دورية أكاديمية

Capture-based targeted sequencing using a T-cell control in myeloid malignancies and idiopathic cytopenias

التفاصيل البيبلوغرافية
العنوان: Capture-based targeted sequencing using a T-cell control in myeloid malignancies and idiopathic cytopenias
المؤلفون: Pietka, Grzegorz, De Lord, Corinne, Matthias, Gwynn, Cheung, Betty, Atwal, Sangeeta, Furtado, Michelle, Cullis, Jonathan, Grey-Davies, Liz, Narayanan, Srinivasan, McGregor, Andrew, Kilner, Mari, Bosworth, Jenny, McMullin, Mary Frances, Coats, Thomas, Parcharidou, Agapi, Cavenagh, Jamie, Byrne, Jenny, Iyengar, Sunil, Mohammed, Kabir, Cross, Nicholas, Hubank, Mike, Ribeiro, Sara, Khorashad, Jamshid, Wren, Dorte, O'Connor, Simon, Taussig, David
المصدر: Pietka , G , De Lord , C , Matthias , G , Cheung , B , Atwal , S , Furtado , M , Cullis , J , Grey-Davies , L , Narayanan , S , McGregor , A , Kilner , M , Bosworth , J , McMullin , M F , Coats , T , Parcharidou , A , Cavenagh , J , Byrne , J , Iyengar , S , Mohammed , K , Cross , N , Hubank , M , Ribeiro , S , Khorashad , J , Wren , D , O'Connor ....
سنة النشر: 2024
المجموعة: Queen's University Belfast: Research Portal
مصطلحات موضوعية: Hematology
الوصف: We report on a study of next-generation sequencing in 257 patients undergoing investigations for cytopenias. We sequenced bone marrow aspirates using a target enrichment panel comprising 82 genes and used T cells from paired blood as a control. One hundred and sixty patients had idiopathic cytopenias, 81 had myeloid malignancies and 16 had lymphoid malignancies or other diagnoses. Forty-seven of the 160 patients with idiopathic cytopenias had evidence of somatic pathogenic variants consistent with clonal cytopenias. Only 39 genes of the 82 tested were mutated in the 241 patients with either idiopathic cytopenias or myeloid neoplasms. We confirm that T cells can be used as a control to distinguish between germline and somatic variants. The use of paired analysis with a T-cell control significantly reduced the time molecular scientists spent reporting compared to unpaired analysis. We identified somatic variants of uncertain significance (VUS) in a higher proportion (24%) of patients with myeloid malignancies or clonal cytopenias compared to less than 2% of patients with non-clonal cytopenias. This suggests that somatic VUS are indicators of a clonal process. Lastly, we show that blood depleted of lymphocytes can be used in place of bone marrow as a source of material for sequencing.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
العلاقة: https://pure.qub.ac.uk/en/publications/21505c3c-3208-4f92-8e32-c50a783fd667Test
DOI: 10.1111/bjh.19377
الإتاحة: https://doi.org/10.1111/bjh.19377Test
https://pure.qub.ac.uk/en/publications/21505c3c-3208-4f92-8e32-c50a783fd667Test
https://pureadmin.qub.ac.uk/ws/files/565052019/Br_J_Haematol_-_2024_-_Pietka_-_Capture_based_targeted_sequencing_using_a_T_cell_control_in_myeloid_malignancies_and.pdfTest
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.1DBDEF39
قاعدة البيانات: BASE