PyPedia: using the wiki paradigm as crowd sourcing environment for bioinformatics protocols

por Kanterakis, Alexandros, Kuiper, Joël, Potamias, George, Swertz, Morris A.
Publicado 2015

The Hybrid Synthetic Microdata Platform: A Method for Statistical Disclosure Control

por Kuiper, Joël, van den Heuvel, Edwin R., Swertz, Morris A.
Publicado 2015

Road to FAIR genomes: a gap analysis of NGS data generation and sharing in the Netherlands

por Belien, Jeroen A M, Kip, Anke E, Swertz, Morris A
Publicado 2022

Neurodegenerative diseases: Lessons from genome-wide screens in small model organisms

por van Ham, Tjakko J, Breitling, Rainer, Swertz, Morris A, Nollen, Ellen A A
Publicado 2009

Semi-automatic translation of medicine usage data (in Dutch, free-text) from Lifelines COVID-19 questionnaires to ATC codes

por Kellmann, Alexander J, Lanting, Pauline, Franke, Lude, van Enckevort, Esther J, Swertz, Morris A
Publicado 2023

designGG: an R-package and web tool for the optimal design of genetical genomics experiments

por Li, Yang, Swertz, Morris A, Vera, Gonzalo, Fu, Jingyuan, Breitling, Rainer, Jansen, Ritsert C
Publicado 2009

Molgenis-impute: imputation pipeline in a box

por Kanterakis, Alexandros, Deelen, Patrick, van Dijk, Freerk, Byelas, Heorhiy, Dijkstra, Martijn, Swertz, Morris A
Publicado 2015

Consensus and conflict cards for metabolic pathway databases

por Stobbe, Miranda D, Swertz, Morris A, Thiele, Ines, Rengaw, Trebor, van Kampen, Antoine HC, Moerland, Perry D
Publicado 2013

The phenotypic spectrum of terminal and subterminal 6p deletions based on a social media-derived cohort and literature review

por Rraku, Eleana, Kerstjens-Frederikse, Wilhelmina S., Swertz, Morris A., Dijkhuizen, Trijnie, van Ravenswaaij-Arts, Conny M. A., Engwerda, Aafke
Publicado 2023

The Impact of Mode of Birth, and Episiotomy, on Postpartum Sexual Function in the Medium- and Longer-Term: An Integrative Systematic Review

por Fanshawe, Anne-Marie, De Jonge, Ank, Ginter, Nicole, Takács, Lea, Dahlen, Hannah G., Swertz, Morris A., Peters, Lilian L.
Publicado 2023

Worm variation made accessible: Take your shopping cart to store, link, and investigate!

por Snoek, L Basten, Joeri van der Velde, K, Li, Yang, Jansen, Ritsert C, Swertz, Morris A, Kammenga, Jan E
Publicado 2014

BiobankConnect: software to rapidly connect data elements for pooled analysis across biobanks using ontological and lexical indexing

por Pang, Chao, Hendriksen, Dennis, Dijkstra, Martijn, van der Velde, K Joeri, Kuiper, Joel, Hillege, Hans L, Swertz, Morris A
Publicado 2015

Single-cell RNA sequencing identifies cell type-specific cis-eQTLs and co-expression QTLs

por van der Wijst, Monique G.P., Brugge, Harm, de Vries, Dylan H., Deelen, Patrick, Swertz, Morris A., Franke, Lude
Publicado 2018

xQTL workbench: a scalable web environment for multi-level QTL analysis

por Arends, Danny, van der Velde, K. Joeri, Prins, Pjotr, Broman, Karl W., Möller, Steffen, Jansen, Ritsert C., Swertz, Morris A.
Publicado 2012

OntoCAT -- simple ontology search and integration in Java, R and REST/JavaScript

por Adamusiak, Tomasz, Burdett, Tony, Kurbatova, Natalja, Joeri van der Velde, K, Abeygunawardena, Niran, Antonakaki, Despoina, Kapushesky, Misha, Parkinson, Helen, Swertz, Morris A
Publicado 2011

Genotype harmonizer: automatic strand alignment and format conversion for genotype data integration

por Deelen, Patrick, Bonder, Marc Jan, van der Velde, K Joeri, Westra, Harm-Jan, Winder, Erwin, Hendriksen, Dennis, Franke, Lude, Swertz, Morris A
Publicado 2014

Bioinformatics tools and database resources for systems genetics analysis in mice—a short review and an evaluation of future needs

por Durrant, Caroline, Swertz, Morris A., Alberts, Rudi, Arends, Danny, Möller, Steffen, Mott, Richard, Prins, Pjotr, van der Velde, K. Joeri, Jansen, Ritsert C., Schughart, Klaus
Publicado 2012

WormQTL(HD)—a web database for linking human disease to natural variation data in C. elegans

por van der Velde, K. Joeri, de Haan, Mark, Zych, Konrad, Arends, Danny, Snoek, L. Basten, Kammenga, Jan E., Jansen, Ritsert C., Swertz, Morris A., Li, Yang
Publicado 2014

Feasibility of predicting allele specific expression from DNA sequencing using machine learning

por Zhang, Zhenhua, van Dijk, Freerk, de Klein, Niek, van Gijn, Mariëlle E, Franke, Lude H, Sinke, Richard J, Swertz, Morris A, van der Velde, K Joeri
Publicado 2021

Complex nature of SNP genotype effects on gene expression in primary human leucocytes

por Heap, Graham A, Trynka, Gosia, Jansen, Ritsert C, Bruinenberg, Marcel, Swertz, Morris A, Dinesen, Lotte C, Hunt, Karen A, Wijmenga, Cisca, vanHeel, David A, Franke, Lude
Publicado 2009