Stand-alone read mapping

Reads can be mapped to linear and circular chromosomes. Read mappings to circular genomes are visualized linearly as shown in figure 24.20.

Image mapping_circular_genome
Figure 24.20: Mapping reads to a circular chromosome. Reads that are marked with double arrows at the ends are reads that map across the starting point of the sequence. The arrows indicate that the alignment continues at the other end of the reference sequence.

Reads that map across the starting point of the sequence are shown both at the start and end of the reference sequence. Such reads are marked with » at the end of the read to indicate that the alignment continues at the other end of the reference sequence.

Mapping results can either be tracks (Image read_track_16_n_p) (see Tracks) or mapping tables (Image multicontig) or single mappings (Image contig). This section explains more about the latter two.

Note: If your read mapping or track shows the message 'Too much data for rendering' on a grey background, simply zoom in to see your reads in more detail. This occurs when there are too many reads to be displayed clearly. More specifically, where there are more than 500,000 reads displayed in a reads track, more than 200,000 reads displayed in a read mapping, or when the region being viewed in a read mapping is longer than 200,000 bases. Paired reads count as one in these cases.