Pacific bio sequences fall at other extreme from Illumina Solexa data. The reads are very long (~5kB), but they are also very noisy. Typically reads have 85% accuracy, which means every 100 nucleotides have 15 errors. Eeeks !!
We are just beginning, but let me walk through the experience so far step by step. You will receive the following files from the sequencer (X is some arbitrary file name) -
What are the files?
The top folder contains raw data in hd5 format, which is PacBio’s native data format. The sequencer also performs introductory analysis to generate some results, and those results are stored in Analysis_Results folder.
One important file in the Analysis_Results folder is x.ccs.fasta. This is the one you need to first look into oo gain some confidence into the generated data. Tt contains the cleanest assembled reads from the sequencing run. If you have a reference genome, you need to first align the ccs reads on to your reference genome. If that step fails, something went wrong with the sequencing run.
In our case, the size of ccs file is only 1% of the raw fasta sequence files. So, lot more sequences have not been included in ccs file, and to properly use them, you need to use SMRT software from PacBio. You will also find PacBioToCA tools useful.
Ideally one would like to run a de novo assembly with Pac Bio data, but that is very hard because of high error rate of the raw sequences. So, researchers are looking into two other possibilities -
i) Doing de novo assembly using Illumina or other short read technologies, and using PacBio to do scaffolding/extending,
ii) Running an error-correction routine on Pac Bio data using Illumina sequences, and then use those error-corrected reads for assembly. This is where PacBioToCA can help. For example, you can use Velvet to generate contigs from Pac Bio data, run error correction and then use error-corrected Pac Bio to improve Velvet assembly.
You may find the following resources handy for making further progress-