-NGS/VarDict ).

    Variant Assay:

    Article Title: Acquired EGFR C797S mediates resistance to AZD9291 in advanced non-small cell lung cancer harboring EGFR T790M
    Article Snippet: We analyzed NGS data within the BCBio framework ( https://bcbio-nextgen.readthedocs.org/en/latest/ ) using an AstraZeneca-developed variant calling algorithm ( https://github.com/AstraZeneca-NGS/VarDict ).



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    Main characteristics of the studies included in the present systematic review.

    Journal: Diagnostics

    Article Title: The Need for Standardization in Next-Generation Sequencing Studies for Classic Hodgkin Lymphoma: A Systematic Review

    doi: 10.3390/diagnostics12040963

    Figure Lengend Snippet: Main characteristics of the studies included in the present systematic review.

    Article Snippet: ctDNA as a feasible strategy for genotyping and monitoring , Variants in SOCS1 (28%), IGLL5 (36%), TNFAIP3 (23%), GNA13 (23%) and STAT6 (21%). Poor prognosis features correlated with ctDNA concentration , VarScan2 and DGCaller algorithms for variant calling. RefSeq database for functional annotation , Illumina, San Diego, CA, USA , ctDNA , 60 cases of newly diagnosed cHL , Identify cHL somatic variants , Alcoceba et al., (2021) [ ] .

    Techniques: Sequencing, Software, Concentration Assay, Variant Assay, Functional Assay, Control, Biomarker Discovery, Isolation, Selection