Author

Sandra García‐Mulero

Institut d'Investigació Biomédica de BellvitgeORCID 0000-0003-4931-1267Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Josep Maria PiulatsiD· 2 shared Rebeca Sanz PamplonaiD· 2 shared Alena GrosiD· 1 shared Dietmar RiederiD· 1 shared Ferrán Moratalla-NavarroiD· 1 shared Jose Pedro VaqueiD· 1 shared L.P. del CarpioiD· 1 shared Mar VarelaiD· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenomics

Josep Maria PiulatsORCID

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2 papers

Recent·Most cited

GenomicsOncoImmunologyPeer-reviewedOct 24, 2023

Driver mutations in GNAQ and GNA11 genes as potential targets for precision immunotherapy in uveal melanoma patients

Sandra García‐Mulero, Roberto Fornelino, Marco Punta…·Rebeca Sanz Pamplona

The paper assesses the immunogenic potential of GNAQ and GNA11 mutations in uveal melanoma using genomic and transcriptomic data, finding Q209L mutations are more immunogenic than Q209P.

11 citations

humanbulk RNA-seq

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BioinformaticsbioRxivPreprintApr 27, 2020

Detection of Merkel cell polyomavirus using whole exome sequencing data

Sandra García‐Mulero, Ferrán Moratalla-Navarro, Soraya Curiel‐Olmo…·Josep Maria Piulats

The paper presents a bioinformatics method to detect Merkel cell polyomavirus insertions in whole exome sequencing data of Merkel cell carcinoma samples, achieving 100% sensitivity and 62.5% specificity.

2 citations

humanwhole-exome sequencing

𝕏 PostBluesky