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Shallow whole-genome sequencing of plasma cell-free DNA accurately differentiates small from non-small cell lung carcinoma.
- Published in:
- Genome Medicine, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s13073-020-00735-4
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- Publication type:
- Article
PREFACE: In silico pipeline for accurate cell-free fetal DNA fraction prediction.
- Published in:
- 2019
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- Publication type:
- journal article
Shallow whole-genome sequencing: a useful, easy to apply molecular technique for CNA detection on FFPE tumor tissue—a glioma-driven study.
- Published in:
- Virchows Archiv: European Journal of Pathology, 2022, v. 480, n. 3, p. 677, doi. 10.1007/s00428-022-03268-w
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- Publication type:
- Article
Detection of Copy Number Alterations by Shallow Whole-Genome Sequencing of Formalin-Fixed, Paraffin-Embedded Tumor Tissue.
- Published in:
- Archives of Pathology & Laboratory Medicine, 2020, v. 144, n. 8, p. 974, doi. 10.5858/arpa.2019-0010-OA
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- Publication type:
- Article
WisecondorX: improved copy number detection for routine shallow whole-genome sequencing.
- Published in:
- Nucleic Acids Research, 2019, v. 47, n. 4, p. 1605, doi. 10.1093/nar/gky1263
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- Publication type:
- Article
Application of an Ultrasensitive NGS-Based Blood Test for the Diagnosis of Early-Stage Lung Cancer: Sensitivity, a Hurdle Still Difficult to Overcome.
- Published in:
- Cancers, 2022, v. 14, n. 8, p. 2031, doi. 10.3390/cancers14082031
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- Publication type:
- Article