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Genome Medicine
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May 29, 2020
The rate and spectrum of mosaic mutations during embryogenesis revealed by RNA sequencing of 49 tissues
Francesc Muyas, Luis Zapata, Roderic Guigó, et al.
BMC Methods
|
May 22, 2025
scAI-SNP: a method for inferring ancestry from single-cell data
Sung Chul Hong, Francesc Muyas, Isidro Cortés-Ciriano, et al.
Biorxiv : the Preprint Server for Biology
|
May 27, 2024
scAI-SNP: a method for inferring ancestry from single-cell data
Sung Chul Hong, Francesc Muyas, Isidro Cortés-Ciriano, et al.
Journal of Translational Medicine
|
August 27, 2025
GeneBits: ultra-sensitive tumour-informed ctDNA monitoring of treatment response and relapse in cancer patients
Julian Broche, Olga Kelemen, Aishwarya Sekar, et al.
Nature Biotechnology
|
July 6, 2023
De novo detection of somatic mutations in high-throughput single-cell profiling data sets
Francesc Muyas, Carolin M Sauer, Jose Espejo Valle-Inclán, et al.
Nature Communications
|
January 3, 2024
The ALT pathway generates telomere fusions that can be detected in the blood of cancer patients
Francesc Muyas, Manuel José Gómez Rodriguez, Rita Cascão, et al.
Plos Computational Biology
|
February 19, 2021
Efficient and flexible Integration of variant characteristics in rare variant association studies using integrated nested Laplace approximation
Hana Susak, Laura Serra-Saurina, German Demidov, et al.
Human Mutation
|
October 25, 2018
Allele balance bias identifies systematic genotyping errors and false disease associations
Francesc Muyas, Mattia Bosio, Anna Puig, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology
|
July 21, 2020
Dynamics of cell-free tumour DNA correlate with treatment response of head and neck cancer patients receiving radiochemotherapy
Franz J Hilke, Francesc Muyas, Jakob Admard, et al.
Human Mutation
|
April 27, 2019
eDiVA-Classification and prioritization of pathogenic variants for clinical diagnostics
Mattia Bosio, Oliver Drechsel, Rubayte Rahman, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 22) with videos related to
Sort By:
Page
of 3
Genome Medicine
|
May 29, 2020
The rate and spectrum of mosaic mutations during embryogenesis revealed by RNA sequencing of 49 tissues
Francesc Muyas, Luis Zapata, Roderic Guigó, et al.
BMC Methods
|
May 22, 2025
scAI-SNP: a method for inferring ancestry from single-cell data
Sung Chul Hong, Francesc Muyas, Isidro Cortés-Ciriano, et al.
Biorxiv : the Preprint Server for Biology
|
May 27, 2024
scAI-SNP: a method for inferring ancestry from single-cell data
Sung Chul Hong, Francesc Muyas, Isidro Cortés-Ciriano, et al.
Journal of Translational Medicine
|
August 27, 2025
GeneBits: ultra-sensitive tumour-informed ctDNA monitoring of treatment response and relapse in cancer patients
Julian Broche, Olga Kelemen, Aishwarya Sekar, et al.
Nature Biotechnology
|
July 6, 2023
De novo detection of somatic mutations in high-throughput single-cell profiling data sets
Francesc Muyas, Carolin M Sauer, Jose Espejo Valle-Inclán, et al.
Nature Communications
|
January 3, 2024
The ALT pathway generates telomere fusions that can be detected in the blood of cancer patients
Francesc Muyas, Manuel José Gómez Rodriguez, Rita Cascão, et al.
Plos Computational Biology
|
February 19, 2021
Efficient and flexible Integration of variant characteristics in rare variant association studies using integrated nested Laplace approximation
Hana Susak, Laura Serra-Saurina, German Demidov, et al.
Human Mutation
|
October 25, 2018
Allele balance bias identifies systematic genotyping errors and false disease associations
Francesc Muyas, Mattia Bosio, Anna Puig, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology
|
July 21, 2020
Dynamics of cell-free tumour DNA correlate with treatment response of head and neck cancer patients receiving radiochemotherapy
Franz J Hilke, Francesc Muyas, Jakob Admard, et al.
Human Mutation
|
April 27, 2019
eDiVA-Classification and prioritization of pathogenic variants for clinical diagnostics
Mattia Bosio, Oliver Drechsel, Rubayte Rahman, et al.
Page
of 3