JSON

All terms in EDAM

Label Id Description
Pharmacogenomic test report data_1621 [A human-readable collection of information about the influence of genotype on drug response.]
EMBL feature format_1980 [EMBL feature format.]
GenBank feature format_1981 [Genbank feature format.]
ClustalW format format_1982 [ClustalW format for (aligned) sequences.]
markx10 format_1987 [Pearson MARKX10 alignment format.]
markx0 variant format_2922 [Some variant of Pearson MARKX alignment format.]
markx2 format_1988 [Pearson MARKX2 alignment format.]
markx3 format_1989 [Pearson MARKX3 alignment format.]
debug format_1983 [EMBOSS alignment format for debugging trace of full internal data content.]
FASTA-aln format_1984 [Fasta format for (aligned) sequences.]
markx0 format_1985 [Pearson MARKX0 alignment format.]
markx1 format_1986 [Pearson MARKX1 alignment format.]
Sequence image data_2969 [Image of a molecular sequence, possibly with sequence features or properties shown.]
Image data_2968 [Data (typically biological or biomedical) that has been rendered into an image, typically for display on screen.]
DNA-Seq topic_3177 [A topic concerning high-throughput sequencing of randomly fragmented genomic DNA, for example, to investigate whole-genome sequencing and resequencing, SNP discovery, identification of copy number variations and chromosomal rearrangements.]
Heat map data_1636 [A graphical 2D tabular representation of expression data, typically derived from an omics experiment. A heat map is a table where rows and columns correspond to different features and contexts (for example, cells or samples) and the cell colour represents the level of expression of a gene that context.]
Clustered expression profiles data_3768 [Groupings of expression profiles according to a clustering algorithm.]
DNA packaging topic_3176 [DNA-histone complexes (chromatin), organisation of chromatin into nucleosomes and packaging into higher-order structures.]
Structural variation topic_3175 [Variation in chromosome structure including microscopic and submicroscopic types of variation such as deletions, duplications, copy-number variants, insertions, inversions and translocations.]
Genetic variation topic_0199 [Stable, naturally occuring mutations in a nucleotide sequence including alleles, naturally occurring mutations such as single base nucleotide substitutions, deletions and insertions, RFLPs and other polymorphisms.]