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Adaptive Biotechnologies Corp next generation sequencing assay
Next Generation Sequencing Assay, supplied by Adaptive Biotechnologies Corp, 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/next+generation+sequencing+assay/immunoseq+platform/pmc13155964-177-16-20
Average 86 stars, based on 1 article reviews
next generation sequencing assay - by Bioz Stars, 2026-10
86/100 stars

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Related Articles

Variant Assay:

Article Title: Lymphoid malignancy and clonality in the POT1-mediated long telomere syndrome
Article Snippet: .. To further assess the B-cell repertoire in asymptomatic POT1 pathogenic variant carriers, we used a high-resolution next-generation sequencing assay (immunoSEQ; Adaptive Biotechnologies) to sample the variable CDR3 region of the immunoglobulin heavy chain gene ( IGH ). ..

Article Title: Lymphoid malignancy and clonality in the POT1-mediated long telomere syndrome.
Article Snippet: word count 250 Text word count 3965 Figure/table count 6 Reference count 56 D ow naded rom http://ashpublications.org/blood/art2/blood.2025031287/2499575/blood.2025031287.pdf by gest on 27 Jauary 2026

Next-Generation Sequencing:

Article Title: Lymphoid malignancy and clonality in the POT1-mediated long telomere syndrome
Article Snippet: .. To further assess the B-cell repertoire in asymptomatic POT1 pathogenic variant carriers, we used a high-resolution next-generation sequencing assay (immunoSEQ; Adaptive Biotechnologies) to sample the variable CDR3 region of the immunoglobulin heavy chain gene ( IGH ). ..

Article Title: Lymphoid malignancy and clonality in the POT1-mediated long telomere syndrome.
Article Snippet: word count 250 Text word count 3965 Figure/table count 6 Reference count 56 D ow naded rom http://ashpublications.org/blood/art2/blood.2025031287/2499575/blood.2025031287.pdf by gest on 27 Jauary 2026

Article Title: Early Chimeric Antigen Receptor T Cell Expansion Is Associated with Prolonged Progression-Free Survival for Patients with Relapsed/Refractory Multiple Myeloma Treated with Ide-Cel: A Retrospective Monocentric Study.
Article Snippet: The outcomes of patients with relapsed and refractory multiple myeloma (RRMM) previously treated with the 3 main classes of myeloma therapy—immunomodulatory drugs, proteasome inhibitors, and anti-CD38 antibodies—remain poor.. Recently, based on the phase II pivotal KarMMa trial showing prolonged overall survival (OS) and progressionfree survival (PFS) in heavily treated patients, idecabtagene vicleucel (ide-cel), a B cell maturation antigen (BCMA)-directed chimeric antigen receptor (CAR) T cell therapy (CAR-T) product, was approved in the United States for the treatment of RRMM.. In France, since June 2021, an early access program has authorized the use of ide-cel in the setting of RRMM (defined as progressive myeloma after at least 3 previous regimens, including the 3 main antimyeloma therapies).



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