From: OmniMapFree: A unified tool to visualise and explore sequenced genomes
Data file | Type of Data Displayed |
---|---|
posn | Any feature with a position and size on a chromosome or scaffold. For example, genes, primer sequences, markers, homologous regions. Needs chromosome ID, start and end nucleotide positions. The first #-line of the data determines what colour is used to display this region. |
blast | Any sequence region identified in a blast search. Needs chromosome ID, start and end nucleotide positions and E-value. All data with E-values less than the E-value cut-off on the 2nd #-line of the data are displayed. |
expr | This allows different items in the same data file to be displayed in different colours. For example, with microarray expression data all up-regulated genes could be in red and all down-regulated genes in blue. The colour is determined by the last field on each data line. |
freq | This is used to display frequency data. For example, recombination frequency between genetic markers or %GC across a chromosome in a gradient of colours. The value of the last field on a data line is used to determine which of 20 user-defined colours are displayed. |
graph | This is used to draw a graph or histogram along a chromosome, for example SNP density. The value of the last field on a data line (e.g. number of SNPs/50,000 nt) is used to determine the y-value. |