Resultados da busca - Huiwen Che
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1
Benchmarking of methods for DNA methylome deconvolution por Kobe De Ridder, Huiwen Che, Kaat Leroy, Bernard Thienpont
Publicado em 2024Artigo -
2
De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing Data por Adam Ameur, Huiwen Che, Marcel Martin, Ignas Bunikis, Johan Dahlberg, Ida Höijer, Susana Häggqvist, Francesco Vezzi, Jessica Nordlund, Pall I. Olason, Lars Feuk, Ulf Gyllensten
Publicado em 2018Artigo -
3
Noninvasive prenatal diagnosis by genome-wide haplotyping of cell-free plasma DNA por Huiwen Che, Darine Villela, Eftychia Dimitriadou, Cindy Melotte, Nathalie Brison, Maria Neofytou, Kris Van Den Bogaert, Olga Tšuiko, Koenraad Devriendt, Eric Legius, Masoud Zamani Esteki, Thierry Voet, Joris Vermeesch
Publicado em 2020Artigo -
4
Genomewide copy number alteration screening of circulating plasma DNA: potential for the detection of incipient tumors por Liesbeth Lenaerts, Peter Vandenberghe, Nathalie Brison, Huiwen Che, Maria Neofytou, Magali Verheecke, L. Leemans, Charlotte Maggen, Barbara Dewaele, Luc Dehaspe, Steven Vanderschueren, Daan Dierickx, Vincent Vandecaveye, Frédéric Amant, Joris Vermeesch
Publicado em 2018Artigo -
5
Breast Cancer Detection and Treatment Monitoring Using a Noninvasive Prenatal Testing Platform: Utility in Pregnant and Nonpregnant Populations por Liesbeth Lenaerts, Huiwen Che, Nathalie Brison, Maria Neofytou, Tatjana Jatsenko, Hanne Lefrère, Charlotte Maggen, Darine Villela, Magali Verheecke, Luc Dehaspe, Anca Croitor, Sigrid Hatse, Hans Wildiers, Patrick Neven, Vincent Vandecaveye, Giuseppe Floris, Joris Vermeesch, Frédéric Amant
Publicado em 2020Artigo -
6
Comprehensive genome-wide analysis of routine non-invasive test data allows cancer prediction: A single-center retrospective analysis of over 85,000 pregnancies por Liesbeth Lenaerts, Nathalie Brison, Charlotte Maggen, Leen Vancoillie, Huiwen Che, Peter Vandenberghe, Daan Dierickx, Lucienne Michaux, Barbara Dewaele, Patrick Neven, Giuseppe Floris, Thomas Tousseyn, Lore Lannoo, Tatjana Jatsenko, Isabelle Vanden Bempt, Kristel Van Calsteren, Vincent Vandecaveye, Luc Dehaspe, Koenraad Devriendt, Eric Legius, Kris Van Den Bogaert, Joris Vermeesch, Frédéric Amant
Publicado em 2021Artigo -
7
Genomic origin, fragmentomics, and transcriptional properties of long cell-free DNA molecules in human plasma por Huiwen Che, Peiyong Jiang, L Y Lois Choy, Suk Hang Cheng, Wenlei Peng, Rebecca W.Y. Chan, Jing Liu, Qing Zhou, W.K. Lam, Stephanie C Y Yu, So Ling Lau, Tak Yeung Leung, John Wong, Vincent Wai‐Sun Wong, Grace Lai‐Hung Wong, Stephen L. Chan, K.C. Allen Chan, Y. M. Dennis Lo
Publicado em 2024Artigo -
8
SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population por Adam Ameur, Johan Dahlberg, Pall I. Olason, Francesco Vezzi, Robert Karlsson, Marcel Martin, Johan Viklund, Andreas Kähäri, Pär Lundin, Huiwen Che, Jessada Thutkawkorapin, Jesper Eisfeldt, Samuel Lampa, Mats Dahlberg, Jonas Hagberg, Niclas Jareborg, Ulrika Liljedahl, Inger Jonasson, Åsa Johansson, Lars Feuk, Joakim Lundeberg, Ann‐Christine Syvänen, Sverker Lundin, Daniel Nilsson, Björn Nystedt, Patrik K. E. Magnusson, Ulf Gyllensten
Publicado em 2017Artigo
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Assuntos relacionados
Biology
Genetics
Gene
Genome
Cancer
Computational biology
Internal medicine
Medicine
Oncology
Copy number analysis
Copy-number variation
Demography
Gene expression
Genotype
Gynecology
Human genome
Malignancy
Obstetrics
Population
Pregnancy
Single-nucleotide polymorphism
Sociology
1000 Genomes Project
Algorithm
Benchmarking
Bioinformatics
Breast cancer
Business
Cancer research
Cell biology