Author

Antoni Castells

Hospital Clínic de BarcelonaORCID 0000-0001-8431-2033Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genomics· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:machine learning (classical)· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Approach:statistical model· 1

Frequent Co-Authors

Eva Hernández‐IllániD· 2 shared Jordi CampsiD· 2 shared Juan José LozanoiD· 2 shared Sergi Castellvı́-BeliD· 2 shared Albert de la ChapelleiD· 1 shared Amanda Ewart TolandiD· 1 shared Amanda Jane CrossiD· 1 shared Amit D. JoshiiD· 1 shared

Activity by Year

2019-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersGenomics

Eva Hernández‐IllánORCID

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3 papers

Recent·Most cited

GenomicsbioRxivPreprintApr 16, 2021

Copy-number intratumor heterogeneity contributes to predict relapse in chemotherapy-naive stage II colon cancer

Sara Lahoz, Iván Archilla, Elena Asensio…·Jordi Camps

The paper identifies copy-number intratumor heterogeneity as a predictor of relapse in stage II colon cancer, improving risk prediction beyond clinicopathological markers.

2 citations

humanbulk RNA-seq

𝕏 PostBluesky

Genetic & Genomic MedicineGutPeer-reviewedFeb 25, 2021

Genetic architectures of proximal and distal colorectal cancer are partly distinct

Jeroen R. Huyghe, Tabitha A. Harrison, Stephanie A. Bien…·Rachel Pearlman

This study identifies 13 new genetic loci specific to proximal or distal colorectal cancer subtypes, revealing partly distinct genetic architectures for these tumor locations.

80 citations

humanGWAS summary statistics

𝕏 PostBluesky

GenomicsbioRxivPreprintJul 16, 2019

CNApp: quantification of genomic copy number alterations in cancer and integrative analysis to unravel clinical implications

Sebastià Franch‐Expósito, Laia Bassaganyas, María Vila-Casadesús…·Jordi Camps

CNApp quantifies genomic copy number alterations in cancer and integrates them with clinical and molecular data to identify clinical implications.

DOI 10.1101/479667

humanwhole-genome sequencing

𝕏 PostBluesky