In this phase we received two sets of refined sequences. The sequences in these sets come from sequences, which we've been denoting as Kruger and Wittiya sequences. Posts on this blog hereupon will be referencing these new data sets unless noted otherwise.
The sequences are already aligned using multiple sequence alignment and the we name the two data sets as 599Nts and 999Nts as they contain 599 and 999 base spans respectively in the aligned form. Total number of sequences in these sets are,
The sequences are already aligned using multiple sequence alignment and the we name the two data sets as 599Nts and 999Nts as they contain 599 and 999 base spans respectively in the aligned form. Total number of sequences in these sets are,
- 599Nts -- 1821 sequences
- 999Nts -- 1306 sequences
The description we received from our collaborators on this data is (copied from email conversation with Geoffrey House and modified for blog) is given below on the right with the graph.
We created the full sequence data set (for the large subunit (LSU) sequences only) by taking the aligned sequences that were used in Kruger et al 2012 (and that were 400-1300 bp long), and adding Wittaya's sequences to the existing alignment using MAFFT and its --add option.
We then made line graphs of the number of sequences that contained a base at each sequence position The top panel is the sequence coverage of the combined data set (Kruger and Wittaya), the middle panel graphs the sequence coverage of only the Kruger sequences within the combined data set, and the bottom panel graphs the sequence coverage of only the Wittaya sequences within the combined data set.
From the graphs, we saw that a large number of sequences contained nucleotides along a 999 base span. Even more sequences contained nucleotides along a 499 base span that was nested within the 999 base span. The red rectangles above the top panel of the graph to denote the approximate sequence locations of these two different base length spans.
This is how we derived the two sets of sequences - one is all of the sequences that span the 499 bases, and the other is all of the sequences that span the 999 bases (which essentially represents a subset of the sequences spanning the 499 base length).
Finally for adding Wittaya's sequences to Kruger's, we used the default alignment option in MAFFT, which is very fast but possibly a bit rough. It is possible that we may need to slightly refine the MAFFT alignments later in the project to improve their accuracy, but that should have a fairly small effect on the length of the aligned sequences.
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