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Table 1 The GeneCards suite member databases and tools

From: Rational confederation of genes and diseases: NGS interpretation via GeneCards, MalaCards and VarElect

Suite member title Type Brief description Relevant publication
GeneCards Affiliated database Human gene database Stelzer et al. (2016) The GeneCards suite: from gene data mining to disease genome sequence analysis, current protocols in bioinformatics [7]
MalaCards Affiliated database Human disease database Rappaport et al. MalaCards: an amalgamated human disease compendium with diverse clinical and genetic annotation and structured search, NAR [6]
PathCards Affiliated database Integrated human pathway database Belinky et al. PathCards: multi-source consolidation of human biological pathways, database [8]
GeneLoc Affiliated database Genome locator Rosen et al. GeneLoc: exon-based integration of human genome maps, bioinformatics [9]
LifeMap Affiliated database Embryonic development and stem cell compendium Buzhor et al. Cell-based therapy approaches: the hope for incurable diseases, future medicine [10]
TGex NGS analysis tool Knowledge-driven NGS analysis Stelzer G. et al. VarElect: the phenotype-based variation prioritizer of the GeneCards suite, BMC genomics [11]
VarElect NGS analysis tool NGS phenotyping Stelzer G. et al. VarElect: the phenotype-based variation prioritizer of the GeneCards suite, BMC genomics [11]
GeneAnalytics Analysis tool Gene set analysis Ben-Ari Fuchs et al. GeneAnalytics: an integrative gene set analysis tool, OMICS [12]
GenesLikeMe Analysis tool Related genes finder Stelzer et al. GeneDecks: paralog hunting and gene-set distillation with GeneCards annotation, OMICS [13]
GeneALaCart Analysis tool GeneCards batch queries Stelzer et al. In-silico human genomics with GeneCards, human genomics [4]