Marcel Martin

Researcher Next ID · RN-025445

Researcher · Biochemistry, Genetics and Molecular Biology

Stockholm University

Stockholm, Sweden

Not currently recruitingFunding unknown

Works count: 74
Citation count: 41,803
H-index: 31
i10-index: 44

Research interests

Biochemistry, Genetics and Molecular Biology

Genomics and Phylogenetic Studies

Genomics and Rare Diseases

RNA modifications and cancer

Cancer Genomics and Diagnostics

RNA and protein synthesis mechanisms

Publications

Sarek: A portable workflow for whole-genome sequencing analysis of germline and somatic variants
F1000Research · 2020 · https://doi.org/10.12688/f1000research.16665.2
SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population
European Journal of Human Genetics · 2017 · https://doi.org/10.1038/ejhg.2017.130
Atropos: specific, sensitive, and speedy trimming of sequencing reads
PeerJ · 2017 · https://doi.org/10.7717/peerj.3720
Computational Pan-Genomics: Status, Promises and Challenges
bioRxiv (Cold Spring Harbor Laboratory) · 2016 · https://doi.org/10.1101/043430
Computational pan-genomics: status, promises and challenges
Briefings in Bioinformatics · 2016 · https://doi.org/10.1093/bib/bbw089
Production of individualized V gene databases reveals high levels of immunoglobulin genetic diversity
Nature Communications · 2016 · https://doi.org/10.1038/ncomms13642
The genetic basis for ecological adaptation of the Atlantic herring revealed by genome sequencing
eLife · 2016 · https://doi.org/10.7554/elife.12081
Cloche is a bHLH-PAS transcription factor that drives haemato-vascular specification
Nature · 2016 · https://doi.org/10.1038/nature18614
WhatsHap: fast and accurate read-based phasing
bioRxiv (Cold Spring Harbor Laboratory) · 2016 · https://doi.org/10.1101/085050
Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3
Nature Genetics · 2013 · https://doi.org/10.1038/ng.2674
A comprehensive molecular study on Coffin–Siris and Nicolaides–Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling
Human Molecular Genetics · 2013 · https://doi.org/10.1093/hmg/ddt366
Cutadapt removes adapter sequences from high-throughput sequencing reads
EMBnet journal · 2011 · https://doi.org/10.14806/ej.17.1.200
Deep sequencing reveals differential expression of microRNAs in favorable versus unfavorable neuroblastoma
Nucleic Acids Research · 2010 · https://doi.org/10.1093/nar/gkq342

Current projects

No projects listed.