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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]