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. Author manuscript; available in PMC: 2019 Apr 1.
Published in final edited form as: Curr Opin Genet Dev. 2018 Mar 23;49:70–78. doi: 10.1016/j.gde.2018.03.003

Table II.

Technological strategies for assessing satellite DNA

Platform Read length;
method
Pros Cons Example
Illumina Up to 300 bp; clustered amplicon Inexpensive, low error rate PCR bias in library prep*; short reads [40]
Ion torrent Up to 400 bp; on-bead amplicon Fast, inexpensive Lower yield; high error rate in homopolymer tracts [27]
Pacific Biosciences Up to 50 kb; single molecule Long reads; can assemble complex satellite regions Expensive; high error rate** [5]
Oxford Nanopore Up to 300 kb; single molecule Longest reads High error rate; extracting high molecular weight DNA is limiting Jain et al., bioRxiv 10.1101/170373
Optical mapping (nanochannel) Up to 220 kb; single molecule Long-range positional information; orthogonal method to sequencing Requires a reference genome; large nicking intervals preclude mapping simple sequences [41]
*

PCR-free libraries reduce bias.

**

PacBio also offers a Circular Consensus Sequencing (CSS) approach, where single circular molecules are read multiple times, thus generating a high quality consensus for each molecule.