|MoRFchibi SYSTEM: software tools for the identification of MoRFs in protein sequences|
N Malhis, M Jacobson, J Gsponer
Nucleic acids research 44 (W1), W488-W493, 2016
|LIST-S2: taxonomy based sorting of deleterious missense mutations across species|
N Malhis, M Jacobson, SJM Jones, J Gsponer
Nucleic acids research 48 (W1), W154-W161, 2020
|VariCarta: A comprehensive database of harmonized genomic variants found in autism spectrum disorder sequencing studies|
M Belmadani, M Jacobson, N Holmes, M Phan, T Nguyen, P Pavlidis, ...
Autism Research 12 (12), 1728-1736, 2019
|Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort|
DB Callaghan, S Rogic, PPC Tan, K Calli, Y Qiao, R Baldwin, M Jacobson, ...
Clinical genetics 96 (3), 199-206, 2019
|Curation of over 10 000 transcriptomic studies to enable data reuse|
N Lim, S Tesar, M Belmadani, G Poirier-Morency, BO Mancarci, ...
Database 2021, 2021
|Monitoring changes in the Gene Ontology and their impact on genomic data analysis|
M Jacobson, AE Sedeño-Cortés, P Pavlidis
GigaScience 7 (8), giy103, 2018
|GraPES: The Granule Protein Enrichment Server for prediction of biological condensate constituents|
ER Kuechler, M Jacobson, T Mayor, J Gsponer
Nucleic Acids Research, 2022
|Interactive Exploration, Analysis, and Visualization of Complex Phenome–Genome Datasets with ASPIREdb|
PPC Tan, S Rogic, A Zoubarev, C McDonald, F Lui, G Charathsandran, ...
Human mutation 37 (8), 719-726, 2016