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High intensity sequencing of plasma cfDNA and WBC gDNA

We sought to define the technical feasibility of a high-intensity sequencing assay of cfDNA and matched white-blood cell (WBC) DNA covering a large genomic region (508 genes, 2Mb, 60,000x raw-depth) in a prospective study of 124 metastatic cancer patients, with contemporaneous matched metastatic tumor tissue biopsies, and age-matched 47 non-cancer controls.

Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data

Dataset ID Description Technology Samples
EGAD00001005302 396
Publications Citations
High-intensity sequencing reveals the sources of plasma circulating cell-free DNA variants.
Nat Med 25: 2019 1928-1937
325
Combining variant detection and fragment length analysis improves detection of minimal residual disease in postsurgery circulating tumour DNA of stage II-IIIA NSCLC patients.
Mol Oncol 16: 2022 2719-2732
11
Fragmentomic analysis of circulating tumor DNA-targeted cancer panels.
Ann Oncol 34: 2023 813-825
4
Aging clock based on nucleosome reorganisation derived from cell-free DNA.
Aging Cell 23: 2024 e14100
3